Marfan syndrome (genetic disorder of the connective tissue)

main subject (P921)

Q59217640	1039 Prevalence of cardiovascular manifestations in patients with Marfan syndrome: a cardiovascular magnetic resonance study
Q57744014	108 4D-flow CMR demonstrates the regional distribution of aortic flow disturbance in Marfan syndrome
Q70659790	16 cases of scoliosis--Marfan's syndrome
Q48383709	1997 Albert Lasker Award for Special Achievement in Medical Science. Observations over 50 years concerning intestinal polyposis, Marfan syndrome and achondroplasia
Q43007212	2006 Curt Stern Award Address. Marfan syndrome: from molecules to medicines
Q49130602	5B.05: MARFAN SYNDROME: ASSESSMENT OF AORTIC DISSECTION RISK BY ANALYSIS OF AORTIC VISCOELASTIC PROPERTIES.
Q48867717	A 10-year-old boy with Marfan syndrome exhibiting cerebrovascular abnormalities.
Q80361187	A 12 year old with scoliosis. Marfan syndrome
Q81342201	A 27-year-old man with Marfan syndrome and "tearing" nonradiating chest pain
Q70083152	A 38 base pair insertion in the pro alpha 2(I) collagen gene of a patient with Marfan syndrome
Q57994548	A Case Report of Expanding Abdominal Aneurysm and Annuloectasia in Marfan Syndrome
Q42327967	A Case of Neonatal Marfan Syndrome: A Management Conundrum and the Role of a Multidisciplinary Team
Q90219795	A Case of an Abdominal Aortic Dissection in a Hemodynamically Stable Marfan Syndrome Patient Presenting without Pain
Q58589667	A FBN1 3'UTR mutation variant is associated with endoplasmic reticulum stress in aortic aneurysm in Marfan syndrome
Q39647773	A FBN1 mutation association with different phenotypes of Marfan syndrome in a Chinese family
Q92421703	A Giant Tarlov Cyst Presenting with Hydronephrosis in a Patient with Marfan Syndrome: A Case Report and Review of the Literature
Q61480597	A Major Involvement of the Cardiovascular System in Patients Affected by Marfan Syndrome: Novel Mutations in Fibrillin 1 Gene
Q33298689	A Marfan syndrome gene expression phenotype in cultured skin fibroblasts
Q41934843	A Marfan syndrome human induced pluripotent stem cell line with a heterozygous FBN1 c.4082G>A mutation, ISMMSi002-B, for disease modeling
Q93183572	A Novel Case of Marfan Syndrome in an Infant With Hypoplastic Left Heart Syndrome
Q49100465	A Novel Fibrillin-1 Gene Mutation Leading to Marfan Syndrome in a Korean Girl.
Q47332270	A Novel Murine Model of Marfan Syndrome Accelerates Aortopathy and Cardiomyopathy
Q92580632	A Review of Psychosocial Factors of Marfan Syndrome: Adolescents, Adults, Families, and Providers
Q51683195	A Woman With Marfan Syndrome in Pregnancy: Managing High Vascular Risk With Multidisciplinary Care.
Q80976079	A bioinformatics framework for genotype-phenotype correlation in humans with Marfan syndrome caused by FBN1 gene mutations
Q95589173	A c.3037G>A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype
Q90557692	A case of G1013R FBN1 mutation: A potential genotype-phenotype correlation in severe Marfan syndrome
Q72122708	A case of Marfan syndrome associated with glaucoma
Q44355369	A case of Marfan syndrome associated with hydronephrosis and aneurysmatic bone cyst
Q73169199	A case of Marfan syndrome in an adolescent with aortic dissection: should the recommendation for surgical intervention be changed?
Q42431508	A case of Marfan syndrome with acute monoblastic leukemia
Q92501286	A case of Marfan syndrome with massive haemoptysis from collaterals of the lateral thoracic artery
Q87190073	A case of acute aortic dissection in a woman with Marfan syndrome at 29 weeks' gestation
Q72830797	A case of coronary anastomotic aneurysm 5 years after Bentall procedure in Marfan syndrome
Q51674682	A case of hypoparathyroidism combined with Marfan syndrome in a 20-year-old female.
Q84589275	A case of neonatal Marfan syndrome with good late follow-up: is it possible to avoid an early unfavourable outcome?
Q44430334	A case of the Marfan syndrome in an old lady of 72 with marked cardiovascular involvement
Q42100551	A case of the thoracic aneurysm due to medionecrosis without Marfan syndrome (author's transl)
Q45248165	A case presenting concurrence of Marfan syndrome, Basedow's disease and Arg353Gln polymorphism-related factor VII deficiency
Q68472024	A case report of idiopathic SIADH coincident with Marfan syndrome associated with sick sinus syndrome and chronic pulmonary emphysema
Q57577758	A comparison of the ghent and revised ghent nosologies for the diagnosis of marfan syndrome in an adult korean population
Q84006785	A huge noncoronary sinus of Valsalva aneurysm in a patient with Marfan syndrome
Q33593705	A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an International Consortium study.
Q86560217	A marked decrease in heart rate variability in Marfan syndrome patients with confirmed FBN1 mutations
Q81344366	A metatarsal equivalent to the metacarpal index in Marfan syndrome
Q41373533	A microfibril assembly assay identifies different mechanisms of dominance underlying Marfan syndrome, stiff skin syndrome and acromelic dysplasias
Q33770305	A new mouse model for marfan syndrome presents phenotypic variability associated with the genetic background and overall levels of Fbn1 expression
Q35680230	A new novel mutation in FBN1 causes autosomal dominant Marfan syndrome in a Chinese family
Q78347982	A new on-line method for predicting aortic root dilatation during two-dimensional echocardiography in pediatric patients with Marfan syndrome using the sinus of valsalva to annulus ratio
Q35779276	A nonsense mutation in the fibrillin-1 gene of a Marfan syndrome patient induces NMD and disrupts an exonic splicing enhancer
Q100760312	A nonsense variant in FBN1 caused autosomal dominant Marfan syndrome in a Chinese family: a case report
Q87293238	A novel FBN1 heterozygous mutation identified in a Chinese family with autosomal dominant Marfan syndrome
Q77866990	A novel G to A substitution at nucleotide 1734 of the FBN1 gene predicting a C534Y mutation responsible for marfan syndrome
Q34299873	A novel fibrillin 1 gene mutation leading to marfan syndrome with minimal cardiac features.
Q70742944	A novel fibrillin mutation in the Marfan syndrome which could disrupt calcium binding of the epidermal growth factor-like module
Q36006511	A novel fibrillin-1 gene missense mutation associated with neonatal Marfan syndrome: a case report and review of the mutation spectrum.
Q64052088	A novel mutation in FBN1 gene in autosomal dominant Marfan syndrome and macular degeneration in a Chinese consanguineous family
Q73493287	A novel mutation in the neonatal region of the fibrillin (FBN)1 gene associated with a classical phenotype of Marfan syndrome (MfS). Mutations in brief no. 163. Online
Q97534033	A novel splicing mutation in Marfan syndrome
Q71711566	A point mutation creating an extra N-glycosylation site in fibrillin-1 results in neonatal Marfan syndrome
Q45876290	A possible advance in arterial gene therapy for aortic complications in the Marfan syndrome by local transfer of an antisense Mg-dependent hammerhead ribozyme.
Q71597099	A prospective longitudinal evaluation of pregnancy in the Marfan syndrome
Q34455509	A prospective, randomized, placebo-controlled, double-blind, multicenter study of the effects of irbesartan on aortic dilatation in Marfan syndrome (AIMS trial): study protocol.
Q36544464	A prospectus on the prevention of aortic rupture in the Marfan syndrome with data on survivorship without treatment
Q78364589	A quantitative abnormality in serum mucoproteins in the Marfan syndrome
Q45781057	A rare case of Marfan syndrome and concomitant alpha-1 antitrypsin deficiency
Q38702972	A re-operative case of bentall operation and aortic arch replacement using a stent graft for a Marfan syndrome, post sternum turnover and post mitral valve replacement
Q104265002	A reimplantation valve-sparing root replacement (T. David-V) and aortic valve repair procedure in a patient with Marfan syndrome
Q79422635	A report of the successful surgical treatment of aortic regurgitation from a dissecting aortic aneurysm in a patient with the Marfan syndrome
Q92908492	A scoping review presenting a wide variety of research on paediatric and adolescent patients with Marfan syndrome
Q100571383	A seX(X/Y) Article on Marfan Syndrome
Q36099630	A second locus for Marfan syndrome maps to chromosome 3p24.2-p25.
Q56988676	A simple clinical model to estimate the probability of Marfan syndrome
Q72850096	A simple screening test for the Marfan syndrome
Q39682429	A suggestion of linkage between the Marfan syndrome and the rhesus blood group
Q96613517	A synonymous mutation in exon 39 of FBN1 causes exon skipping leading to Marfan syndrome
Q89075824	A systemic review and meta-analysis: long-term results of the Bentall versus the David procedure in patients with Marfan syndrome
Q84609501	A teenager with Marfan syndrome and left ventricular noncompaction
Q75315507	A true aneurysm of axillary-subclavian artery with cystic medionecrosis: an unusual manifestation of Marfan syndrome
Q68022792	A unique association of Marfan syndrome with craniofacial hypoplasia, oligophrenia and severe microphthalmia
Q41668761	A workshop on Marfan syndrome, 10 June 1989, Farmington, CT, USA.
Q73628595	AAP: health supervision for children with Marfan syndrome
Q46699974	AB081. Variable major phenotypes in familial Marfan syndrome in Indonesia: a case report.
Q76786105	ABSENCE OF THE PULMONARY VALVE. A CASE OCCURRING IN THE MARFAN SYNDROME
Q35515879	ADAMTSL6β protein rescues fibrillin-1 microfibril disorder in a Marfan syndrome mouse model through the promotion of fibrillin-1 assembly.
Q43117594	AT1 receptor antagonism to reduce aortic expansion in Marfan syndrome: lost in translation or in need of different interpretation?
Q60637249	Abdominal Aortic Dilatation During Pregnancy in Marfan Syndrome
Q80097033	Abdominal aortic dissection with acute mesenteric ischemia in a patient with Marfan syndrome
Q73933446	Abnormal extracellular matrix protein transport associated with increased apoptosis of vascular smooth muscle cells in marfan syndrome and bicuspid aortic valve thoracic aortic aneurysm
Q48111133	Abnormal heart rate recovery and deficient chronotropic response after submaximal exercise in young Marfan syndrome patients.
Q52986101	Abnormal origin and interarterial course of coronary arteries in Marfan syndrome: CT coronary angiography features.
Q59026290	Abraham Lincoln and Marfan syndrome
Q57282777	Absence of LTBP-3 attenuates the aneurysmal phenotype but not spinal effects on the aorta in Marfan syndrome
Q71869726	Absorption Pharmacokinetics of Atenolol in Patients with the Marfan Syndrome
Q91618153	Accelerated Marfan syndrome model recapitulates established signaling pathways
Q69089075	Acetabular protrusion in the Marfan syndrome
Q95627042	Acroangiodermatitis (Pseudo-Kaposi's Sarcoma) Seen in Conjunction with Marfan Syndrome and a Hypercoagulable State: Is There a Link?
Q89412129	Acute Eye Pain Following Prolonged Face-Down Positioning in a Patient With Marfan Syndrome
Q87208522	Acute aortic dissection after caesarean section in a patient with Marfan syndrome
Q92250819	Acute aortic dissection in a patient with Marfan syndrome during advanced pregnancy
Q36495863	Acute aortic dissection in pregnancy in a woman with undiagnosed marfan syndrome
Q34148297	Acute aortic dissection in pregnancy with the marfan syndrome
Q41975617	Acute aortic dissection mimics acute inferoposterior wall myocardial infarction in a Marfan syndrome patient.
Q86631127	Acute coronary involvement in acute type A aortic dissection: a subgroup analysis of bicuspid aortic valve and Marfan syndrome
Q47711915	Acute coronary syndrome in a patient with Marfan syndrome following emergent surgical repair of aortic dissection.
Q78110016	Acute mitral regurgitation due to chordal rupture in a patient with neonatal Marfan syndrome caused by a deletion in exon 29 of the FBN1 gene
Q50455688	Acute myeloblastic leukemia-associated Marfan syndrome and Davidoff-Dyke-Masson syndrome: a case report.
Q83740536	Acute subdural hematoma following thoracoabdominal aortic repair in a patient with Marfan syndrome: a rare complication of cerebrospinal fluid drainage
Q91591198	Adult Patients With Marfan Syndrome and Ascending Aortic Surgery
Q87393755	Afferent signaling impairment from baroreceptors cannot fully explain decrease in heart rate variability in Marfan syndrome patients: an author's reply
Q55129001	Age Differences in Axial Length, Corneal Curvature, and Corneal Astigmatism in Marfan Syndrome with Ectopia Lentis.
Q84563200	Age-related and regional changes of aortic stiffness in the Marfan syndrome: assessment with velocity-encoded MRI
Q73473315	Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of italian families with Marfan syndrome
Q73802570	Allelic variation in normal human FBN1 expression in a family with Marfan syndrome: a potential modifier of phenotype?
Q30842225	Altered aortic 3D hemodynamics and geometry in pediatric Marfan syndrome patients.
Q77213882	Alternative splicing of exon 37 of FBN1 deletes part of an 'eight-cysteine' domain resulting in the Marfan syndrome
Q36875872	Ambulatory (24 h) blood pressure and arterial stiffness measurement in Marfan syndrome patients: a case control feasibility and pilot study
Q90145332	An Endoscopic Solution to Mitral Regurgitation in a Complex Patient With Marfan Syndrome
Q44281051	An FBN1 pseudoexon mutation in a patient with Marfan syndrome: confirmation of cryptic mutations leading to disease
Q38258800	An Overlap Syndrome of Pigment Dispersion and Pigmentary Glaucoma accompanied by Marfan Syndrome: Case Report with Literature Review
Q83178678	An alternative surgical approach for the combined treatment of pectus excavatum and acute aortic dissection type-A in Marfan syndrome
Q67909225	An autopsy case of Marfan syndrome with bronchiectasis and multiple bullae
Q72837442	An autopsy case of Marfan syndrome with histochemical studies on the cardiovascular system
Q98946475	An enormous Italian pedigree of Marfan syndrome with a novel mutation in the FBN1 gene
Q83767147	An evidence-based hypothesis for beneficial effects of telmisartan on Marfan syndrome
Q33597148	An exclusion map of Marfan syndrome
Q48194218	An iPSC-derived vascular model of Marfan syndrome identifies key mediators of smooth muscle cell death
Q47920453	An integrated approach to management of Marfan syndrome caused by an FBN1 exon 18 mutation in an Australian Aboriginal family.
Q86628456	An unclassified viariant in the fibrillin-1 gene leading to exon skipping in a patient with Marfan syndrome: the use of minigene assay in splicing analysis
Q94523110	An uncommon case of thunderclap headache in a patient with Marfan syndrome
Q57150086	AnFBN1Deep Intronic Mutation in a Familial Case of Marfan Syndrome: An Explanation for Genetically Unsolved Cases?
Q36007830	Analysis of Protrusio Acetabuli Using a CT-based Diagnostic Method in Korean Patients with Marfan Syndrome: Prevalence and Association with Other Manifestations.
Q59237749	Analysis of the fibrillin-1 gene (FBN1) in patients with Marfan syndrome
Q92554009	Anatomically specific reactive oxygen species production participates in Marfan syndrome aneurysm formation
Q100571376	Androgens Accentuate TGF-β Dependent Erk/Smad Activation During Thoracic Aortic Aneurysm Formation in Marfan Syndrome Male Mice
Q92862261	Anesthetic management for cesarean section and tubal ligation in a patient with Marfan syndrome, multiple sclerosis, and multiple postdural puncture headaches
Q48185427	Anesthetic management of a child with both Marfan syndrome and Turner syndrome.
Q37382032	Anesthetic management of a patient with Marfan syndrome and severe aortic root dilatation undergoing cholecystectomy and partial hepatic resection
Q43602698	Anesthetic management of parturients with Marfan syndrome
Q51058253	Aneurysm of the renal artery in a patient with the Marfan syndrome, treated by stenting and coils implantation.
Q38274806	Aneurysmal dilatation of the aortic sinuses of Valsalva -- beyond Marfan syndrome: a single centre experience and review of the literature.
Q87155587	Aneurysms of medium-sized arteries in Marfan syndrome
Q38256653	Angiotensin receptor blockers: a panacea for Marfan syndrome and related disorders?
Q55266983	Angiotensin, transforming growth factor β and aortic dilatation in Marfan syndrome: Of mice and humans.
Q91969024	Angiotensin-II receptor blockade in Marfan syndrome
Q82733263	Annuloaortic ectasia treated successfully in a pregnant woman with Marfan syndrome: report of a case
Q82786149	Anomalous aortic origin of a coronary artery in siblings with Marfan syndrome
Q44778500	Antagonism of GxxPG fragments ameliorates manifestations of aortic disease in Marfan syndrome mice
Q40895293	Anterior sacral meningocele and Marfan syndrome: a review
Q73649625	Anterior sacral meningocele as a pelvic complication of Marfan syndrome
Q73816064	Anterior sacral meningocele in a patient with Marfan syndrome
Q72871567	Anterior sacral meningocele presenting as a pelvic/abdominal mass in a patient with Marfan syndrome
Q89542147	Anterior spinal artery syndrome from type A aortic dissection in a patient with Marfan syndrome due to a novel fibrillin mutation
Q85041896	Anthropometric and musculoskeletal assessment of patients with Marfan syndrome
Q87950413	Aortic Arch in Marfan Syndrome Repaired Using the XL-stent
Q37240515	Aortic Complications Associated With Pregnancy in Marfan Syndrome: The NHLBI National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC).
Q90564875	Aortic Complications in Marfan Syndrome: Should We Anticipate Preventive Aortic Root Surgery?
Q38351248	Aortic Involvement in Pediatric Marfan syndrome: A Review
Q49035192	Aortic Root Dilation: Do Patients With Marfan Syndrome Fare Worse Than Those With Marfanoid Features?
Q91857630	Aortic Root Replacement and Berlin Heart EXCOR Implantation in Marfan Syndrome
Q38763643	Aortic Root Surgery in Marfan Syndrome: Medium-Term Outcome in a Single-Center Experience
Q57051845	Aortic Surgery Outcomes of Marfan Syndrome and Ehlers-Danlos Syndrome Patients at Teaching and Non-Teaching Hospitals
Q84633292	Aortic Valve Sparing Procedure Combined with Sternal Turnover for Marfan Syndrome
Q95400824	Aortic aneurysm and non-Hodgkin's lymphoma in Marfan syndrome
Q37840361	Aortic aneurysm with valvular insufficiency: is it due to Marfan syndrome or hypertension? A case report and review of literature
Q70574025	Aortic biomechanical properties in pediatric patients with the Marfan syndrome, and the effects of atenolol
Q43530803	Aortic biomechanics by magnetic resonance: early markers of aortic disease in Marfan syndrome regardless of aortic dilatation?
Q50789978	Aortic diameter predicts acute type A aortic dissection in patients with Marfan syndrome but not in patients without Marfan syndrome.
Q47324509	Aortic dilatation in Marfan syndrome: role of arterial stiffness and fibrillin-1 variants
Q54569289	Aortic dilatation patterns and rates in adults with bicuspid aortic valves: a comparative study with Marfan syndrome and degenerative aortopathy.
Q46048027	Aortic disease in patients with Marfan syndrome: aortic volume assessment for surveillance.
Q91660095	Aortic dissection during pregnancy and postpartum in patients with Marfan syndrome: a 21-year clinical experience in 30 patients
Q47116707	Aortic dissection in patients with Marfan syndrome based on the IRAD data
Q39464795	Aortic events in a nationwide Marfan syndrome cohort
Q57991085	Aortic flow patterns in patients with Marfan syndrome assessed by flow-sensitive four-dimensional MRI
Q92202739	Aortic imaging and biomechanics in Marfan syndrome: keep it simple but not too simple
Q39900055	Aortic insufficiency in a patient with Marfan syndrome after aortic root reconstruction with a tailored-sinus graft.
Q43711868	Aortic insufficiency in patients with Marfan syndrome: a surgical dilemma.
Q36572967	Aortic lesion in Marfan syndrome: the ultrastructure of cystic medial degeneration
Q69570360	Aortic regurgitation in a young girl with severe form of Marfan syndrome
Q89155958	Aortic repair in Marfan syndrome: Let's not forget the arch when talking about the root
Q90761274	Aortic root aneurysms in a child with Marfan syndrome
Q100462465	Aortic root dilation in a child with Marfan syndrome and mosaic Turner syndrome
Q44327346	Aortic root operations for Marfan syndrome: a comparison of the Bentall and valve-sparing procedures
Q51347334	Aortic root pathology in Marfan syndrome increases the risk of migraine with aura.
Q51296152	Aortic root reconstruction by aortic valve-sparing operation (David type I reimplantation) in Marfan syndrome accompanied by annuloaortic ectasia and acute type-A aortic dissection.
Q81314282	Aortic root surgery in Marfan syndrome
Q83490783	Aortic root surgery in Marfan syndrome
Q100638119	Aortic root surgery in Marfan syndrome
Q84618395	Aortic root surgery in Marfan syndrome: Bentall procedure with the composite mechanical valved conduit versus David reimplantation with the Valsalva graft
Q45128740	Aortic root surgery in Marfan syndrome: Bentall procedure with the composite mechanical valved conduit versus aortic valve reimplantation with Valsalva graft
Q75412845	Aortic root surgery in Marfan syndrome: Comparison of aortic valve-sparing reimplantation versus composite grafting
Q41577607	Aortic root surgery in Marfan syndrome: current practice and evolving techniques
Q88441167	Aortic stiffness in adolescent Turner and Marfan syndrome patients
Q73508903	Aortic surgery in patients with marfan syndrome: long-term survival, morbidity and function
Q53538073	Aortic tear and dissection related to connective tissues abnormalities resembling Marfan syndrome in a Great Dane.
Q36127215	Aortic valve avulsion after proximal aortic dissection in the Marfan syndrome: echocardiographic features and management
Q72427399	Aortic valve repair in patients with Marfan syndrome and ascending aorta aneurysms due to degenerative disease
Q49113850	Aortic valve-sparing in 37 patients with Marfan syndrome: midterm results with David operation.
Q83531652	Aortic valve-sparing operation after correction of heart displacement due to pectus excavatum using Nuss procedure in a Marfan syndrome patient
Q79674483	Aortic valve-sparing operation in Marfan syndrome: what do we know after a decade?
Q82480729	Aortic wall mechanics in the Marfan syndrome assessed by transesophageal tissue Doppler echocardiography
Q57991077	Aortic wall shear stress in Marfan syndrome
Q38219936	Aortopathy in Marfan syndrome: an update.
Q39001215	Aortopathy in a Mouse Model of Marfan Syndrome Is Not Mediated by Altered Transforming Growth Factor β Signaling
Q51758994	Apical pulmonary lesions due to Marfan syndrome misdiagnosed as pulmonary tuberculosis.
Q37076634	Application of CRT-D in a Marfan syndrome patient with chronic heart failure accompanied by ventricular tachycardia and ventricular fibrillation
Q80603313	Application of dHPLC for mutation detection of the fibrillin-1 gene for the diagnosis of Marfan syndrome in a National Health Service Laboratory
Q92102212	Application of next-generation sequencing to screen for pathogenic mutations in 123 unrelated Chinese patients with Marfan syndrome or a related disease
Q43775802	Are Marfan syndrome and marfanoid patients distinguishable on long-term follow-up?
Q52992231	Areal bone mineral density in children and adolescents with Marfan syndrome: evidence of an evolving problem.
Q43933427	Arterial aneurysms: autosomal dominant polycystic kidney disease, Marfan syndrome or both?
Q82439115	Artisan aphakic intraocular lens implantation in cases of subluxated crystalline lenses due to Marfan syndrome
Q41570487	Ascending aortic aneurysm with or without features of Marfan syndrome and other fibrillinopathies: new insights
Q33672810	Ascertainment and severity of Marfan syndrome in a Scottish population
Q58114868	Assessment of Dural Ectasia Using Computed Tomodensitometry as a Criterion in Marfan Syndrome
Q51368544	Assessment of aortic root dimensions in patients with suspected Marfan syndrome: intraindividual comparison of contrast-enhanced and non-contrast magnetic resonance angiography with echocardiography.
Q45997458	Assessment of aortic stiffness in marfan syndrome using two-dimensional and Doppler echocardiography.
Q82825519	Assessment of carotid compliance using real time vascular ultrasound image analysis in Marfan syndrome
Q67519398	Assessment of ventricular performance after chronic beta-adrenergic blockade in the Marfan syndrome
Q92976921	Association between Marfan syndrome and oral health status: A systematic review and meta-analysis
Q42650213	Association between malignancies and Marfan syndrome: a population-based, nested case-control study in Taiwan
Q92531076	Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysis
Q57841911	Association of Marfan syndrome and bicuspid aortic valve: Frequency and outcome
Q90826120	Association of modifiers and other genetic factors explain Marfan syndrome clinical variability
Q91279959	Association of thoracic spine deformity and cardiovascular disease in a mouse model for Marfan syndrome
Q41907644	Atypical Neonatal Marfan Syndrome with p.Glu1073Lys Mutation of FBN1: the First Case in Korea
Q36316122	Augmentation index assessed by applanation tonometry is elevated in Marfan Syndrome
Q88750510	Authors' reply re: Peripartum type B aortic dissection in patients with Marfan syndrome who underwent aortic root replacement: a case series study
Q83464834	Autologous conjunctival epithelium transplantation and scleral patch graft for postlensectomy wound leakage in Marfan syndrome
Q93371473	Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variant
Q83207674	Badly engineered fibrillin lessons from molecular studies of marfan syndrome
Q70919575	Basic Defects in the Marfan Syndrome
Q45883374	Bentall Operation in a Patient With Severe Hemophilia A and Marfan Syndrome by Use of a Biologic Composite Graft
Q41577596	Bentall operation for a child with Marfan syndrome: a case report
Q52531842	Bentall operation, total aortic replacement and mitral valve replacement for a young adult with Marfan syndrome: a case of three-staged operation.
Q42170597	Beta-blocking therapy in patients with the Marfan syndrome and entire aortic replacement
Q92174486	Bicuspid Aortic Valve in Marfan Syndrome
Q89103628	Bilateral Crystalline Lens Subluxation in a Child With Marfan Syndrome
Q90932997	Bilateral Extracranial Internal Carotid Artery Aneurysms in a Patient with Marfan Syndrome: Case Report and Review of the Literature
Q58599257	Bilateral Immediate Sequential Vitrectomy and Lensectomy for Bilateral Lens Dislocation in Severe Neonatal Marfan Syndrome
Q72078511	Bilateral Renal Vein Thrombosis and Nephrotic Syndrome in a Patient with the Marfan Syndrome
Q91086055	Bilateral clear lens extraction and intraocular lens implantation in a child with microspherophakia and Marfan syndrome
Q99708730	Bilateral ectopia lentis in opposite quadrants in a child with Marfan syndrome
Q58806229	Bilateral lens coloboma associated with Marfan syndrome
Q90281250	Bilateral lens subluxation in Marfan syndrome
Q46463523	Bilateral pneumothorax and rupture of dissecting aortic aneurysm following a mitral valve replacement in Marfan syndrome: a case report
Q38095939	Bilateral radial artery aneurysms in the anatomical snuff box seen in marfan syndrome patient: case report and literature review
Q69105006	Biliary tract manifestations of the Marfan syndrome
Q90223128	Bimanual irrigation-aspiration for ectopia lentis and use of a small incision for 4-point scleral-sutured foldable intraocular lens and anterior vitrectomy in patients with Marfan syndrome
Q92963463	Biomarkers of Aortopathy in Marfan Syndrome
Q38930732	Biometry Characteristics in Adults and Children With Marfan Syndrome: From the Marfan Eye Consortium of Chicago
Q46195277	Biophysical properties of the aorta in patients with Marfan syndrome and related connective tissue disorders: evaluation with MRI and computational fluid dynamics modeling
Q52930904	Biophysical properties of the normal-sized aorta in patients with Marfan syndrome: evaluation with MR flow mapping.
Q88302773	Birth characteristics of women with Marfan syndrome, obstetric and neonatal outcomes of their pregnancies-A nationwide cohort and case-control study
Q50671398	Biventricular performance in patients with marfan syndrome without significant valvular disease: comparison to normal subjects and longitudinal follow-up.
Q91668322	Body Image in Patients with Marfan Syndrome
Q97685345	Bone Geometry, Density, and Microarchitecture in the Distal Radius and Tibia in Adults With Marfan Syndrome Assessed HR-pQCT
Q38121892	Bone lessons from Marfan syndrome and related disorders: fibrillin, TGF-B and BMP at the balance of too long and too short
Q73707970	Bone mineral density in Marfan syndrome
Q73731508	Bone mineral density in adults with Marfan syndrome
Q73420562	Bone mineral density in sixty adult patients with Marfan syndrome
Q46388841	Bovine model of Marfan syndrome results from an amino acid change (c.3598G > A, p.E1200K) in a calcium-binding epidermal growth factor-like domain of fibrillin-1.
Q68019048	Bronchial hyperreactivity in children with Marfan syndrome
Q91276786	Bypass and embolization for a vertebral artery aneurysm in a patient with Marfan syndrome
Q35124186	C596G mutation in FBN1 causes Marfan syndrome with exotropia in a Chinese family
Q77152805	CARDIAC CONDUCTION IN THE MARFAN SYNDROME
Q76963025	CASE OF MARFAN SYNDROME ASSOCIATED WITH SOME DERMATOLOGICAL DISORDERS
Q78293822	CHRONIC ATRIAL FLUTTER IN BROTHERS WITH THE MARFAN SYNDROME
Q77086195	CINE-AORTOGRAPHIC EVALUATION OF AORTIC INSUFFICIENCY. UNSUSPECTED IDIOPATHIC ANEURYSMAL DILATATION OF THE AORTIC ROOT AS A POSSIBLE INDICATION OF THE MARFAN SYNDROME
Q76660478	COARCTATION IN THE MARFAN SYNDROME
Q86494268	CORRIGENDUM: A clinical appraisal of different Z-score equations for aortic root assessment in the diagnostic evaluation of Marfan syndrome
Q72050405	Calcified annulus fibrosus with mitral insufficiency in the Marfan syndrome
Q72392434	Calcified annulus fibrosus with mitral insufficiency in the Marfan syndrome: with prosthetic replacement of the mitral valve
Q52815154	Capsular bag stabilization during lens extraction and intraocular lens implantation in cases of Marfan syndrome with ectopia lentis using ultra-high-viscosity ophthalmic viscosurgical devices.
Q69492213	Cardiac Manifestations of Marfan Syndrome in Infancy and Childhood
Q36563972	Cardiac remodeling in the mouse model of Marfan syndrome develops into two distinctive phenotypes
Q84264371	Cardiac tamponade due to perforation by an Amplatzer atrial septal occluder in a patient with Marfan syndrome
Q81387340	Cardiac transplantation in neonatal Marfan syndrome -- a life-saving approach
Q95417462	CardioPulse: options for pre-emptive aortic root surgery for people with Marfan syndrome
Q42373726	Cardiovascular Benefits of Moderate Exercise Training in Marfan Syndrome: Insights From an Animal Model.
Q91978388	Cardiovascular Magnetic Resonance Provides Evidence of Abnormal Myocardial Strain and Primary Cardiomyopathy in Marfan syndrome
Q92218873	Cardiovascular Management of Adults with Marfan Syndrome
Q57626246	Cardiovascular Management of Marfan Syndrome: Implications for Nurse Practitioners
Q92077172	Cardiovascular Operations in Children With Marfan Syndrome
Q68187485	Cardiovascular abnormalities in Marfan syndrome
Q34104219	Cardiovascular characteristics in Marfan syndrome and their relation to the genotype.
Q72359757	Cardiovascular lesions in bovine Marfan syndrome
Q30454633	Cardiovascular magnetic resonance in Marfan syndrome
Q80183360	Cardiovascular management of marfan syndrome in the young
Q77692360	Cardiovascular manifestations in Marfan syndrome
Q38215407	Cardiovascular manifestations in Marfan syndrome and related diseases; multiple genes causing similar phenotypes
Q68822267	Cardiovascular manifestations of Marfan syndrome. Apropos of 15 cases
Q83285248	Cardiovascular problems in pregnant women with marfan syndrome
Q80203472	Cardiovascular reoperations in Marfan syndrome
Q34204291	Cardiovascular surgery in Marfan syndrome: implications of new molecular concepts in thoracic aortic disease.
Q37493205	Cardiovascular surgery in children with Marfan syndrome or Loeys-Dietz syndrome
Q70054335	Carpal ligamentous laxity with bilateral perilunate dislocation in Marfan syndrome
Q74191279	Case 47: dural ectasia associated with Marfan syndrome
Q30459272	Case conference 6--1989. An 11-year-old boy with a diagnosis of the Marfan syndrome is admitted for emergency surgery after a 2-hour history of sharp, substernal chest pain
Q78799457	Case presentation: Marfan syndrome, dissecting aneurysm, intermittent occlusion of both coronary arteries
Q91645246	Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome
Q95841108	Causal Attributions in an Australian Aboriginal Family With Marfan Syndrome: A Qualitative Study
Q64043500	Causes of Mortality in the Marfan Syndrome(from a Nationwide Register Study)
Q66961596	Cell-free synthesis of hyaluronic acid in Marfan syndrome
Q57889810	Cellular and molecular studies of Marfan syndrome mutations identify co-operative protein folding in the cbEGF12–13 region of fibrillin-1
Q84966047	Central nervous system abnormalities in two cases with neonatal Marfan syndrome with novel mutations in the fibrillin‐1 gene
Q77782592	Central pulse pressure is a major determinant of ascending aorta dilation in Marfan syndrome
Q54046384	Cerebrotendinous xanthomatosis and Marfan syndrome - A picturesque combination.
Q100446746	Challenges and experiences in correcting scoliosis of a patient with Marfan Syndrome: A case report
Q74808983	Changes in aortic distensibility and pulse wave velocity assessed with magnetic resonance imaging following beta-blocker therapy in the Marfan syndrome
Q77799128	Changes of elastic fibers in musculoskeletal tissues of Marfan syndrome: a possible mechanism of joint laxity and skeletal overgrowth
Q53513524	Characteristic phenotype of immortalized periodontal cells isolated from a Marfan syndrome type I patient.
Q34606431	Characteristics in phenotypic manifestations of genetically proved Marfan syndrome in a Japanese population
Q34039474	Characteristics of children and young adults with Marfan syndrome and aortic root dilation in a randomized trial comparing atenolol and losartan therapy
Q73422108	Characterization of microsatellite markers flanking FBN1: utility in the diagnostic evaluation for Marfan syndrome
Q40674509	Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient.
Q88796540	Characterization of pain, disability, and psychological burden in Marfan syndrome
Q36990068	Characterization of the inflammatory cells in ascending thoracic aortic aneurysms in patients with Marfan syndrome, familial thoracic aortic aneurysms, and sporadic aneurysms
Q54271549	Chest wall reconstruction in Marfan syndrome following aortic root replacement.
Q57199761	Chiari-like tonsillar herniation associated with intracranial hypotension in Marfan syndrome
Q47686173	Childhood glaucoma in neonatal Marfan syndrome resulting from a novel FBN1 deletion
Q89249737	Chimney and sandwich stent grafts for hybrid repair of type A dissection late after a Bentall for Marfan syndrome
Q88076503	Chimneys and sandwiches for endovascular arch repair in patients with Marfan syndrome: Are we snorkeling in cloudy waters?
Q38698958	Chronic Debakey I aortic dissection in Marfan syndrome and hypertensive patients with modified stented elephant trunk surgery: a post-operative CT assessment
Q70795910	Chronic pulmonary tuberculosis in Marfan syndrome
Q39033457	Chronobiology of Acute Aortic Dissection in the Marfan Syndrome (from the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions and the International Registry of Acute Aortic Dissection).
Q93067648	Chylous Ascites Developing after Open Thoracoabdominal Aortic Aneurysm Repair in a Patient with Marfan Syndrome
Q33650710	Cine-CMR partial voxel segmentation demonstrates increased aortic stiffness among patients with Marfan syndrome
Q73434221	Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype-phenotype correlations in FBN1 exons 24-40
Q95530669	Classical Cardiovascular Manifestations of Marfan Syndrome
Q38421397	Classical and neonatal Marfan syndrome mutations in fibrillin-1 cause differential protease susceptibilities and protein function.
Q90191778	Classifying Ectopia Lentis in Marfan Syndrome into Five Grades of Increasing Severity
Q37399234	Clinical Characteristics of Marfan Syndrome in Korea
Q92174492	Clinical Significance of Aortic Root Modification Associated With Bicuspid Aortic Valve in Marfan Syndrome
Q38491523	Clinical and genetic analysis of Korean patients with Marfan syndrome: possible ethnic differences in clinical manifestation.
Q44919578	Clinical and genetic associations in Marfan syndrome and related disorders
Q68160899	Clinical and genetic heterogeneity of the Marfan syndrome
Q70948913	Clinical and immunohistochemical findings in a case of neonatal Marfan syndrome
Q44872505	Clinical and molecular exploration of the impact of radiation therapy on Marfan syndrome patients
Q43625160	Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations
Q78378892	Clinical considerations in the chiropractic management of the patient with Marfan syndrome
Q41692146	Clinical outcome in the Marfan syndrome with ascending aortic dilatation followed annually by echocardiography
Q83988429	Clinical presentation and echocardiographic findings of Thai patients with Marfan syndrome
Q81103795	Clinical presentation and surgical treatment of scoliosis in Marfan syndrome
Q91929056	Clinical significance of family history and bicuspid aortic valve in children and young adult patients with Marfan syndrome
Q43602632	Clinical signs of Marfan syndrome in children under 10 years of age
Q41734139	Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1]
Q66984509	Clinical variability in the Marfan syndrome(s)
Q56335487	Closure of a giant anterior sacral meningocele with an omental flap in a patient with Marfan syndrome: case report
Q67482103	Clustering of fibrillin (FBN1) missense mutations in Marfan syndrome patients at cysteine residues in EGF-like domains
Q99619277	Co-existence of Marfan syndrome and systemic sclerosis: A case report and a hypothesis suggesting a common link
Q47697831	Co-existence of mutations in the FBN1 gene and the ABCC6 gene in a patient with Marfan syndrome associated with pseudoxanthoma elasticum
Q34329711	Co-expression of FBN1 with mesenchyme-specific genes in mouse cell lines: implications for phenotypic variability in Marfan syndrome
Q40434563	Co-occurrence of Marfan syndrome and bipolar disorder: A fifteen year follow up.
Q51354108	Co-occurrence of Marfan syndrome and schizophrenia: what can be learned?
Q44810673	Co-occurrence of autosomal dominant polycystic kidney disease and Marfan syndrome in a kindred
Q81436354	Coexistence of anomalous origin of the coronary arteries and severe aortic regurgitation in Marfan syndrome
Q74216014	Coil embolization of a gluteal false aneurysm in a patient with Marfan syndrome
Q58769767	Coil embolization of bilateral internal mammary artery aneurysms is durable in a patient with Marfan syndrome
Q91176800	Coincidence of Andersen-Tawil syndrome and Marfan syndrome: A case report
Q71517546	Collagen metabolism in the fibroblasts derived from the skin of a 16-year-old patient with Marfan syndrome: a decreased rate of intracellular degradation of collagen
Q68339236	Color flow doppler assessment of aortic regurgitation complicated by aneurysmal dilation and dissection of the ascending aorta in the Marfan syndrome
Q79517251	Combined surgery for the treatment of bilateral subclavian artery aneurysm in Marfan syndrome
Q81260501	Comment on pregnancy and aortic root growth in the Marfan syndrome
Q102060282	Commentary: Danger of fluoroquinolones in Marfan syndrome
Q103834785	Commentary: The unacceptable aortic risk with fluoroquinolone exposure in Marfan syndrome
Q31155041	Comparative data on SD-OCT for the retinal nerve fiber layer and retinal macular thickness in a large cohort with Marfan syndrome
Q95645277	Comparison of Evolution of Aortic Root Dilation and Ghent Criteria in Preadolescents and Adolescents with and without Marfan Syndrome
Q53478171	Comparison of Long-Term Risk of Thoracic Aortic Aneurysm and Dissection in Patients With Bicuspid Aortic Valve and Marfan Syndrome After Aortic Valve Replacement.
Q73074678	Comparison of aortic elasticity in patients with the marfan syndrome with and without aortic root replacement
Q90347276	Comparison of biomechanical properties in ascending aortic aneurysms of patients with congenital bicuspid aortic valve and Marfan syndrome
Q57224318	Comparison of cardiovascular and skeletal features of primary mitral valve prolapse and Marfan syndrome
Q37382054	Comparison of clinical characteristics and frequency of adverse outcomes in patients with Marfan syndrome diagnosed in adulthood versus childhood
Q51027497	Comparison of clinical outcomes between iris-fixated anterior chamber intraocular lenses and scleral-fixated posterior chamber intraocular lenses in Marfan syndrome with lens subluxation.
Q54705122	Comparison of clinical presentations and outcomes between patients with TGFBR2 and FBN1 mutations in Marfan syndrome and related disorders.
Q78727483	Comparison of outcome of the Marfan Syndrome in patients diagnosed at age < or =6 years versus those diagnosed at >6 years of age
Q35814868	Comparison of posterior correction results between Marfan syndrome scoliosis and adolescent idiopathic scoliosis-a retrospective case-series study.
Q47589920	Comparison of the Effect of Aliskiren Versus Negative Controls on Aortic Stiffness in Patients With Marfan Syndrome Under Treatment With Atenolol
Q53436926	Comparison of the background, needs, and expectations for genetic counseling of adults with experience with Down syndrome, Marfan syndrome, and neurofibromatosis.
Q92722491	Compound heterozygous mutations in FBN1 in a large family with Marfan syndrome
Q82852504	Compound-heterozygous Marfan syndrome
Q62977736	Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypes
Q59741483	Computed tomography coronary angiography should be performed in all patients with Marfan Syndrome prior to aortic root replacement
Q91097378	Concomitant aortic root and pectus deformity repair in Marfan syndrome patients
Q84571669	Concomitant mitral valve replacement and re-re-repair of severe pectus deformity correction in a patient with Marfan syndrome
Q38057988	Concomitant occurrence of hypohyperdontia in a patient with Marfan syndrome: a review of the literature and report of a case
Q67387573	Congenital Marfan syndrome
Q49121017	Congenital Marfan syndrome with contractures. A clinicopathological report
Q70691611	Congenital contractural arachnodactyly, keratoconus, and probable Marfan syndrome in the same pedigree
Q69620118	Congenital contractural arachnodactyly. A heritable disorder of connective tissue distinct from Marfan syndrome
Q35571911	Congenital diaphragmatic eventration and bilateral uretero-hydronephrosis in a patient with neonatal Marfan syndrome caused by a mutation in exon 25 of the FBN1 gene and review of the literature
Q60693056	Congenital lumbar spinal stenosis associated with Marfan syndrome
Q77314590	Congenital obstructive azoospermia in a man with Marfan syndrome
Q104466926	Connective tissue nevus in Marfan syndrome successfully treated with intralesional steroid injections
Q87967060	Consecutive operative procedures in patients with Marfan syndrome up to 28 years after initial aortic root surgery
Q92098772	Consecutive surgical sequelae in children and adolescents with Marfan syndrome after primary cardiovascular surgical interventions
Q89681162	Consultation Section: Glaucoma. Cataract, glaucoma, possible Marfan syndrome, and conception aspirations
Q53219724	Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands.
Q55015647	Corneal Curvature, Astigmatism, and Aberrations in Marfan Syndrome with Lens Subluxation: Evaluation by Pentacam HR System.
Q36403212	Corneal Deformation Response and Ocular Geometry: A Noninvasive Diagnostic Strategy in Marfan Syndrome
Q84500387	Corneal curvature, pachymetry, and endothelial cell density in Marfan syndrome
Q73084212	Corneal wrinkling in a hydrogel contact lens wearer with Marfan syndrome
Q87981123	Coronary Involvement in Marfan Syndrome: The Role of Electrocardiographically Gated Computed Tomography Angiography
Q74625068	Coronary artery aneurysm in a patient with Marfan syndrome
Q92043345	Correction of Scoliosis with Large Thoracic Curves in Marfan Syndrome: Does the High-Density Pedicle Screw Construct Contribute to Better Surgical Outcomes
Q91237939	Correction of the Marfan Syndrome Pathogenic FBN1 Mutation by Base Editing in Human Cells and Heterozygous Embryos
Q58197667	Correlation of a recurrent FBN1 mutation (R122C) with an atypical familial Marfan syndrome phenotype
Q87807806	Correspondence letter by Mkrtchyan and Fratz regarding article "aortic biomechanics by magnetic resonance: early markers of aortic disease in Marfan syndrome regardless of aortic dilatation?"
Q86910077	Correspondence regarding: Distinct effects of losartan and atenolol on vascular stiffness in Marfan syndrome by Bhatt et al
Q73074673	Cosegregation of the Marfan syndrome and the long QT syndrome in the same family leads to a severe cardiac phenotype
Q91908208	Craniofacial characterization of Marfan Syndrome
Q53934823	Craniofacial manifestations in the Marfan syndrome: palatal dimensions and a comparative cephalometric analysis.
Q80954083	Craniofacial structure in Marfan syndrome: a cephalometric study
Q56383808	Craniosynostosis with Marfan syndrome, hand and foot anomalies
Q41040310	Current diagnosis and prescription for Marfan syndrome: when to operate
Q72427396	Current diagnosis and prescription for the Marfan syndrome: aortic root and valve replacement
Q36766898	Current role of endovascular therapy in Marfan patients with previous aortic surgery
Q73627270	Current status of thoracoabdominal aortic aneurysm repair in Marfan syndrome
Q92634017	Cyclophilin A/EMMPRIN Axis Is Involved in Pro-Fibrotic Processes Associated with Thoracic Aortic Aneurysm of Marfan Syndrome Patients
Q90995298	Cyst Masquerading as Inadvertent Bleb After a Scleral-Fixated Intraocular Lens in Marfan Syndrome: A Case Report
Q86525360	Cystic medial necrosis and internal carotid artery dissection in a marfan sibling: Partial expression of marfan syndrome
Q41051334	DNA diagnostics of the Marfan syndrome: application of amplifiable polymorphic markers
Q90633464	DNA methylation ambiguity in the Fibrillin-1 (FBN1) CpG island shore possibly involved in Marfan syndrome
Q41586331	DPY-17 and MUA-3 Interact for Connective Tissue-Like Tissue Integrity in Caenorhabditis elegans: A Model for Marfan Syndrome
Q89585356	Decision-making at initial surgery for type A aortic dissection in patients with Marfan syndrome: proximal or extensive repair
Q41457834	Decision-making in aortic root surgery in Marfan syndrome: bleeding, thromboembolism and risk of reintervention after valve-sparing or mechanical aortic root replacement
Q48228144	Decrease in pulmonary artery pressure after administration of thoracic epidural anesthesia in a patient with Marfan syndrome awaiting aortic valve replacement procedure
Q88540405	Decreased Aortic Elasticity in Children With Marfan Syndrome or Loeys-Dietz Syndrome
Q83194475	Decreased aortic root distensibility rather than increased aortic root diameter as an important cardiovascular risk factor in the Marfan syndrome
Q70550012	Decreased extracellular deposition of fibrillin and decorin in neonatal Marfan syndrome fibroblasts
Q39043057	Decreased frequency of FBN1 missense variants in Ghent criteria-positive Marfan syndrome and characterization of novel FBN1 variants
Q90676560	Decreased rotational flow and circumferential wall shear stress as early markers of descending aorta dilation in Marfan syndrome: a 4D flow CMR study
Q40662043	Defective secretion of recombinant fragments of fibrillin-1: implications of protein misfolding for the pathogenesis of Marfan syndrome and related disorders
Q33594765	Deficiencies of fibrillin and decorin in fibroblast cultures of a patient with neonatal Marfan syndrome
Q92583328	Deficiency of Circulating Monocytes Ameliorates the Progression of Myxomatous Valve Degeneration in Marfan Syndrome
Q28253949	Deficient expression of the gene coding for decorin in a lethal form of Marfan syndrome
Q89349198	Definition and delivery of an aortopathy bundle of care (ABC): a tool for improving diagnosis and management of Marfan syndrome and related conditions
Q69407683	Delusions in Marfan syndrome
Q78178619	Denaturing HPLC-identified novel FBN1 mutations, polymorphisms, and sequence variants in Marfan syndrome and related connective tissue disorders
Q55383374	Dental findings in marfan syndrome: a case report.
Q35628022	Design and rationale of a prospective, collaborative meta-analysis of all randomized controlled trials of angiotensin receptor antagonists in Marfan syndrome, based on individual patient data: A report from the Marfan Treatment Trialists' Collaborat
Q50000274	Detection and a functional characterization of the novel FBN1 intronic mutation underlying Marfan syndrome: case presentation.
Q83220763	Detection of 53 FBN1 mutations (41 novel and 12 recurrent) and genotype-phenotype correlations in 113 unrelated probands referred with Marfan syndrome, or a related fibrillinopathy
Q30535299	Detection of abnormal aortic elastic properties in asymptomatic patients with Marfan syndrome by combined transoesophageal echocardiography and acoustic quantification
Q74429237	Detection of six novel FBN1 mutations in British patients affected by Marfan syndrome
Q91676041	Detection of ten novel FBN1 mutations in Chinese patients with typical or incomplete Marfan syndrome and an overview of the genotype-phenotype correlations
Q44706171	Detection of thirty novel FBN1 mutations in patients with Marfan syndrome or a related fibrillinopathy
Q41062566	Determination of the molecular basis of Marfan syndrome: a growth industry
Q57197781	Determination of the molecular basis of Marfan syndrome: a growth industry
Q90336966	Developmental abnormalities in the cornea of a mouse model for Marfan syndrome
Q74579734	Diagnosing Marfan syndrome is still based on clinical characteristics
Q38207922	Diagnosis and treatment of Marfan syndrome: an update
Q35575539	Diagnosis of Marfan syndrome by computed tomography
Q82330061	Diagnostic challenges of Marfan syndrome in an XYY young man
Q33213910	Diagnostic power of aortic elastic properties in young patients with Marfan syndrome
Q62607051	Diastolic subclinical primary alterations in marfan syndrome and marfan-related disorders
Q92994244	Differences in Cardiovascular Manifestation of Marfan Syndrome Between Children and Adults
Q47117228	Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome
Q33258356	Different patterns of aortic wall elasticity in patients with Marfan syndrome: a noninvasive follow-up study
Q104463225	Differential diagnosis of Marfan syndrome based on ocular biologic parameters
Q34341127	Differential effects of alendronate and losartan therapy on osteopenia and aortic aneurysm in mice with severe Marfan syndrome
Q94368156	Differential effects of alendronate and losartan therapy on osteopenia and aortic aneurysm in mice with severe Marfan syndrome
Q38391989	Difficulties in diagnosing Marfan syndrome using current FBN1 databases
Q58592624	Diffuse Myocardial Fibrosis in Children and Adolescents With Marfan Syndrome and Loeys-Dietz Syndrome
Q72812026	Dilatation of the aorta and pulmonary artery with aortic and pulmonary insufficiency in the presence of a ventricular septal defect and infundibular pulmonic stenosis. Report of a case of forme fruste of the Marfan syndrome
Q79274741	Dilatation of the aortic sinuses in the Marfan syndrome: roentgen findings in five new cases
Q42821154	Dilatation of the great arteries in an infant with marfan syndrome and ventricular septal defect
Q82789575	Dilated cardiomyopathy in a patient with Marfan syndrome accompanied by chronic type A aortic dissection and right atrial thrombus
Q46499485	Dilation of peripheral vessels in Marfan syndrome: importance of thoracoabdominal MR angiography.
Q35224497	Dimorphic effects of transforming growth factor-β signaling during aortic aneurysm progression in mice suggest a combinatorial therapy for Marfan syndrome
Q35778595	Disease-specific Growth Charts of Marfan Syndrome Patients in Korea
Q46123260	Disease-specific growth charts of Marfan syndrome in Korea
Q83403099	Dissecting aortic aneurysm with Marfan syndrome
Q72468288	Dissecting aortic aneurysms that occurred in aged brothers without Marfan syndrome
Q43575327	Dissecting basilar artery aneurysm in Marfan syndrome: case report
Q82835511	Dissection in Marfan syndrome: the importance of the descending aorta
Q86584171	Distal aorta: the next frontier in managing Marfan syndrome aortic disease
Q82766124	Distal aortic and peripheral arterial aneurysms in patients with Marfan syndrome
Q33640012	Distinct defects in collagen microarchitecture underlie vessel-wall failure in advanced abdominal aneurysms and aneurysms in Marfan syndrome
Q92319087	Divergent effects of canonical and non-canonical TGF-β signalling on mixed contractile-synthetic smooth muscle cell phenotype in human Marfan syndrome aortic root aneurysms
Q36986441	Diverticulitis complicated by fistulous communication of sigmoid colon with anterior sacral meningocele in a patient with Marfan syndrome
Q37462387	Does altered aortic flow in marfan syndrome relate to aortic root dilatation?
Q72273382	Dolichonychia in a patient with the Marfan syndrome
Q79990472	Dolichonychia in women with Marfan syndrome
Q92054641	Double decentred lenses in an eye: a therapeutic dilemma in Marfan syndrome
Q33677788	Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndrome
Q39654561	Down syndrome masked by Marfan syndrome in a neonate
Q99616344	Down syndrome with co-occurring Marfan syndrome
Q83276641	Drug shows promise for marfan syndrome
Q34051477	Drug‐Based Therapies for Vascular Disease in Marfan Syndrome: From Mouse Models to Human Patients
Q70013027	Ductus arteriosus aneurysm in Marfan syndrome
Q49125382	Dural ectasia and FBN1 mutation screening of 40 patients with Marfan syndrome and related disorders: role of dural ectasia for the diagnosis.
Q104746763	Dural ectasia and intracranial hypotension in Marfan syndrome
Q57641015	Dural ectasia as an incidental finding on MRI in a patient with Marfan syndrome
Q28280819	Dural ectasia as presenting symptom of Marfan syndrome
Q79659944	Dural ectasia in Marfan syndrome
Q85055677	Dural ectasia in Marfan syndrome
Q93178898	Dural ectasia in Marfan syndrome and other hereditary connective tissue disorders: a 10-year follow-up study
Q45808431	Dural ectasia in Marfan syndrome: a case control study
Q82759208	Dural ectasia in children with Marfan syndrome: a prospective, multicenter, patient-control study
Q73634804	Dural ectasia in the Marfan syndrome: MR and CT findings and criteria
Q73888788	Dural ectasia is associated with back pain in Marfan syndrome
Q29618845	Dysregulation of TGF-beta activation contributes to pathogenesis in Marfan syndrome
Q38440177	Early and 1-year outcomes of aortic root surgery in patients with Marfan syndrome: a prospective, multicenter, comparative study
Q84594998	Early and late results of graft replacement for dissecting aneurysm of thoracoabdominal aorta in patients with Marfan syndrome
Q73195617	Early and long-term results of a valve-sparing operation for Marfan syndrome
Q87378119	Early detection of cardiac dysfunction by strain and strain rate imaging in children and young adults with marfan syndrome
Q80763839	Early impairment of left ventricular long-axis systolic function demonstrated by reduced atrioventricular plane displacement in patients with Marfan syndrome
Q78961375	Early manifestations of the cardiovascular disorders in Marfan syndrome
Q36623502	Early onset marfan syndrome: Atypical clinical presentation of two cases
Q91808180	Early-Onset Marfan Syndrome: A Case Series
Q81410568	Echocardiographic Doppler assessment of the biophysical properties of the aorta in pediatric patients with the Marfan syndrome
Q72320869	Echocardiographic diagnosis of fetal Marfan syndrome at 34 weeks' gestation
Q81154099	Echocardiometric evaluation of cardiovascular abnormalities in Marfan syndrome
Q30393311	Economic and care considerations of Marfan syndrome
Q57200289	Ectopia Lentis with Microspherophakia in Marfan Syndrome Resolved with Mydriasis
Q84965849	Ectopia lentis as the presenting and primary feature in Marfan syndrome
Q30454065	Edgar Allan Poe: a case description of the Marfan syndrome in an obscure short story
Q42648434	Editorial Commentary: Understanding Marfan syndrome, or "how not to invent the light bulb".
Q82800171	Editorial comment: New diagnostic criteria for Marfan syndrome
Q84464868	Effect of a physical exercise program in a patient with Marfan syndrome and ventricular dysfunction
Q36506118	Effect of angiotensin II receptor blocker on experimental periodontitis in a mouse model of Marfan syndrome
Q82947353	Effect of aortic stiffness on left ventricular long-axis systolic function in adults with Marfan syndrome
Q72690059	Effect of beta-adrenergic blockade on aortic root rate of dilation in the Marfan syndrome
Q77808605	Effect of long-term beta-blockade on aortic root compliance in patients with Marfan syndrome
Q35946338	Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study
Q35209750	Effect of native aortic valve sparing aortic root reconstruction surgery on short- and long-term prognosis in Marfan syndrome patients:a meta-analysis
Q38394699	Effect of perindopril on large artery stiffness and aortic root diameter in patients with Marfan syndrome: a randomized controlled trial
Q53444109	Effect of personalized external aortic root support on aortic root motion and distension in Marfan syndrome patients.
Q54972636	Effect of the Antioxidant Lipoic Acid in Aortic Phenotype in a Marfan Syndrome Mouse Model.
Q83797813	Effects of atenolol, perindopril and verapamil on haemodynamic and vascular function in Marfan syndrome - a randomised, double-blind, crossover trial
Q100490816	Effects of fibrillin mutations on the behavior of heart muscle cells in Marfan syndrome
Q83229855	Efficacy of desmopressin in preventing hemorrhagic complications in a patient with Marfan syndrome undergoing cardiac surgery
Q49083618	Efficacy of losartan as add-on therapy to prevent aortic growth and ventricular dysfunction in patients with Marfan syndrome: a randomized, double-blind clinical trial.
Q60637215	Efficacy of losartan vs. atenolol for the prevention of aortic dilation in Marfan syndrome: a randomized clinical trial
Q28272021	Ehlers-Danlos syndromes and Marfan syndrome
Q93945608	Eight novel mutations of the FBN1 gene found in Japanese patients with Marfan syndrome
Q78165120	Elastic fibers of musculoskeletal tissues in bovine Marfan syndrome: a morphometric study
Q93572984	Elastin and collagen in the aortic wall: changes in the Marfan syndrome and annuloaortic ectasia
Q68707384	Elemental composition of human aorta in Marfan syndrome
Q74601981	Eleven cases of surgery for Marfan syndrome
Q38654233	Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 7: Aortic Diseases, Including Marfan Syndrome: A Scientific Statement From the American Heart Association and American College of
Q86637536	Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 7: Aortic Diseases, Including Marfan Syndrome: A Scientific Statement From the American Heart Association and American College of
Q90757018	Embolic stroke, left atrial myxoma and gigantism in a patient with Carney complex with additional features suggestive of Marfan syndrome
Q38134947	Emergency cesarean section due to acute aortic dissection type A (Debakey I) without Marfan syndrome: a case report and review of the literature
Q66953677	Endocarditis and the Marfan Syndrome
Q72997118	Endoluminal replacement of the entire aorta for acute type A aortic dissection in a patient with Marfan syndrome
Q42468226	Endothelial function in Marfan syndrome: selective impairment of flow-mediated vasodilation
Q41813012	Endovascular Repair of Aortic Dissection in Marfan Syndrome: Current Status and Future Perspectives
Q90874613	Endovascular Repair of Bilateral Internal Mammary Artery Aneurysms in a Patient with Marfan Syndrome
Q90777944	Endovascular Trapping of Large Cervical Carotid Pseudoaneurysm in Marfan Syndrome Presenting with Progressive Respiratory Distress
Q91508481	Endovascular abdominal aortic aneurysm repair in patients with Marfan syndrome
Q39970083	Endovascular aneurysm repair using a reverse chimney technique in a patient with Marfan syndrome and contained ruptured chronic type B dissection.
Q39771597	Endovascular repair of a symptomatic subclavian artery aneurysm in a patient with Marfan syndrome: a case report
Q47141585	Endovascular surgery in Marfan syndrome: CON.
Q47103401	Endovascular therapy in Marfan syndrome: PRO.
Q38070226	Endovascular treatment for type B dissection in Marfan syndrome: is it worthwhile?
Q42594627	Endovascular treatment of type B dissection in patients with Marfan syndrome: mid-term outcomes and aortic remodeling.
Q38568416	Engineered mutations in fibrillin-1 leading to Marfan syndrome act at the protein, cellular and organismal levels
Q96950706	Enhanced Notch3 signaling contributes to pulmonary emphysema in a Murine Model of Marfan syndrome
Q73939680	Enzymatic mutation detection (EMD) of novel mutations (R565X and R1523X) in the FBN1 gene of patients with Marfan syndrome using T4 endonuclease VII
Q34658683	Epidemiological profile of Marfan syndrome in a general population: a national database study
Q33762331	Epidural Anesthesia for Cesarean Section in a Pregnant Woman with Marfan Syndrome and Dural Ectasia.
Q34765778	Epidural anesthesia for cesarean section in a patient with Marfan syndrome and dural ectasia -A case report-.
Q94483038	Erratum to: Cataract, glaucoma, possible Marfan syndrome, and conception aspirations
Q77365444	Erratum: Detection of six novel FBN1 mutations in British patients affected by Marfan syndrome
Q68444362	Estrogen treatment of excessively tall girls with Marfan syndrome
Q47138067	Etiology and pathogenesis of the Marfan syndrome: current understanding
Q49048666	Evaluating Japanese patients with the Marfan syndrome using high-throughput microarray-based mutational analysis of fibrillin-1 gene.
Q77880366	Evaluation and application of denaturing HPLC for mutation detection in Marfan syndrome: Identification of 20 novel mutations and two novel polymorphisms in the FBN1 gene
Q95432342	Evaluation of the adolescent or adult with some features of Marfan syndrome
Q45123658	Evaluation of the aorta in the Marfan syndrome by magnetic resonance imaging
Q22065344	Evidence for a critical contribution of haploinsufficiency in the complex pathogenesis of Marfan syndrome
Q61480549	Evidence for oxidative stress in plasma of patients with Marfan syndrome
Q57213432	Evidence of aortic dissection and Marfan syndrome in a mummy from the Capuchin Catacombs of Palermo, Sicily
Q33674440	Exclusion of the alpha 2(I) and alpha 1(III) collagen genes as the mutant loci in a Marfan syndrome family.
Q88404972	Executive function and quality of life in individuals with Marfan syndrome
Q77468686	Exercise and the Marfan syndrome
Q37568804	Exome sequencing identified new mutations in a Marfan syndrome family
Q91271256	Expanding the spectrum of causative mutations of Marfan syndrome: Is there a role for the elastin gene?
Q39830013	Experimental and bioinformatic characterisation of the promoter region of the Marfan syndrome gene, FBN1.
Q34533265	Expression of FBN1 during adipogenesis: Relevance to the lipodystrophy phenotype in Marfan syndrome and related conditions
Q79839122	Expression of matrix metalloproteinases and endogenous inhibitors within ascending aortic aneurysms of patients with Marfan syndrome
Q78299225	Expression of peroxisome proliferator-activated receptor-gamma in vascular smooth muscle cells is upregulated in cystic medial degeneration of annuloaortic ectasia in Marfan syndrome
Q38697306	Extended aortic repair using frozen elephant trunk technique for Marfan syndrome with acute aortic dissection
Q77953376	Extensive aortic reconstruction for aortic aneurysms in Marfan syndrome
Q75184935	Extensive aortic surgery in Marfan syndrome: 16-year experience
Q84971214	External aortic root support for Marfan syndrome: early clinical results in the first 20 recipients with a bespoke implant
Q91236782	Extracranial Internal Carotid Artery Aneurysm in a Patient with Marfan Syndrome
Q58000668	Extradural Arachnoid Cyst With Lumbosacral Cord and Root Compression in Marfan Syndrome
Q73969599	FBN1 exon 2 splicing error in a patient with Marfan syndrome
Q92516865	FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies
Q47724847	FBN1 mutation in Chinese patients with Marfan syndrome and its gene diagnosis using haplotype linkage analysis.
Q34774069	FBN1 mutation screening of patients with Marfan syndrome and related disorders: detection of 46 novel FBN1 mutations.
Q38903109	FBN1: The disease-causing gene for Marfan syndrome and other genetic disorders
Q43073730	FBN2 mutation associated with manifestations of Marfan syndrome and congenital contractural arachnodactyly
Q38698527	Factors influencing prognosis in patients with marfan syndrome after aortic surgery
Q67930772	Familial Multiple Bilateral Pneumothorax Associated with Marfan Syndrome
Q53565277	Familial neonatal Marfan syndrome due to parental mosaicism of a missense mutation in the FBN1 gene.
Q82213322	Familial spontaneous pneumothorax in two adult siblings with Marfan syndrome
Q57222030	Family history of severe cardiovascular disease in Marfan syndrome is associated with increased aortic diameter and decreased survival
Q72761012	Family studies of the Marfan syndrome
Q59337327	Family-based whole-exome sequencing identifies novel loss-of-function mutations of for Marfan syndrome
Q33156499	Fatal aortic dissection in a patient with a family history of Marfan syndrome
Q36023024	Fatal case of brucellosis misdiagnosed in early stages of Brucella suis infection in a 46-year-old patient with Marfan syndrome
Q64118640	Fate of distal aorta after frozen elephant trunk and total arch replacement for type A aortic dissection in Marfan syndrome
Q87650602	Fatigue in adults with Marfan syndrome, occurrence and associations to pain and other factors
Q49168048	Fatigue, cognitive functioning and psychological distress in Marfan syndrome, a pilot study.
Q91914662	Features of Marfan syndrome not listed in the Ghent nosology - the dark side of the disease
Q42376279	Fell-Muir Lecture: Fibrillin microfibrils: structural tensometers of elastic tissues?
Q35631973	Femtosecond Laser-assisted Cataract Surgery in Patients With Marfan Syndrome and Subluxated Lens.
Q37589234	Femur Neck Fracture in a Young Marfan Syndrome Patient
Q82883804	Fenestrated endograft repair of suprarenal aortic patch aneurysm in a patient with Marfan syndrome
Q71121889	Fetal Marfan syndrome: prenatal ultrasound diagnosis with pathological confirmation of skeletal and aortic lesions
Q82254141	Fetuin-A serum levels in patients with aortic aneurysms of Marfan syndrome and atherosclerosis
Q67481793	Fibrillin (FBN1) mutations in Marfan syndrome
Q45093455	Fibrillin abnormalities and prognosis in Marfan syndrome and related disorders
Q58375267	Fibrillin domain folding and calcium binding: significance to Marfan syndrome
Q73558998	Fibrillin gene (FBN1) mutations in Japanese patients with Marfan syndrome
Q36629557	Fibrillin in Marfan syndrome and tight skin mice provides new insights into transforming growth factor-beta regulation and systemic sclerosis.
Q38807710	Fibrillin-1 mgΔ(lpn) Marfan syndrome mutation associates with preserved proteostasis and bypass of a protein disulfide isomerase-dependent quality checkpoint
Q28256705	Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies
Q57273788	Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies
Q41099958	Fibrillln mutations in Marfan syndrome and related phenotypes
Q28298628	Fibulin-2: genetic mapping and exclusion as a candidate gene in Marfan syndrome type 2
Q35643503	Fifteen novel FBN1 mutations causing Marfan syndrome detected by heteroduplex analysis of genomic amplicons
Q48697947	First non-complicated thrombolysis in a young patient with Marfan syndrome and brainstem ischaemic stroke.
Q54502663	First report of the genetic background of Marfan syndrome in Polish patients.
Q47911031	Florida Sleeve Procedure Is Durable and Improves Aortic Valve Function in Marfan Syndrome Patients
Q59261189	Fluid dynamics of aortic root dilation in Marfan syndrome
Q91644307	Fluid-structure interaction simulations outperform computational fluid dynamics in the description of thoracic aorta haemodynamics and in the differentiation of progressive dilation in Marfan syndrome patients
Q104608002	Forensic case of a pregnant woman with Marfan syndrome
Q78037959	Free information about Marfan syndrome available to school nurses
Q56988722	Frequency and Age-Related Course of Mitral Valve Dysfunction in the Marfan Syndrome
Q78039420	Frequency of coronary ostial aneurysms after aortic root surgery in patients with the Marfan syndrome
Q72813265	From fluorescence to the gene: the skin in the Marfan syndrome
Q57864618	Frozen elephant trunk for aortic arch dissection in patients with Marfan syndrome: Are we there yet?
Q92471106	Full Mouth Rehabilitation with Implant-Prosthesis in Marfan Syndrome Patient Clinical Report and Literature Review
Q81016921	Functional pulmonary atresia in a patient with neonatal Marfan syndrome caused by a c.3602G>A mutation in exon 29 of the FBN1 gene
Q92783676	Further Defining the Phenotypic Spectrum of B3GAT3 Mutations and Literature Review on Linkeropathy Syndromes
Q78402832	Fusiform aneurysm of the scalp: an unusual cause of focal headache in Marfan syndrome
Q91167966	Gastrointestinal Symptoms in Marfan Syndrome and Hypermobile Ehlers-Danlos Syndrome
Q92151736	Gelatinolytic activity in gingival crevicular fluid and saliva of growing patients with Marfan syndrome: a case-control study
Q45395349	Gender and psychiatric manifestations in Marfan syndrome - is there a link?
Q85352504	Gene polymorphisms as risk factors for predicting the cardiovascular manifestations in Marfan syndrome. Role of folic acid metabolism enzyme gene polymorphisms in Marfan syndrome
Q78950757	Gene symbol: FBN1. Disease: Marfan syndrome
Q66400087	Generation of Marfan Syndrome and Fontan Cardiovascular Models Using Patient-specific Induced Pluripotent Stem Cells
Q92359612	Generation of a human iPSC line from a patient with Marfan syndrome caused by mutation in FBN1
Q92416444	Generation of a human induced pluripotent stem cell line (NCCDFWi001-A) from a Marfan syndrome patient carrying two FBN1 variants (c.2613A > C and c.684_736 + 4del)
Q40739637	Genetic Counseling of Families with Marfan Syndrome and Other Disorders Showing a Marfanoid Body Habitus
Q91675779	Genetic analysis and preimplantation genetic diagnosis of Chinese Marfan syndrome patients
Q36526049	Genetic dissection of marfan syndrome and related connective tissue disorders: an update 2012.
Q45169553	Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5. The International Marfan Syndrome Collaborative Study
Q92997299	Genome Sequencing Identifies the Pathogenic Variant Missed by Prior Testing in an Infant with Marfan Syndrome
Q72676723	Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome
Q101565995	Genotype FBN1/Phenotype relationship in a cohort of patients with Marfan syndrome
Q35673403	Genotype-phenotype analysis of F-helix mutations at the kinase domain of TGFBR2, including a type 2 Marfan syndrome familial study.
Q35792708	Ghent Criteria an Aid to Diagnose Latent Systemic Diseases in Marfan Syndrome
Q91217270	Giant Aortic Root Aneurysm in a Patient with D-Transposition of the Great Arteries and Marfan Syndrome
Q101403859	Giant Ascending Aortic Aneurysm with Painless Dissection in a Patient with Marfan Syndrome
Q36725437	Giant Pulmonary Artery Aneurysm in a Patient With Marfan Syndrome and Pulmonary Hypertension.
Q82940811	Giant aortic root aneurysm in Marfan syndrome: a rare complication in early childhood
Q34163753	Glaucoma in the Marfan syndrome
Q81042154	Grand rounds. Chest pain in a woman with Marfan syndrome
Q88851101	Gross deletions in FBN1 results in variable phenotypes of Marfan syndrome
Q93664182	Growth and anthropometrics in the Marfan syndrome
Q78010930	Growth and maturation in Marfan syndrome
Q104606762	Growth-friendly Spinal Instrumentation in Marfan Syndrome Achieves Sustained Gains in Thoracic Height Amidst High Rates of Implant Failure
Q79451103	Guidelines for the diagnosis and management of Marfan syndrome
Q57068421	Health-Related Quality of Life in Children and Young Adults with Marfan Syndrome
Q103794276	Health-related quality of life in Marfan syndrome: a 10-year follow-up
Q49096977	Health-related quality of life in Marfan syndrome: a cross-sectional study of Short Form 36 in 84 adults with a verified diagnosis.
Q47911657	Health-related quality of life is unimpaired in children and adolescents with Marfan syndrome despite its distinctive phenotype
Q95924278	Heart Transplantation Outcomes in Patients with Marfan Syndrome: UNOS Registry Analysis
Q33165803	Heart rate turbulence and deceleration capacity for risk prediction of serious arrhythmic events in Marfan syndrome
Q81372793	Hemifacial spasm in a patient with Marfan syndrome and Chiari I malformation. Case report
Q73233070	Hemopneumothorax associated with Marfan syndrome and congenital afibrinogenemia
Q91318992	Hemostatic abnormalities in adult patients with Marfan syndrome
Q51334906	Heparin resistance and Marfan syndrome: is there any correlation?
Q58071857	Heterogeneous aortic response to acute β-adrenergic blockade in Marfan syndrome
Q34331334	Heterozygous TGFBR2 mutations in Marfan syndrome
Q99576541	Heterozygous nonsense variant of CHD8 in a patient with forme-fruste Marfan syndrome and intellectual disability
Q73906766	Hiatus/paraesophageal hernias in neonatal Marfan syndrome
Q44673836	High incidence and severity of periodontitis in patients with Marfan syndrome in Japan
Q29994788	High-Resolution Morphological Approach to Analyse Elastic Laminae Injuries of the Ascending Aorta in a Murine Model of Marfan Syndrome
Q66923957	Histidinemia with features of the Marfan syndrome
Q70861678	Histomorphometric parameters and susceptibility to neutrophil elastase degradation of skin elastic fibres from healthy individuals and patients with Marfan syndrome, Ehlers-Danlos type IV, and pseudoxanthoma elasticum
Q56688676	Histopathology and fibrillin-1 distribution in severe early onset Marfan syndrome
Q72830687	Histopathology of Striae Distensae, with Special Reference to Striae and Wound Healing in the Marfan Syndrome*
Q36849812	Histopathology of aortic complications in bicuspid aortic valve versus Marfan syndrome: relevance for therapy?
Q44652964	Homocysteine, Marfan syndrome and arteriosclerosis
Q72652601	Homocystinuria simulating the Marfan syndrome
Q85820596	Homozygosity for a FBN1 missense mutation causes a severe Marfan syndrome phenotype
Q86646285	How to treat Marfan syndrome: an update
Q86302473	Huge ascending aortic aneurysm in a 7-year-old patient with Marfan syndrome
Q38785372	Human embryonic stem cells derived from abnormal blastocyst donated by Marfan syndrome patient
Q53053622	Hybrid Endovascular Treatment of an Aortic Root and Thoracoabdominal Aneurysm in a High-Risk Patient With Marfan Syndrome
Q82995284	Hybrid endovascular repair of an aneurysmal chronic type B dissection in a patient with Marfan syndrome with an aberrant right subclavian artery
Q84290695	Hybrid repair of bilateral subclavian artery aneurysms in a patient with Marfan syndrome
Q89221745	Hybrid repair of multiple subclavian and axillary artery aneurysms in a patient with Marfan syndrome
Q30443053	Hypercoagulability in a patient with Marfan syndrome
Q53381873	Iatrogenic acute aortic dissection in a patient with Marfan syndrome: unusual site of intimal tear.
Q88586895	Identification and characterization of a novel FBN1 gene variant in an extended family with variable clinical phenotype of Marfan syndrome
Q57199370	Identification of 23TGFBR2and 6TGFBR1gene mutations and genotype-phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys-Dietz syndrome and related disorders
Q78055586	Identification of 9 novel FBN1 mutations in German patients with Marfan syndrome
Q51409148	Identification of FBN1 gene mutations in Ukrainian Marfan syndrome patients.
Q34516246	Identification of Loci Modulating the Cardiovascular and Skeletal Phenotypes of Marfan Syndrome in Mice
Q35706603	Identification of Marfan syndrome in primary care. Prompt referral can reduce morbidity and mortality.
Q90494803	Identification of Three Novel FBN1 Mutations and Their Phenotypic Relationship of Marfan Syndrome
Q30407859	Identification of a novel FBN1 gene mutation in a Chinese family with Marfan syndrome
Q35651899	Identification of defects in the fibrillin gene and protein in individuals with the Marfan syndrome and related disorders
Q51747020	Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis.
Q84077732	Identification of novel FBN1 and TGFBR2 mutations in 65 probands with Marfan syndrome or Marfan-like phenotypes
Q49102917	Identification of sixty-two novel and twelve known FBN1 mutations in eighty-one unrelated probands with Marfan syndrome and other fibrillinopathies.
Q34977871	Identify and manage marfan syndrome in children
Q79186598	Images in cardiovascular medicine. Simultaneous "Tirone David-V" valve-sparing aortic root replacement and radical mitral valve repair for the Marfan syndrome with Barlow syndrome
Q53426507	Images in vascular medicine. Marfan syndrome - aortic dissection type A, visualized by computed tomography angiography.
Q28235816	Imaging of Marfan syndrome: multisystemic manifestations
Q57167351	Imaging of the Postsurgical Aorta in Marfan Syndrome
Q38887520	Imaging, Endoscopic and Genetic Assessment of Marfan Syndrome Presenting with Sigmoid Volvulus: A Review
Q92021673	Imaging-Based 4D Aortic Pressure Mapping in Marfan Syndrome Patients: A Matched Case-Control Study (Commentary)
Q90377407	Imaging-Based 4D Aortic Pressure Mapping in Marfan Syndrome Patients: A Matched Case-Control Study
Q84165326	Immediate effects of submaximal effort on pulse wave velocity in patients with Marfan syndrome
Q33233846	Immunohistochemical evaluation of conjunctival fibrillin-1 in Marfan syndrome
Q72420839	Immunohistochemical localization of fibrillin in human ocular tissues. Relevance to the Marfan syndrome
Q68522031	Immunohistologic abnormalities of the microfibrillar-fiber system in the Marfan syndrome
Q88923363	Impact of Pathogenic FBN1 Variant Types on the Progression of Aortic Disease in Patients With Marfan Syndrome
Q85541071	Impact of age and gender on cardiac pathology in children and adolescents with Marfan syndrome
Q45279577	Impact of aortic aneurysm on hospitalizations in patients with marfan syndrome: a multi-institutional study
Q77369184	Impact of laboratory molecular diagnosis on contemporary diagnostic criteria for genetically transmitted cardiovascular diseases: hypertrophic cardiomyopathy, long-QT syndrome, and marfan syndrome : A statement for healthcare professionals from the
Q58862384	Impaired Biventricular Deformation in Marfan Syndrome: A Strain and Strain Rate Study in Adult Unoperated Patients
Q81993804	Impaired right ventricular systolic function demonstrated by reduced atrioventricular plane displacement in adults with Marfan syndrome
Q91069599	Impaired vascular smooth muscle cell force-generating capacity and phenotypic deregulation in Marfan Syndrome mice
Q88641619	Importance of Early Detection and Cardiovascular Surgical Intervention in Marfan Syndrome
Q95373499	Importance of Early Detection and Cardiovascular Surgical Intervention in Marfan Syndrome
Q33292654	In vivo corneal confocal microscopy in marfan syndrome
Q47759414	Inadequate spinal anesthesia in a patient with marfan syndrome and dural ectasia
Q91311876	Incidence of cardiovascular events and risk markers in a prospective study of children diagnosed with Marfan syndrome
Q97643002	Increase in dural ectasia size in scoliosis patients with Marfan syndrome
Q90721491	Increased fracture rate in children and adolescents with Marfan syndrome
Q91920249	Increased frequency of FBN1 frameshift and nonsense mutations in Marfan syndrome patients with aortic dissection
Q49053501	Increased frequency of FBN1 truncating and splicing variants in Marfan syndrome patients with aortic events.
Q91951048	Increased visceral arterial tortuosity in Marfan syndrome
Q40074480	Indomethacin Prevents the Progression of Thoracic Aortic Aneurysm in Marfan Syndrome Mice
Q33925296	Induction of macrophage chemotaxis by aortic extracts from patients with Marfan syndrome is related to elastin binding protein
Q36660642	Infantile Marfan syndrome in a Korean tertiary referral center
Q41809655	Infectious endocarditis complicated by an ischemic stroke and revealing Marfan syndrome
Q40083565	Infective endocarditis caused by Pseudomonas stutzeri in a patient with Marfan syndrome: Case report and brief literature review
Q34221265	Inflammation aggravates disease severity in Marfan syndrome patients.
Q43236582	Informative STR Markers for Marfan Syndrome in Birjand, Iran.
Q40031014	Inhibited Maturation of Collagen in Lathyrism as a Model for the Marfan Syndrome and its Implications
Q50057280	Inhibition of Marfan Syndrome Aortic Root Dilation by Losartan: Role of Angiotensin II Receptor Type 1-Independent Activation of Endothelial Function.
Q101568702	Inhibition of transforming growth factor-β signaling in myeloid cells ameliorates aortic aneurysmal formation in Marfan syndrome
Q33168875	Inpatient rehabilitation for adult patients with Marfan syndrome: an observational pilot study
Q90717771	Institutional Marfan syndrome surgical volume influences mitral valve surgical strategy in patients with Marfan syndrome
Q93017157	Intercalary staphyloma in Marfan syndrome: A dreaded complication of scleral incision
Q74521262	Internal mammary artery aneurysm in Marfan syndrome: case report
Q40300791	Interpretation of sequence variants of the FBN1 gene: analog or digital? A commentary on decreased frequency of FBN1 missense variants in Ghent criteria-positive Marfan syndrome and characterization of novel FBN1 variants
Q87687632	Interventional Spine Considerations for Dural Ectasia in a Patient With Marfan Syndrome
Q104062142	Intracranial Aneurysms Are Associated With Marfan Syndrome: Single Cohort Retrospective Study in 118 Patients Using Brain Imaging
Q98581116	Intracranial Arterial Tortuosity in Marfan Syndrome and Loeys-Dietz Syndrome: Tortuosity Index Evaluation Is Useful in the Differential Diagnosis
Q80918023	Intracranial hypertension in 2 children with marfan syndrome
Q31131657	Intracranial hypotension in a girl with Marfan syndrome: case report and review of the literature.
Q83139315	Intrafamilial phenotype variation in Marfan syndrome ascertained by intragenic linkage analysis
Q48179118	Intrinsic cardiomyopathy in Marfan syndrome: results from in-vivo and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humans.
Q80499414	Investigation of muscle bioenergetics in the Marfan syndrome indicates reduced metabolic efficiency
Q91969017	Irbesartan in Marfan syndrome (AIMS): a double-blind, placebo-controlled randomised trial
Q73317456	Iridocorneal adhesions in patients with the Marfan syndrome
Q40941227	Is Marfan syndrome associated with symptomatic intracranial aneurysms?
Q81513468	Is fatigue in Marfan syndrome related to orthostatic intolerance?
Q83277086	Isolated cleft of the posterior mitral valve leaflet in a patient with Marfan syndrome
Q80177110	Isolated distal coronary dissection in Marfan syndrome
Q42343439	Kid-Short Marfan Score (Kid-SMS) Is a Useful Diagnostic Tool for Stratifying the Pre-Test Probability of Marfan Syndrome in Childhood
Q67556094	L-thyroxine therapy for congenital hypothyroidism and Marfan syndrome
Q21144449	LRP1 functions as an atheroprotective integrator of TGFbeta and PDFG signals in the vascular wall: implications for Marfan syndrome
Q89952181	Large Family With Marfan Syndrome Demonstrating the Pathogenicity of a "Synonymous" Variant (p.Ile2118=) in the Fibrillin-1 Gene
Q35941351	Large ascending aortic aneurysm and severe aortic regurgitation in a 7-year-old child with Marfan syndrome and a review of the literature. Marfan syndrome in childhood
Q80305336	Large genomic fibrillin-1 (FBN1) gene deletions provide evidence for true haploinsufficiency in Marfan syndrome
Q36813218	Large pseudo aneurysm due to ruptured ostial coronary button after Bentall procedure in a patient with Marfan syndrome
Q34175314	Large pulmonary artery aneurysm associated with Marfan syndrome
Q84762266	Large-sized bilateral axillary artery aneurysms in a patient with marfan syndrome: a case report
Q39219224	Late diagnosis of Marfan syndrome with fatal outcome in a young male patient: a case report
Q47359345	Lateral Position for Cesarean Delivery Because of Severe Aortocaval Compression in a Patient With Marfan Syndrome: A Case Report.
Q41505830	Left gastric artery aneurysm in Marfan syndrome: a unique case
Q100636751	Left parasternal approach for Bentall procedure in a patient of Marfan syndrome with severe pectus excavatum
Q72119300	Left ventricular function in children with the Marfan syndrome
Q43604647	Left ventricular function in the Marfan syndrome without significant valvular regurgitation
Q35527297	Left ventricular systolic dysfunction in asymptomatic Marfan syndrome patients is related to the severity of gene mutation: insights from the novel three dimensional speckle tracking echocardiography
Q78456721	Leg-length discrepancy and scoliosis in Marfan syndrome
Q70140172	Length polymorphism in the pro alpha 2(I) collagen gene: an alternative explanation in a case of Marfan syndrome
Q73269890	Lens Dislocation in Marfan Syndrome and UV-B Light Exposure
Q74243539	Lens dislocation in Marfan syndrome: potential role of matrix metalloproteinases in fibrillin degradation
Q92716117	Lensectomy Vitrectomy for Ectopia Lentis and Rhegmatogenous Retinal Detachment in a Patient With Marfan Syndrome
Q79847774	Lessons from Marfan syndrome
Q52828565	Letter: Collagen of Marfan syndrome is abnormally soluble.
Q67289418	Life Expectancy and Causes of Death in the Marfan Syndrome
Q50863710	Life expectancy in British Marfan syndrome populations.
Q57222332	Life expectancy in the Marfan syndrome
Q37577831	Like Father, Like Daughter-inherited cutis aplasia occurring in a family with Marfan syndrome: a case report.
Q93665024	Lincoln and the Marfan Syndrome
Q54269876	Lincoln and the Marfan Syndrome: The Medical Diagnosis of a Historical Figure.
Q52415534	Lincoln did not have the Marfan Syndrome; documented evidence.
Q33597154	Linkage analysis of five fibrillar collagen loci in a large French Marfan syndrome family
Q33495349	Linkage data for Marfan syndrome and markers on chromosomes 1 and 11.
Q34592768	Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes
Q36543403	Lipid storage myopathy with clinical markers of Marfan syndrome: A rare association
Q52128037	Living with Marfan syndrome I. Perceptions of the condition.
Q52128036	Living with Marfan syndrome II. Medication adherence and physical activity modification.
Q52115012	Living with Marfan syndrome III. Quality of life and reproductive planning.
Q53620319	Living with Marfan syndrome: coping with stigma.
Q94601749	Localized Antileptin Therapy Prevents Aortic Root Dilatation and Preserves Left Ventricular Systolic Function in a Murine Model of Marfan Syndrome
Q68923094	Location on chromosome 15 of the gene defect causing Marfan syndrome
Q50180892	Long-Term Results of Aortic Root Surgery in Marfan Syndrome Patients: A Single-Center Experience.
Q96436632	Long-term clinical outcomes of losartan in patients with Marfan syndrome: follow-up of the multicentre randomized controlled COMPARE trial
Q46664663	Long-term doxycycline is more effective than atenolol to prevent thoracic aortic aneurysm in marfan syndrome through the inhibition of matrix metalloproteinase-2 and -9.
Q83524124	Long-term follow-up after bilateral Artisan aphakia intraocular lens implantation in two children with Marfan syndrome
Q35678335	Long-term implications of emergency versus elective proximal aortic surgery in patients with Marfan syndrome in the Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions Consortium Registry
Q44690318	Long-term outcome in patients with Marfan syndrome: is aortic dissection the only cause of sudden death?
Q99572851	Long-term outcome of patients with Marfan syndrome with previous aortic surgery but native aortic roots
Q34674968	Long-term outcomes of aortic root operations for Marfan syndrome: A comparison of Bentall versus aortic valve-sparing procedures
Q90337190	Long-term outcomes of aortic valve reimplantation in Marfan syndrome
Q91792712	Long-term outcomes of surgical procedures for Marfan syndrome: aortic dissection versus aneurysm
Q74705142	Long-term prognosis of surgically-treated aortic aneurysms and dissections in patients with and without Marfan syndrome
Q43657667	Long-term results of aortic root replacement for Marfan syndrome
Q30842639	Longitudinal Evaluation of Aortic Hemodynamics in Marfan Syndrome: New Insights from a 4D Flow Cardiovascular Magnetic Resonance Multi-Year Follow-Up Study
Q88923369	Looking for the Missing Links: Challenges in the Search for Genotype-Phenotype Correlation in Marfan Syndrome
Q57046911	Losartan Versus Atenolol for Prevention of Aortic Dilation in Patients With Marfan Syndrome
Q38457559	Losartan added to β-blockade therapy for aortic root dilation in Marfan syndrome: a randomized, open-label pilot study.
Q90674006	Losartan for Preventing Aortic Root Dilatation in Patients with Marfan Syndrome: A Meta-Analysis of Randomized Trials
Q57046905	Losartan for the Treatment of Marfan Syndrome: Hope Fades
Q88813049	Losartan in combination with propranolol slows the aortic root dilatation in neonatal Marfan syndrome
Q44212007	Losartan reduces aortic dilatation rate in adults with Marfan syndrome: a randomized controlled trial
Q33692258	Losartan therapy in adults with Marfan syndrome: study protocol of the multi-center randomized controlled COMPARE trial
Q87350961	Losartan treatment in adult patients with Marfan syndrome: can we finally COMPARE?
Q24548457	Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome
Q80642355	Loss of elastic fiber integrity and reduction of vascular smooth muscle contraction resulting from the upregulated activities of matrix metalloproteinase-2 and -9 in the thoracic aortic aneurysm in Marfan syndrome
Q21203044	Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
Q71768663	Lumbar spine in Marfan syndrome
Q81575155	Lymphoma presenting as chronic aortic dissection in Marfan syndrome
Q69878290	Lysyl oxidase activity and synthesis of desmosines in cultured human aortic cells and skin fibroblasts: comparison of cell lines from control subjects and patients with the Marfan syndrome or other annulo-aortic ectasia
Q57255668	MARFAN SYNDROME RELATED TO TGFβR2 MUTATION AND SUDDEN DEATH: A ROLE FOR ABNORMAL VENTRICULAR REPOLARIZATION RELATED ARRHYTHMIAS?
Q36509102	MARFAN SYNDROME, DISSECTING ANEURYSM OF THE AORTA, AND PREGNANCY
Q34171036	MMP-2 regulates Erk1/2 phosphorylation and aortic dilatation in Marfan syndrome
Q81191462	MR evaluation of dural ectasia in Marfan syndrome: reassessment of the established criteria in children, adolescents, and young adults
Q87352404	MRI-assessed regional pulse wave velocity for predicting absence of regional aorta luminal growth in marfan syndrome
Q57011307	Magnetic resonance imaging evaluation of aortic elastic properties as early expression of Marfan syndrome
Q51680678	Magnetic resonance microscopy quantifies the disease progression in Marfan syndrome mice.
Q96234598	Male-female differences in quality of life and coping style in patients with Marfan syndrome and hereditary thoracic aortic diseases
Q69207742	Malignant quadrivalvular dysplasia of Marfan syndrome in a neonate
Q64227528	Management Strategies of Ocular Abnormalities in Patients with Marfan Syndrome: Current Perspective
Q92964081	Management and Outcomes of Aortic Dissection in Pregnancy with Marfan syndrome: A Systematic Review
Q59275285	Management of Aortic Disease in Marfan Syndrome
Q38729253	Management of Marfan Syndrome during pregnancy: A real world experience from a Joint Cardiac Obstetric Service.
Q99709805	Management of a giant aortic root aneurysm in a young patient with Marfan syndrome: a case report
Q72436555	Management of cardiovascular complications in Marfan syndrome
Q61648337	Management of mitral regurgitation in Marfan syndrome: Outcomes of valve repair versus replacement and comparison with myxomatous mitral valve disease
Q38223327	Management of the pregnant woman with Marfan syndrome complicated by ascending aorta dilation
Q99576014	Management of unilateral temporomandibular joint ankylosis & orthomorphic correction in a patient with Marfan syndrome: A rare case report
Q88427299	Marfan Syndrome (MFS): Visual Diagnosis and Early Identification
Q90817288	Marfan Syndrome - Acute Aortic Dissection Due to Giant Aortic Aneurysm
Q89105320	Marfan Syndrome Caused by Somatic Mosaicism in an FBN1 Splicing Mutation
Q48252149	Marfan Syndrome Presenting as Giant Bullous Emphysema
Q58726367	Marfan Syndrome Variability: Investigation of the Roles of Sarcolipin and Calcium as Potential Transregulator of FBN1 Expression
Q93189235	Marfan Syndrome Versus Bicuspid Aortic Valve Disease: Comparative Analysis of Obstetric Outcome and Pregnancy-Associated Immediate and Long-Term Aortic Complications
Q53838192	Marfan Syndrome and Loeys-Dietz Syndrome in Children: A Multidisciplinary Team Experience.
Q38735759	Marfan Syndrome and Quality of Life in the GenTAC Registry
Q38751533	Marfan Syndrome and Related Disorders: 25 Years of Gene Discovery.
Q38573750	Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections
Q44487355	Marfan Syndrome, Pregnancy, and Fatal Dissection of Aorta
Q81452067	Marfan Syndrome, aortic dissection and the EMS provider
Q53097937	Marfan Syndrome: A Clinical Update.
Q36947965	Marfan Syndrome: A Review and Update
Q88284428	Marfan Syndrome: Always Evolving
Q38169124	Marfan Syndrome: Clinical, Surgical, and Anesthetic Considerations
Q41953262	Marfan Syndrome: Correct diagnosis can save lives
Q41435213	Marfan Syndrome: Exclusion of genetic linkage to three major collagen genes
Q54426541	Marfan Syndrome: Staging Nonsurgical vs Surgical Treatments in Children With Subluxated Lenses and Refractive Problems.
Q38876867	Marfan Syndrome: new diagnostic criteria, same anesthesia care? Case report and review
Q55360933	Marfan Syndrome: oral implication and management.
Q85160857	Marfan Syndrome: when to operate TAA(A)s?
Q28257268	Marfan syndrome
Q37106238	Marfan syndrome affecting a whole Sudanese family
Q36681743	Marfan syndrome affecting four generations of a family without ocular involvement
Q70480125	Marfan syndrome and aortic aneurysm
Q52934691	Marfan syndrome and aortic aneurysm: Lysyl oxidases to the rescue?
Q83665580	Marfan syndrome and aortic dissection in pregnancy
Q41065296	Marfan syndrome and cardiovascular complications: results of a family investigation.
Q46563598	Marfan syndrome and cervical internal carotid artery aneurysm
Q44376338	Marfan syndrome and cystic kidneys of the adult type
Q69656269	Marfan syndrome and dilated aortic root--clinical findings, diagnosis and case reports
Q66931351	Marfan syndrome and dissecting ruptured aneurysm in pregnancy
Q73520427	Marfan syndrome and dural ectasia: a common, yet little known association
Q72837741	Marfan syndrome and echocardiography
Q34121719	Marfan syndrome and fibrillin disorders
Q43001562	Marfan syndrome and focal segmental glomerulosclerosis: a novel association
Q73232894	Marfan syndrome and intracranial aneurysms
Q37387172	Marfan syndrome and its disorder in periodontal tissues
Q57519912	Marfan syndrome and liability to psychosis
Q70647312	Marfan syndrome and medullary sponge kidney: case report and speculation on pathogenesis
Q37625971	Marfan syndrome and mitral valve prolapse
Q50561098	Marfan syndrome and other systemic disorders with congenital ectopia lentis. A Danish national survey.
Q71068968	Marfan syndrome and pituitary dwarfism
Q87443644	Marfan syndrome and pneumothorax
Q41702849	Marfan syndrome and pregnancy
Q35931816	Marfan syndrome and pregnancy - a district hospital perspective
Q44116853	Marfan syndrome and pregnancy. Apropos of 4 cases
Q34174696	Marfan syndrome and pregnancy: maternal and neonatal outcomes
Q48091561	Marfan syndrome and pregnancy:monitoring and management
Q43751954	Marfan syndrome and related connective tissue disorders
Q91528769	Marfan syndrome and related connective tissue disorders in the current era in Switzerland in 103 patients: medical and surgical management and impact of genetic testing
Q81518725	Marfan syndrome and related disorders
Q71846163	Marfan syndrome and retinopathia pigmentosa
Q71863509	Marfan syndrome and retroperitoneal fibrosis
Q35659320	Marfan syndrome and schizophrenia: a case report and literature review
Q70752703	Marfan syndrome and similar genetic disorders. I. The Marfan syndrome
Q81115778	Marfan syndrome and sudden death within a family - aetiologic, molecular and diagnostic issues at autopsy
Q50254805	Marfan syndrome and sudden death.
Q42105049	Marfan syndrome and symptomatic sacral cyst: report of two cases
Q34518714	Marfan syndrome and the 18th dynasty royal family of ancient Egypt. Preliminary research report [Part II]
Q37699032	Marfan syndrome and the evolving spectrum of heritable thoracic aortic disease: do we need genetics for clinical decisions?
Q86026142	Marfan syndrome and the thumb sign
Q38047208	Marfan syndrome and vascular dissections during pregnancy
Q54329837	Marfan syndrome as a paradigm for transcript-targeted preimplantation diagnosis of heterozygous mutations.
Q50100741	Marfan syndrome as a predisposing factor for traumatic aortic insufficiency.
Q38914815	Marfan syndrome associated aortic disease in neonates and children: a clinical-morphologic review
Q71104939	Marfan syndrome associated with beta-thalassemia
Q68615804	Marfan syndrome associated with bicuspid aortic valve, premature aging, and primary hypogonadism
Q74124846	Marfan syndrome associated with moyamoya phenomenon and aortic dissection
Q43794985	Marfan syndrome caused by a mutation in FBN1 that gives rise to cryptic splicing and a 33 nucleotide insertion in the coding sequence
Q59615697	Marfan syndrome caused by a novel FBN1 mutation with associated pigmentary glaucoma
Q55671357	Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
Q58739469	Marfan syndrome combined with huge abdominal aortic aneurysm size of 20 × 11 cm: A case report of surgical approach
Q85419882	Marfan syndrome database information unreliable for diagnoses
Q85167619	Marfan syndrome decreases Ca2+ wave frequency and vasoconstriction in murine mesenteric resistance arteries without changing underlying mechanisms
Q47911572	Marfan syndrome diagnosed in patients 32 years of age or older
Q68916110	Marfan syndrome gene search intensifies following identification of basic defect
Q37972094	Marfan syndrome in China: a collective review of 564 cases among 98 families
Q70320760	Marfan syndrome in Chinese
Q49122898	Marfan syndrome in Europe.
Q81557194	Marfan syndrome in South Africa: a molecular genetic approach to diagnosis
Q48226314	Marfan syndrome in a Triple-X girl: a new association?
Q34246137	Marfan syndrome in a female collegiate basketball player: a case report.
Q33593710	Marfan syndrome in a large family: response of family members to a screening programme
Q93191133	Marfan syndrome in a term-pregnant woman with aortic root dilatation between 40 and 45 mm
Q70893999	Marfan syndrome in aboriginals
Q90761956	Marfan syndrome in adolescence: adolescents' perspectives on (physical) functioning, disability, contextual factors and support needs
Q41190455	Marfan syndrome in adolescents and young adults: psychosocial functioning and knowledge
Q42737144	Marfan syndrome in an Iranian family: a case series
Q92260252	Marfan syndrome in childhood: parents' perspectives of the impact on daily functioning of children, parents and family; a qualitative study
Q45198749	Marfan syndrome in children
Q35366309	Marfan syndrome in children and adolescents: an adjusted nomogram for screening aortic root dilatation.
Q35368617	Marfan syndrome in children and adolescents: predictive and prognostic value of aortic root growth for screening for aortic complications.
Q99548346	Marfan syndrome in children: correlation between musculoskeletal features and cardiac Z-score
Q41635431	Marfan syndrome in pregnancy
Q79405462	Marfan syndrome in pregnancy: a case report
Q69682547	Marfan syndrome in the parturient
Q34982429	Marfan syndrome in the third Millennium
Q38394391	Marfan syndrome is associated with recurrent dissection of the dissected aorta
Q37516648	Marfan syndrome is closely linked to a marker on chromosome 15q1.5----q2.1.
Q78095052	Marfan syndrome is not associated with intracranial aneurysms
Q41328233	Marfan syndrome is the main independent predictor of recurrent aortic dissection in patients enrolled in the International Registry of Aortic Dissection (IRAD).
Q37378678	Marfan syndrome masked by Down syndrome?
Q42559783	Marfan syndrome or Marfan-like connective-tissue disorder
Q85899888	Marfan syndrome patient experiences as ascertained through postings on social media sites
Q39717511	Marfan syndrome presenting as aortic rupture in a young athlete: sudden unexpected death?
Q73573283	Marfan syndrome presenting as fatal ruptured dissecting aneurysm of aorta
Q50069582	Marfan syndrome presenting with diffuse emphysematous change of the lung.
Q36745912	Marfan syndrome presenting with headache and coincidental ophthalmic artery aneurysm
Q53020562	Marfan syndrome presenting with postpartum aortic dissection following dural puncture headache and epidural blood patch.
Q73621797	Marfan syndrome presenting with transient renal insufficiency
Q95310099	Marfan syndrome revisited: From genetics to the clinic
Q30456524	Marfan syndrome teaching algorithm: does it make a difference?
Q67387575	Marfan syndrome treated with propranolol
Q49027700	Marfan syndrome type II: there is more to Marfan syndrome than fibrillin 1.
Q35920090	Marfan syndrome with a complex chromosomal rearrangement including deletion of the FBN1 gene
Q55122834	Marfan syndrome with a giant noncoronary sinus of Valsalva aneurysm.
Q88358453	Marfan syndrome with a homozygous FBN1 splicing mutation
Q39811896	Marfan syndrome with acute abdomen: a case report
Q45878256	Marfan syndrome with antineutrophil cytoplasmic antibody-associated systemic vasculitis presenting as severe anaemia and haematuria after the Bentall procedure
Q68200922	Marfan syndrome with aortic dissection and triple-barrel aorta
Q38069303	Marfan syndrome with ascending aortic aneurysm: value of cardiac computed tomography
Q71134674	Marfan syndrome with back pain secondary to pedicular attenuation
Q71967958	Marfan syndrome with back pain secondary to pedicular attenuation. A case report
Q39771288	Marfan syndrome with congenital contractures
Q67329197	Marfan syndrome with contractural arachnodactyly and severe mitral regurgitation in a premature infant
Q42068134	Marfan syndrome with coronary artery lesions in a North American Indian
Q67763840	Marfan syndrome with dissecting aneurysm of the aorta comprising the oesophagus (author's transl)
Q71042892	Marfan syndrome with microcornea, aphakia and ventricular septal defect. Case report
Q40759788	Marfan syndrome with multiseptate pneumothorax and mandibular fibrous dysplasia
Q72924016	Marfan syndrome with myocarditis demonstrated by 99Tcm-HMPAO-labelled WBC and 201Tl scintigraphy: report of three cases in a Chinese family
Q52900776	Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3' terminus of the FBN1-gene.
Q47662906	Marfan syndrome with pneumothorax: case report and review of literatures
Q46558547	Marfan syndrome with spontaneous rupture of aneurysm of common iliac artery
Q53692793	Marfan syndrome with type - 1 diabetes and pulmonary tuberculosis - A rare case.
Q64041313	Marfan syndrome with type 2 diabetes mellitus: A case report from China
Q80969727	Marfan syndrome, MPGN, and bacterial endocarditis
Q77385961	Marfan syndrome, aortic dilatation, and pregnancy
Q97543146	Marfan syndrome, aortic dissection, and pregnancy-the triple combination
Q66905024	Marfan syndrome, arachnodactyly, and cardiac abnormalities
Q67600620	Marfan syndrome, hypertrophic cardiomyopathy findings underline avoidance of some sports
Q87013095	Marfan syndrome, inherited aortopathies and exercise: What is the right answer?
Q38441775	Marfan syndrome, inherited aortopathies and exercise: what is the right answer?
Q73287946	Marfan syndrome, lens subluxation, and open-angle glaucoma
Q35123225	Marfan syndrome, magnesium status and medical prevention of cardiovascular complications by hemodynamic treatments and antisense gene therapy
Q77782026	Marfan syndrome, not Marfan's syndrome
Q69859093	Marfan syndrome, recurrent preterm labour and grandmultiparity
Q71537583	Marfan syndrome. Onset and development of cardiovascular lesions in Marfan syndrome
Q82565336	Marfan syndrome: 30 years of research equals 30 years of additional life expectancy
Q54398793	Marfan syndrome: A case report.
Q92706325	Marfan syndrome: A therapeutic challenge for long-term care
Q28255763	Marfan syndrome: An eyesight of syndrome
Q91873387	Marfan syndrome: Evolving organ manifestations-A 10-year follow-up study
Q88309418	Marfan syndrome: Report of a complex phenotype due to a 15q21.1 contiguos gene deletion encompassing FBN1, and literature review
Q38072937	Marfan syndrome: a case report
Q93226357	Marfan syndrome: a case report and pictorial essay
Q69385527	Marfan syndrome: a collagen disorder?
Q46155729	Marfan syndrome: a diagnostic dilemma
Q41636956	Marfan syndrome: a mystery solved
Q34629629	Marfan syndrome: a review
Q38131783	Marfan syndrome: a review of the literature and case report
Q37575160	Marfan syndrome: a study of a Nigerian family and review of current cardiovascular management.
Q36384445	Marfan syndrome: abnormal alpha 2 chain in type I collagen
Q68347463	Marfan syndrome: absence of type I or III collagen structural defects in 25 patients
Q34628332	Marfan syndrome: an update of genetics, medical and surgical management
Q48743544	Marfan syndrome: clinical consequences resulting from a medicolegal autopsy of a case of sudden death due to aortic rupture.
Q34579317	Marfan syndrome: clinical diagnosis and management
Q37801896	Marfan syndrome: clinical manifestations, pathophysiology and new outlook on drug therapy.
Q40871294	Marfan syndrome: current and future clinical and genetic management of cardiovascular manifestations
Q26747739	Marfan syndrome: current perspectives
Q35596012	Marfan syndrome: defective synthesis, secretion, and extracellular matrix formation of fibrillin by cultured dermal fibroblasts
Q69549804	Marfan syndrome: demonstration of abnormal elastic fibers in skin
Q70073466	Marfan syndrome: dental problems and management
Q44685092	Marfan syndrome: evaluation with MR imaging versus CT.
Q68083332	Marfan syndrome: exclusion of genetic linkage to five genes coding for connective tissue components in the long arm of chromosome 2
Q69892622	Marfan syndrome: exclusion of genetic linkage to the COL1A2 gene
Q42660234	Marfan syndrome: fibrillin expression and microfibrillar abnormalities in a family with predominant ocular defects
Q38019328	Marfan syndrome: from gene to therapy
Q36805480	Marfan syndrome: from molecular pathogenesis to clinical treatment
Q40770225	Marfan syndrome: genetic basis and clinical manifestations.
Q33689113	Marfan syndrome: identification and management
Q90681940	Marfan syndrome: improved clinical history results in expanded natural history
Q43145462	Marfan syndrome: light at the end of the tunnel?
Q36137042	Marfan syndrome: literature review of mortality studies
Q52249970	Marfan syndrome: neuropsychological aspects.
Q33708680	Marfan syndrome: new clues to genotype-phenotype correlations
Q35196800	Marfan syndrome: no evidence for heterogeneity in different populations, and more precise mapping of the gene
Q39846037	Marfan syndrome: ocular findings and novel mutations-in pursuit of genotype-phenotype associations.
Q34553289	Marfan syndrome: orthopedic and genetic review
Q27029752	Marfan syndrome: report of two cases with review of literature
Q35165120	Marfan syndrome: screening for sudden death in athletes
Q72595207	Marfan syndrome: the variability and outcome of operative management
Q36266031	Marfan syndrome: what internists and pediatric or adult cardiologists need to know
Q53122946	Marfan syndrome; A connective tissue disease at the crossroads of mechanotransduction, TGFβ signaling and cell stemness.
Q72116682	Marfan's syndrome and mitroaortic disease (apropos of a case)
Q72316355	Massive aneurysm of the thoracic aorta in an infant--a forme fruste of infantile Marfan syndrome
Q70574051	Massive perigraft aortic aneurysm late after composite graft replacement of the ascending aorta and aortic valve in the Marfan syndrome
Q80887378	Massive retrograde acute type B aortic dissection in a postpartum woman with a family history of Marfan syndrome
Q92298088	Maternal and fetal outcomes in pregnancies complicated by Marfan syndrome
Q101057047	Maternal, pregnancy, and neonatal outcomes for women with Marfan syndrome
Q73582751	Maze procedure in the Marfan syndrome
Q71411880	Meatoplasty in Marfan syndrome
Q46796460	Mechanical and pharmacological approaches to investigate the pathogenesis of Marfan syndrome in the abdominal aorta
Q77106229	Mechanisms of aortic valve incompetence: finite-element modeling of Marfan syndrome
Q90413391	Medical management of aortic disease in children with Marfan syndrome
Q37112411	Medical treatment of Marfan syndrome: a time for change.
Q26823672	Medical treatment of aortic aneurysms in Marfan syndrome and other heritable conditions
Q84363982	Medical treatment of crystalline lens dislocation into the anterior chamber in a patient with Marfan syndrome
Q54263355	Medicine. Frightening risk of Marfan syndrome, and potential treatment, elucidated.
Q72059437	Metacarpophalangeal pattern profile analysis in Sotos and Marfan syndrome
Q57978100	Metacarpophalangeal pattern profile in Marfan syndrome and Marfan-like patients
Q62819649	MicroCT imaging reveals differential 3D micro-scale remodelling of the murine aorta in ageing and Marfan syndrome
Q98778900	Microarray analysis of long non-coding RNA expression profiles in Marfan syndrome
Q73269868	Microcornea and Subluxated Lenses Due to a Splicing Error in the Fibrillin-1 Gene in a Patient With Marfan Syndrome
Q93188604	Microcornea and bilateral ectopia lentis in an infant: unusual severe ocular presentation of neonatal Marfan syndrome
Q52538954	Microfibril abnormalities of the lens capsule in patients with Marfan syndrome and ectopia lentis.
Q84245912	Mid-term results of different aortic valve-sparing procedures in Marfan syndrome
Q30277701	Midterm Survival and Quality of Life After Extent II Thoracoabdominal Aortic Repair in Marfan Syndrome
Q38849067	Mild aerobic exercise blocks elastin fiber fragmentation and aortic dilatation in a mouse model of Marfan syndrome associated aortic aneurysm
Q49404326	Minimally Invasive Mitral Valve Repair in a Woman with Marfan Syndrome and Type B Dissection.
Q39828386	Minimally invasive cardiac surgery for a young woman with Marfan syndrome and mitral regurgitation
Q37682355	Minimally invasive repair of pectus excavatum in patients with Marfan syndrome and marfanoid features
Q72250031	Missense mutations impair intracellular processing of fibrillin and microfibril assembly in Marfan syndrome
Q87166349	Missense mutations in FBN1 exons 41 and 42 cause Weill-Marchesani syndrome with thoracic aortic disease and Marfan syndrome
Q77458890	Missense mutations of the fibrillin-1 gene in two Chinese patients with severe Marfan syndrome
Q67995751	Mitral insufficiency and Marfan syndrome in children
Q66923277	Mitral insufficiency in an incomplete form of Marfan syndrome corrected with valve replacement
Q37922113	Mitral valve disease in Marfan syndrome and related disorders.
Q45190988	Mitral valve disease in patients with Marfan syndrome undergoing aortic root replacement
Q82825593	Mitral valve prolapse in Marfan syndrome: an old topic revisited
Q71761759	Mitral valve prolapse in a case of Marfan syndrome with congenital cardiac disease, chronic obstructive pulmonary disease and schizophrenia
Q74143765	Mitral valve replacement and subsequent composite graft replacement of the aortic root for infantile Marfan syndrome
Q80205275	Mitral valve replacement in patient with absent right superior vena cava, pectus excavatum, Marfan syndrome and severe mitral regurgitation
Q82604952	Mitral valve surgery in the adult Marfan syndrome patient
Q84572312	Modified "stent-graft sandwich" technique for treatment of isolated common iliac artery aneurysm in patient with Marfan syndrome
Q88124656	Modified Sleeve Technique in Aortic Valve-Sparing Operation for Marfan Syndrome
Q83962172	Molecular analysis for diagnosis of Marfan syndrome and Marfan-associated disorders
Q68113200	Molecular biology of Marfan syndrome
Q74171915	Molecular effects of calcium binding mutations in Marfan syndrome depend on domain context
Q28247558	Molecular genetics of Marfan syndrome
Q47897514	Molecular genetics of Marfan syndrome and Ehlers-Danlos type IV.
Q70454023	More speculation on Marfan syndrome
Q43488156	Morphologic and hist-enzymatic aspects of palmar aponeurosis in a patient with Marfan syndrome associated with Dupuytren's contracture
Q24794448	Multi-exon deletions of the FBN1 gene in Marfan syndrome
Q79451735	Multi-exon out of frame deletion of the FBN1 gene leading to a severe juvenile onset cardiovascular phenotype in Marfan syndrome
Q89218197	Multi-imaging assessment of successful surgical treatment of pulmonary artery dilatation and dissection in Marfan syndrome
Q98943860	Multi-stage open surgical and endovascular treatment of progressive aortic degeneration in a patient with Marfan syndrome
Q43014372	Multi-vessel dissections in Marfan syndrome demonstrated by multislice computed tomography
Q38097295	Multidisciplinary approach to a Marfan syndrome patient with emphasis on cardiovascular complications
Q69258058	Multiple meningeal cysts in Marfan syndrome
Q53294227	Multisegment coloboma in a case of Marfan syndrome: another possible effect of increased TGFβ signaling.
Q35556205	Muscle and Bone Impairment in Children With Marfan Syndrome: Correlation With Age and FBN1 Genotype
Q79847780	Muscle strength and body composition in adult women with Marfan syndrome
Q67297520	Musculoskeletal manifestations of the Marfan syndrome: radiologic features
Q71732096	Mutant fibrillin-1 monomers lacking EGF-like domains disrupt microfibril assembly and cause severe marfan syndrome
Q91296809	Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience
Q64064060	Mutation screening in the FBN1 gene responsible for Marfan syndrome and related disorder in Chinese families
Q57273789	Mutation screening of all 65 exons of the fibrillin-1 gene in 60 patients with Marfan syndrome: Report of 12 novel mutations
Q44195788	Mutation screening of the fibrillin-1 (FBN1) gene in 76 unrelated patients with Marfan syndrome or Marfanoid features leads to the identification of 11 novel and three previously reported mutations
Q40934983	Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders
Q28219544	Mutations of FBN1 and genotype-phenotype correlations in Marfan syndrome and related fibrillinopathies
Q100383592	Myocardial Function, Heart Failure and Arrhythmia in Marfan Syndrome: A Systematic Literature Review
Q100957021	Myocardial disease and ventricular arrhythmia in Marfan syndrome: a prospective study
Q69788280	Myocardial involvement in the Marfan syndrome
Q101241005	Myocardial ischemia 10 years after a modified Cabrol procedure in a 42-year-old patient with Marfan syndrome
Q80645193	Myocardial ischemia due to compression of an unruptured thoracic aortic aneurysm in a patient with Marfan syndrome
Q59045981	NEONATAL MARFAN SYNDROME
Q90178650	NGS analysis in Marfan syndrome spectrum: Combination of rare and common genetic variants to improve genotype-phenotype correlation analysis
Q38996347	Native Mitral Valve Endocarditis Caused by Neisseria elongata subsp. nitroreducens in a Patient with Marfan Syndrome: First Case in Italy and Review of the Literature
Q86259302	Natural course of isolated spontaneous coronary artery dissection in Marfan syndrome
Q74429113	Near-total aortic replacement for acute type A dissection in a patient with Marfan syndrome
Q59045995	Neonatal Marfan Syndrome
Q93016701	Neonatal Marfan Syndrome
Q96582854	Neonatal Marfan Syndrome by Inherited Mutation
Q91748893	Neonatal Marfan Syndrome: A Rare, Severe, and Life-Threatening Genetic Disease
Q36715457	Neonatal Marfan Syndrome: Report of a Case with an Inherited Splicing Mutation outside the Neonatal Domain
Q74442529	Neonatal Marfan syndrome
Q79338161	Neonatal Marfan syndrome : in utero presentation with aortic and pulmonary artery dilatation and successful repair of an acute flail mitral valve leaflet in infancy
Q80404527	Neonatal Marfan syndrome caused by an exon 25 mutation of the fibrillin-1 gene
Q89942125	Neonatal Marfan syndrome diagnosed prenatally
Q53479510	Neonatal Marfan syndrome with angle-closure glaucoma, tricuspid and mitral insufficiency.
Q33596757	Neonatal Marfan syndrome with congenital arachnodactyly, flexion contractures, and severe cardiac valve insufficiency
Q47681976	Neonatal Marfan syndrome: Report of two cases
Q77996457	Neonatal Marfan syndrome: a case report
Q33802533	Neonatal Marfan syndrome: a successful early multidisciplinary approach
Q36071957	Neonatal Marfan syndrome: clinical report and review of the literature.
Q84193215	Neonatal Marfan syndrome: unusually large deletion of exons 24-26 of FBN1 associated with poor prognosis
Q87165794	Neonatal marfan syndrome with hiatus hernia and intrathoracic stomach
Q36617253	Neonatal marfan syndrome: report of two cases
Q34409249	Neonatal progeroid variant of Marfan syndrome with congenital lipodystrophy results from mutations at the 3' end of FBN1 gene
Q69435692	Neurologic manifestations of the Marfan syndrome
Q104506335	Neurophysiological assessment in a patient affected by Marfan syndrome
Q77713295	Neurovascular complications of marfan syndrome: a retrospective, hospital-based study
Q99399952	Neurovascular manifestations in connective tissue diseases: The case of Marfan Syndrome
Q89476009	New Screening Tool for Aortic Root Dilation in Children with Marfan Syndrome and Marfan-Like Disorders
Q31166327	New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome
Q85751002	Next generation sequencing as a rapid molecular diagnosis for Marfan syndrome in a Chinese family with mutations in the fibrillin-1 gene
Q90863882	Non-invasive assessment of endarteritis in Marfan syndrome with aortic dissection after surgical treatment
Q47609083	Non-invasive cardiac output monitoring for cesarean delivery under epidural anesthesia in a patient with Marfan syndrome and cardiomyopathy
Q35034373	Noncanonical TGFβ signaling contributes to aortic aneurysm progression in Marfan syndrome mice
Q37589583	Noninvasive diagnosis and management of spontaneous intracranial hypotension in patients with marfan syndrome: Case Report and Review of the Literature
Q40914843	Nonsyndromic Thoracic Aortic Aneurysm and Dissection: Outcomes With Marfan Syndrome Versus Bicuspid Aortic Valve Aneurysm
Q67575912	Normal elastin content of aorta in bovine Marfan syndrome
Q46460846	Normal regional pulse wave velocity predicts absence of aortic luminal growth in patients with Marfan syndrome: a comprehensive MRI-study
Q86764104	Notice of Retraction: Ahimastos AA, et al. Effect of Perindopril on Large Artery Stiffness and Aortic Root Diameter in Patients With Marfan Syndrome: A Randomized Controlled Trial. JAMA. 2007;298(13):1539-1547
Q93021462	Novel FBN1 Heterozygous Mutations Identified in Chinese Families with Marfan Syndrome
Q49043895	Novel FBN1 mutation causes Marfan syndrome with bilateral ectopia lentis and refractory glaucoma.
Q48099808	Novel FBN1 mutation in a family with inherited Marfan Syndrome: p.Cys2672Arg
Q73623267	Novel approach to the molecular diagnosis of Marfan syndrome: application to sporadic cases and in prenatal diagnosis
Q84920451	Novel de novo nonsense mutation of FBN1 gene in a patient with Marfan syndrome
Q89808856	Novel double-flanged technique for managing Marfan syndrome and microspherophakia
Q56988790	Novel exon skipping mutation in the fibrillin-1 gene: Two 'hot spots' for the neonatal Marfan syndrome
Q46673651	Novel fibrillin 1 mutation in a case of neonatal Marfan syndrome: the increasing importance of early recognition
Q80991031	Novel human pathological mutations. Gene symbol: FBN1. Disease: Marfan syndrome
Q81556931	Novel non-synonymous mutation in the transforming growth factor beta binding protein-like (TB) domain of the fibrillin-1 (FBN1) gene in a Han Chinese family with Marfan syndrome (MFS)
Q88745654	Novel reconstruction of a vascular aneurysm in Marfan syndrome
Q57847415	NovelFBN1gene mutation and maternal germinal mosaicism as the cause of neonatal form of Marfan syndrome
Q35069518	Observational cohort study of ventricular arrhythmia in adults with Marfan syndrome caused by FBN1 mutations
Q72035380	Observations on the fine structure of the fibroblast from a case of Ehlers-Danlos syndrome with the Marfan syndrome
Q59401069	Obstetric and cardiac outcomes in women with Marfan syndrome and an aortic root diameter ≤ 45mm
Q79173685	Obstetric and gynecologic complications in women with Marfan syndrome
Q70672664	Obstetrical complications in a patient with the Marfan syndrome
Q64044032	Obstructive sleep apnea in children with Marfan syndrome: Relationships between three-dimensional palatal morphology and apnea-hypopnea index
Q48826862	Obstructive sleep hypopnea syndrome in a patient with Marfan syndrome treated with oxygen therapy.
Q69383531	Ocular Manifestations in the Marfan Syndrome and Homocystinuria
Q37169409	Ocular features of Marfan syndrome: diagnosis and management.
Q52662416	Ocular manifestation in Marfan syndrome: corneal biomechanical properties relate to increased systemic score points.
Q52806534	Ocular manifestations of Marfan syndrome in children and adolescents.
Q49123758	Ocular manifestations of congenital Marfan syndrome with contractures (CMC syndrome).
Q93758733	Ocular manifestations of the Marfan syndrome
Q84815859	On ten-year epidemiological review of in-hospital patients with Marfan syndrome
Q77953365	Operative management of Marfan syndrome: The Johns Hopkins experience
Q92176685	Optimising Aortic Endovascular Repair in Patients with Marfan Syndrome
Q100572385	Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement
Q58111121	Oral Health-Related Quality of Life in People with Rare Hereditary Connective Tissue Disorders: Marfan Syndrome
Q95646479	Oral health in patients with Marfan syndrome
Q52969581	Oral management of Marfan syndrome: an overview and case report.
Q41599899	Oral manifestations of a rare variant of Marfan syndrome
Q49045290	Oral manifestations of patients with Marfan syndrome: a case-control study.
Q37512554	Orthopaedic Aspects of Marfan Syndrome: The Experience of a Referral Center for Diagnosis of Rare Diseases.
Q81898286	Osteoporosis in adult with Marfan syndrome: casuality or causality?
Q87239152	Outcome of aortic surgery in patients with Loeys-Dietz syndrome primarily treated as having Marfan syndrome
Q69386744	Outcome of pectus excavatum in patients with Marfan syndrome and in the general population
Q89928231	Outcome of sutured scleral fixated intraocular lens in Marfan syndrome in pediatric eyes
Q85491411	Outcomes after valve-preserving root surgery for patients with Marfan syndrome
Q52571936	Overexpression of transforming growth factor-beta is associated with increased hyaluronan content and impairment of repair in Marfan syndrome aortic aneurysm.
Q64026829	Oxidation injury and local mediator interplay in Marfan syndrome
Q91675443	Oxytocin antagonism prevents pregnancy-associated aortic dissection in a mouse model of Marfan syndrome
Q53462382	Paraesophageal hernia: a rare presentation of Marfan syndrome in adults.
Q50100906	Paranoid schizophrenia in a woman with Marfan syndrome.
Q70480654	Parental age effects on the occurrence of new mutations for the Marfan syndrome
Q100506909	Parenting a child with Marfan syndrome: Distress and everyday problems
Q52064566	Partial characterization of an unusual 185 kDa protein synthesized by dermal fibroblasts from patients with Marfan syndrome: identification of the protein as type IV collagen.
Q64288453	Partial outflow pump dehiscence following off-pump HeartWare left ventricular assist device implantation in a patient with the Marfan syndrome
Q59054296	Partial sequence of a candidate gene for the Marfan syndrome
Q89403826	Participation of oleic acid in the formation of the aortic aneurysm in Marfan syndrome patients
Q44335774	Paternal fibrillin-1 mutation transmitted to an affected son with neonatal marfan syndrome: the importance of early recognition
Q56988733	Pathogenic FBN1 mutations in 146 adults not meeting clinical diagnostic criteria for Marfan syndrome: Further delineation of type 1 fibrillinopathies and focus on patients with an isolated major criterion
Q74313297	Pathology teach and tell: neonatal Marfan syndrome
Q88084654	Pathophysiology and Japanese clinical characteristics in Marfan syndrome
Q54646261	Patient with Marfan Syndrome and a Novel Variant in FBN1 Presenting with Bilateral Popliteal Artery Aneurysm.
Q43629808	Pediatric patients with Marfan syndrome: frequency of dural ectasia and its correlation with common cardiovascular manifestations
Q38630886	Penetration of left and right atrial wall and aortic root by an Amplatzer atrial septal occluder in a nine year old boy with Marfan syndrome: Case report.
Q90932687	Perinatal and cardiovascular outcomes in a pregnant patient with Marfan syndrome
Q91085256	Perinatal diagnosis and management of early-onset Marfan syndrome: case report and systematic review
Q64039354	Periodontal condition in growing subjects with Marfan Syndrome: a case-control study
Q21254709	Periodontal conditions in patients with Marfan syndrome - a multicenter case control study
Q47750463	Periodontitis May Deteriorate Sinus of Valsalva Dilatation in Marfan Syndrome Patients
Q39158416	Peripartum type B aortic dissection in patients with Marfan syndrome who underwent aortic root replacement: a case series study
Q54963245	Personal resources and satisfaction with life in Marfan syndrome patients with aortic pathology and in abdominal aortic aneurysm patients.
Q33659622	Personalised external aortic root support (PEARS) in Marfan syndrome: analysis of 1-9 year outcomes by intention-to-treat in a cohort of the first 30 consecutive patients to receive a novel tissue and valve-conserving procedure, compared with the pu
Q26864278	Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome
Q93128118	Pharmacotherapeutics for prevention of aortic root enlargement in Marfan Syndrome - A network meta-analysis of randomized controlled trials
Q73348165	Phenotypic alteration of vascular smooth muscle cells precedes elastolysis in a mouse model of Marfan syndrome
Q84759612	Phenotypic variability in Marfan syndrome in a family with a novel nonsense FBN1 gene mutation
Q80976824	Picture of the month: Marfan syndrome
Q90077667	Pigment dispersion syndrome and response to laser peripheral iridotomies in a child with Marfan syndrome
Q79233195	Plain radiography of the lumbosacral spine in Marfan syndrome
Q101217492	Pleural changes in patients with pneumothoraces and Marfan syndrome
Q85948342	Pneumatic retinopexy for primary repair of rhegmatogenous retinal detachment in marfan syndrome
Q34267639	Pneumothorax in the Marfan syndrome: prevalence and therapy
Q77734741	Point of view: Marfan syndrome: be aware of life-threatening complications
Q40566689	Polycystic kidneys associated with Marfan syndrome in an adult
Q74170034	Popliteal pterygium associated with neonatal Marfan syndrome: case report
Q87349266	Postmortem diagnosis of Marfan syndrome in a case of sudden death due to aortic rupture: Detection of a novel FBN1 frameshift mutation
Q84783517	Postmortem genetic analysis for a sudden death case complicated with Marfan syndrome
Q87187758	Postpartum type B aortic dissection in Marfan syndrome
Q91211813	Postural control abnormalities related to sleep deprivation in patients with Marfan Syndrome
Q36081849	Postural headache in a child with Marfan syndrome: case report and review of the literature
Q39291444	Postural headache in marfan syndrome associated with spinal cysts and liquor hypotension
Q87165340	Potential Phenotype-Genotype Correlation in Marfan Syndrome: When Less is More?
Q64044141	Precise Therapy for Thoracic Aortic Aneurysm in Marfan Syndrome: A Puzzle Nearing Its Solution
Q57210018	Predictors of Rapid Aortic Root Dilation and Referral for Aortic Surgery in Marfan Syndrome
Q81341270	Pregnancy and aortic root growth in the Marfan syndrome: a prospective study
Q84567864	Pregnancy and marfan syndrome: an ongoing discussion
Q88014318	Pregnancy and mesenchimal dysplasias (Marfan syndrome, Ehlers-Danlos syndrome, hereditary hemorrhagic telangiectasia)
Q37123586	Pregnancy in Marfan syndrome after aortic root replacement: a case report and review of the literature
Q37614886	Pregnancy in Marfan syndrome: maternal and fetal risk and recommendations for patient assessment and management
Q46316266	Pregnancy outcomes in Marfan syndrome: a retrospective cohort study
Q88285425	Pregnancy, Marfan syndrome, and type-B aortic dissection
Q39216614	Pregnancy-related acute aortic dissection in Marfan syndrome: A review of the literature.
Q73258423	Preimplantation genetic diagnosis in Marfan syndrome
Q54577590	Preimplantation genetic diagnosis of Marfan syndrome using multiple displacement amplification.
Q31915229	Preimplantation genetic diagnosis of Marfan syndrome with the use of fluorescent polymerase chain reaction and the Automated Laser Fluorescence DNA Sequencer.
Q91906771	Preliminary analysis of the association of TRPV1 to the formation of Marfan syndrome aneurysms
Q36496901	Prenatal Marfan syndrome: report of one case and review of the literature
Q74778405	Prenatal and presymptomatic diagnosis of Marfan syndrome using fluorescence PCR and an automated sequencer
Q72022436	Prenatal and presymptomatic diagnosis of the Marfan syndrome using fluorescence PCR and an automated sequencer
Q89229432	Prenatal care and labor in patients with mesenchimal dysplasias (Marfan syndrome, Ehlers-Danlos syndrome, hereditary hemorrhagic telangiectasia)
Q80423914	Prenatal diagnosis of Marfan syndrome
Q92269892	Prenatal diagnosis of Marfan syndrome by fetal echocardiography: A case report and review of cardiovascular manifestations
Q71375802	Prenatal diagnosis of Marfan syndrome: identification of a fibrillin-1 mutation in chorionic villus sample
Q83731002	Prenatal diagnosis of neonatal Marfan syndrome
Q68874399	Preoperative magnetic resonance imaging in Marfan syndrome
Q89836511	Presentation, surgical intervention, and long-term survival in patients with Marfan syndrome
Q33419013	Prevalence data on all Ghent features in a cross-sectional study of 87 adults with proven Marfan syndrome
Q91177649	Prevalence of Functional GI Diseases and Pelvic Floor Symptoms in Marfan Syndrome and Ehlers-Danlos Syndrome: A National Cohort Study
Q49144858	Prevalence of dural ectasia in 63 gene-mutation-positive patients with features of Marfan syndrome type 1 and Loeys-Dietz syndrome and report of 22 novel FBN1 mutations.
Q35005489	Prevalence of dural ectasia in Loeys-Dietz syndrome: comparison with Marfan syndrome and normal controls
Q61631832	Prevalence of pulp calcifications in patients with Marfan syndrome
Q92302098	Prevalence of temporal bone tegmen defects among patients with Marfan syndrome
Q84707828	Preventative valve-sparing aortic root replacement and pregnancy outcome in Marfan syndrome
Q35120570	Preventing the aortic complications of Marfan syndrome: a case-example of translational genomic medicine
Q102319389	Preventive surgery in Marfan syndrome: which one is appropriate?
Q104286567	Primary cardiac impairment in patients with Marfan syndrome undergoing a Bentall procedure
Q61797449	Primary midgut volvulus in a patient with Marfan syndrome
Q87900145	Primary spontaneous pneumothorax in conjunction with Marfan syndrome
Q80360604	Primary trabeculodysgenesis in association with neonatal Marfan syndrome
Q80159597	Primary versus secondary intraocular lens placement after pars plana lensectomy in pediatric Marfan syndrome
Q68428386	Probable Homozygotic Form of the Marfan Syndrome in a Newborn Child
Q72252092	Problems and management of surgery on aorta and heart in Marfan syndrome
Q57222960	Prognostic significance of the pattern of aortic root dilation in the Marfan syndrome
Q91097321	Progressive Pulmonary Artery Dilatation is Associated with Type B Aortic Dissection in Patients with Marfan Syndrome
Q43492641	Progressive cardiomyopathic lentiginosis (LEOPARD syndrome) in 3 patients, combined with Marfan syndrome
Q92935146	Progressive double major scoliotic curve with concurrent lumbosacral spondylolisthesis in a skeletally immature patient with Marfan syndrome treated with anterior scoliosis correction
Q49161938	Prophylactic aortic root surgery in patients with Marfan syndrome: 10 years' experience with a protocol based on body surface area.
Q39158663	Prophylactiv use of propranolol in the Marfan syndrome to prevent aortic dissection
Q84500105	Proteomic analysis in aortic media of patients with Marfan syndrome reveals increased activity of calpain 2 in aortic aneurysms
Q73829806	Protrusio acetabuli and bilateral basicervical femoral neck fractures in a patient with Marfan syndrome
Q85047055	Protrusio acetabuli and total hip arthroplasty in patients with Marfan syndrome
Q43752616	Protrusio acetabuli in Marfan syndrome: age-related prevalence and associated hip function
Q36274782	Protrusio acetabuli in Marfan syndrome: indication for surgery in skeletally immature Marfan patients
Q41201312	Protrusio acetabuli: its occurrence in the completely expressed Marfan syndrome and its musculoskeletal component and a procedure to arrest the course of protrusion in the growing pelvis
Q93052828	Proximal aorta longitudinal strain predicts aortic root dilation rate and aortic events in Marfan syndrome
Q83842184	Proximal aortic perforation after endovascular repair of a type B dissection in a patient with Marfan syndrome
Q90136037	Pseudoaneurysm of the popliteal artery after hardware removal in a patient with Marfan syndrome
Q84168662	Pseudomeningocele induced transient loss of consciousness in Marfan syndrome
Q66953663	Pseudoxanthoma elasticum associated with Marfan syndrome (author's transl)
Q38622823	Psychiatric and neuropsychological issues in Marfan syndrome: A critical review of the literature.
Q98579541	Psychological factors affecting Marfan syndrome patients with or without cardiac surgery
Q33680704	Psychosocial adaptation in adolescents and young adults with Marfan syndrome: an exploratory study
Q35579953	Pulmonary artery root dilatation in Marfan syndrome: quantitative assessment of an unknown criterion
Q68612496	Pulmonary bullous disease in Marfan syndrome
Q68299329	Pulmonary emphysema in a neonate with Marfan syndrome
Q69648773	Pulmonary emphysema in a neonate with Marfan syndrome
Q68261781	Pulmonary emphysema in neonate with the Marfan syndrome
Q69748145	Pulmonary function in the Marfan syndrome
Q34233749	Pulmonary histologic changes in Marfan syndrome: a case series and literature review
Q69242409	Pulmonary hyperinflation and emphysema in infants with the Marfan syndrome
Q36077929	Pulmonary involvement in collagen vascular disease: a review of the pulmonary manifestations of the Marfan syndrome, ankylosing spondylitis, Sjögren's syndrome, and relapsing polychondritis
Q64043840	Pulmonary venous obstruction in a patient with Marfan syndrome: Rare presentation of an expanding dissecting descending thoracic aortic aneurysm with annuloaortic ectasia
Q48237118	Pupillary manifestations of Marfan syndrome: from the Marfan eye consortium of Chicago.
Q80769480	Quadrivalvar replacement in infantile Marfan syndrome
Q93116233	Quality of Life of Patients With Marfan Syndrome After Valve-Sparing or Valve-Replacement Operations
Q51062254	Quantification of aortic and cutaneous elastin and collagen morphology in Marfan syndrome by multiphoton microscopy.
Q95657202	Quantifying the Genetic Basis of Marfan Syndrome Clinical Variability
Q71956165	Quantitation of fibrillin immunofluorescence in fibroblast cultures in the Marfan syndrome
Q74285941	Quantitative assessment of dural ectasia as a marker for Marfan syndrome
Q34234444	Quantitative differences in biosynthesis and extracellular deposition of fibrillin in cultured fibroblasts distinguish five groups of Marfan syndrome patients and suggest distinct pathogenetic mechanisms
Q102369222	Quantitative proteomics reveal lineage-specific protein profiles in iPSC-derived Marfan syndrome smooth muscle cells
Q84825348	Radicular dysfunction due to spinal deformities in Marfan syndrome at older age: three case reports
Q81535386	Radiofrequency ablation of a left-sided atrioventricular pathway in a patient with Marfan syndrome
Q49043658	Radiotherapy and Marfan syndrome: a report of two cases.
Q30476899	Rationale and design of a randomized clinical trial of beta-blocker therapy (atenolol) versus angiotensin II receptor blocker therapy (losartan) in individuals with Marfan syndrome
Q34980288	Rationale and design of a trial evaluating the effects of losartan vs. nebivolol vs. the association of both on the progression of aortic root dilation in Marfan syndrome with FBN1 gene mutations
Q88728308	Re: Peripartum type B aortic dissection in patients with Marfan syndrome who underwent aortic root replacement: a case series study
Q33717760	Recapitulating and Correcting Marfan Syndrome in a Cellular Model
Q38685185	Recent Clinical Drug Trials Evidence in Marfan Syndrome and Clinical Implications
Q37074616	Recent advances in understanding Marfan syndrome: should we now treat surgical patients with losartan?
Q85346086	Recent developments in the diagnosis of Marfan syndrome and related disorders
Q37601641	Recent molecular biological progress in Marfan syndrome and Marfan-associated disorders
Q36633070	Recent progress in genetics of Marfan syndrome and Marfan-associated disorders
Q67916593	Recessive autosomal inheritance in Marfan syndrome
Q34389307	Recurrence of Marfan syndrome as a result of parental germ-line mosaicism for an FBN1 mutation
Q33688200	Recurrent and founder mutations in the Netherlands: Extensive clinical variability in Marfan syndrome patients with a single novel recurrent fibrillin-1 missense mutation
Q89082380	Redo Aortic Root Operations in Patients with Marfan Syndrome
Q92203641	Redo aortic root replacement for postoperative left ventricular outflow tract pseudoaneurysm after valve-sparing aortic root replacement in a patient with Marfan syndrome
Q51748830	Redox stress in Marfan syndrome: Dissecting the role of the NADPH oxidase NOX4 in aortic aneurysm.
Q69584219	Reduced activity of serum beta-glucuronidase in Marfan syndrome
Q64249766	Reference Expression Profile of Three Transcript Isoforms and Their Association with Clinical Variability in Marfan Syndrome
Q48131167	Regional anesthesia in Marfan syndrome, not all dural ectasias are the same: a report of two cases
Q85343852	Regional changes in elastic fiber organization and transforming growth factor β signaling in aortas from a mouse model of marfan syndrome
Q53970190	Reimplantation for Marfan syndrome: If it ain't broke….
Q36720004	Reimplantation valve-sparing aortic root replacement in Marfan syndrome using the Valsalva conduit: an intercontinental multicenter study
Q43491016	Relapse of Escherichia coli meningitidis due to sacral meningocele in Marfan syndrome, treated only with antibiotherapy
Q59250390	Relation between age and aortic wall compliance in the Marfan syndrome: evaluation with Velocity-Encoded MRI
Q59095941	Relation between genotype and left-ventricular dilatation in patients with Marfan syndrome
Q45187276	Relationship between finger length and ridge count in patients with Marfan syndrome
Q70590284	Renal Arteriovenous Fistula: Unique Finding in the Marfan Syndrome
Q71343710	Renal disease in Marfan syndrome
Q73594156	Renovascular hypertension in Marfan syndrome
Q84586307	Reoperation for ascending aorta and total arch replacement combined with patent ductus arteriosus closure in a child with marfan syndrome
Q35662017	Repair of a ruptured sinus of Valsalva aneurysm. Associated with annuloaortic ectasia and coarctation of the aorta in a patient with Marfan syndrome
Q82790926	Repair of the entire aorta and heart valves in a patient with Marfan syndrome
Q73280374	Replacement of the aortic root in patients with Marfan syndrome
Q89155961	Reply to "Aortic repair in Marfan Syndrome: Let's not forget the arch when talking about the root"
Q35533403	Report of a Japanese girl with Marfan syndrome associated with insulin-dependent diabetes mellitus
Q34017755	Report of the National Heart, Lung, and Blood Institute and National Marfan Foundation Working Group on research in Marfan syndrome and related disorders
Q26774737	Republished review: Surgical management of aortic root disease in Marfan syndrome and other congenital disorders associated with aortic root aneurysms
Q38671673	Republished: Marfan syndrome, inherited aortopathies and exercise: What is the right answer?
Q57021693	Rescue Nuss procedure for inferior vena cava compression syndrome following posterior scoliosis surgery in Marfan syndrome
Q80512792	Respiratory dysfunction in patients with Marfan syndrome
Q60637233	Response to letter by Mkrtchyan regarding article: “Aortic biomechanics by magnetic resonance: Early markers of aortic disease in Marfan syndrome regardless of aortic dilatation?”
Q87274296	Results after thoracic aortic reoperations in Marfan syndrome
Q38410285	Results of Open Surgical Repair in Patients With Marfan Syndrome and Distal Aortic Dissection
Q81326858	Results of aortic surgery in patients with Marfan syndrome
Q72015447	Results of pulmonary function testing in 5 persons with the Marfan syndrome
Q75225483	Results of retinal detachment surgery in Marfan syndrome in Asians
Q35090447	Results of retinal detachment surgery in Marfan syndrome in asians
Q91892599	Results of staged repair of aortic disease in patients with Marfan syndrome
Q61648589	Results of surgery for aortic root aneurysm in patients with Marfan syndrome
Q35808304	Retinal Disease in Marfan Syndrome: From the Marfan Eye Consortium of Chicago
Q98907353	Retinal and Choroidal Vasculature in Patients with Marfan Syndrome
Q74195939	Retinal detachment in Marfan syndrome
Q44097533	Retinal detachment in Marfan syndrome: clinical characteristics and surgical outcome
Q82735789	Retreatment of a patient with Marfan syndrome and severe root resorption
Q84579098	Retrograde endovascular treatment of internal iliac aneurysm in a patient with Marfan syndrome
Q84475072	Reverse chimney or periscope: some issues have to be addressed "Re: Endovascular aneurysm repair using a reverse chimney technique in a patient with Marfan syndrome and contained ruptured chronic type B dissection"
Q39562230	Revised Ghent Criteria is Comparable to Original Diagnostic Criteria for Marfan Syndrome with Increased Ability to Clinically Diagnose Related Disorders
Q84993401	Revised diagnostic criteria for Marfan syndrome
Q56874464	Revised diagnostic criteria for the Marfan syndrome
Q82944647	Revised diagnostic criteria for the marfan syndrome a clinical-radiographic essay
Q104740034	Risk Factors and Inadequacy of Screening for Sleep-Disordered Breathing in Children with Marfan Syndrome
Q85069141	Role of angiotensin receptor blockers for management of aortic root dilation associated with Marfan syndrome
Q91508154	Role of losartan in prevention of aortic dilatation in Marfan syndrome: A systematic review and meta-analysis
Q90855171	Rupture of Giant Anterior Sacral Meningocele in a Patient with Marfan Syndrome: Diagnosis and Management
Q92761042	Rupture of a Type B Aortic Dissection in a Postpartum Patient with Marfan Syndrome
Q83294809	Rupture of chronic thoracic aortic dissection in a Marfan syndrome patient after heart transplantation
Q55174921	Ruptured abdominal aortic aneurysm repair in pediatric Marfan syndrome patient.
Q84489312	Ruptured thoracoabdominal aneurysm with aortocaval fistula, aortic dissection type III, and bilateral femoral aneurysms in patient with Marfan syndrome
Q76623301	SKELETAL MANIFESTATIONS IN THE MARFAN SYNDROME
Q99399900	STABILISE technique for a non-A non-B acute aortic dissection in Marfan syndrome
Q72792547	Sacral Abnormalities in Marfan Syndrome
Q86775949	Sacral erosion and insufficiency fracture secondary to dural ectasia in patient with Marfan syndrome
Q56796515	Safety and cardiovascular behavior during pulmonary function in patients with Marfan syndrome
Q37131093	Sagittal balance in scoliosis associated with Marfan syndrome: a stereoradiographic three-dimensional analysis
Q47866323	Satisfaction with life in adults with Marfan syndrome (MFS): associations with health-related consequences of MFS, pain, fatigue, and demographic factors
Q91329189	Schizophrenia in a Man With Probable Marfan Syndrome
Q51806787	Screening for aortic root dilation in marfan syndrome using the ratio of the aortic root to descending aortic diameters in children.
Q80702024	Search for correlations between FBN1 genotype and complete Ghent phenotype in 44 unrelated Norwegian patients with Marfan syndrome
Q72223749	Second international symposium on the Marfan syndrome, November 7-9, 1992, San Francisco, CA
Q72532979	Sensitive detection of abnormal aortic architecture in Marfan syndrome with high-frequency ultrasonic tissue characterization
Q35438154	Sensitivity of conformation sensitive gel electrophoresis in detecting mutations in Marfan syndrome and related conditions
Q100495939	Separation in genetic pathogenesis of mutations in FBN1-TB5 region between autosomal dominant acromelic dysplasia and Marfan syndrome
Q79141569	Serum seromucoid and acid mucopolysaccharide in the Marfan syndrome
Q78979919	Serum seromucoid levels in the Marfan syndrome
Q81083804	Severe Marfan syndrome due to FBN1 exon deletions
Q90962267	Severe aortic root dilatation in infantile Marfan syndrome
Q80971155	Severe cardiovascular features of marfan syndrome in childhood: just another manifestation or a specific entity?
Q81346778	Severe infantile Marfan syndrome versus neonatal Marfan syndrome
Q35889026	Severe neonatal Marfan syndrome resulting from a de novo 3-bp insertion into the fibrillin gene on chromosome 15.
Q47860104	Severe spontaneous intracranial hypotension and Marfan syndrome in an adolescent
Q47204149	Shortening of growing-rod spinal instrumentation reverses cardiac failure in child with Marfan syndrome and scoliosis. A case report
Q38002417	Should we prescribe "vasodilating" beta-blockers in Marfan syndrome to prevent aortic aneurysm and dissection?
Q38985630	Shprintzen-Goldberg syndrome: a rare disorder
Q73552939	Silent mutation induces exon skipping of fibrillin-1 gene in Marfan syndrome
Q71081928	Simultaneous Bentall's procedure and sternal turnover in a patient with Marfan syndrome
Q83206023	Simultaneous repair for aortic incompetence with annuloaortic ectasia and pectus excavatum by modified Ravitch procedure with pectus bars in an adult patient with Marfan syndrome
Q97651657	Single-Cell Transcriptomic Profiling of Vascular Smooth Muscle Cell Phenotype Modulation in Marfan Syndrome Aortic Aneurysm
Q73143563	Six novel mutations of the fibrillin-1 gene in Korean patients with Marfan syndrome
Q40068025	Skeletal evolution in Marfan syndrome: Growth curves from French national cohort
Q28077286	Skeletal manifestations of Marfan syndrome associated to heterozygous R2726W FBN1 variant: sibling case report and literature review
Q93069265	Sleep apnea and the impact on cardiovascular risk in patients with Marfan syndrome
Q91213295	Sleep disordered breathing in Marfan syndrome: Value of standard screening questionnaires
Q64277451	Soluble EMMPRIN levels discriminate aortic ectasia in Marfan syndrome patients
Q27732794	Solution structure of a pair of calcium-binding epidermal growth factor-like domains: implications for the Marfan syndrome and other genetic disorders
Q44167101	Sounding the alarm. If undetected, Marfan syndrome can be a silent killer.
Q66978635	Special surgical problems related to aortic dissections in the Marfan syndrome: complete replacement of the ascending aorta and the aortic valve with reimplantation of coronary arteries (author's transl)
Q99604936	Specific miRNA and Gene Deregulation Characterize the Increased Angiogenic Remodeling of Thoracic Aneurysmatic Aortopathy in Marfan Syndrome
Q48009345	Spinal deformity correction in Marfan syndrome versus adolescent idiopathic scoliosis: learning from the differences
Q100737689	Spinal fusion in pediatric patients with marfan syndrome: a nationwide assessment on short-term outcomes and readmission risk
Q87193137	Spinal imaging features in Japanese patients with Marfan syndrome: a case-control study
Q91702709	Spinal meningeal cyst in a child with Marfan syndrome: A potential cause for apparent dural puncture during caudal epidural block
Q53765268	Spleen rupture after surgery in Marfan syndrome scoliosis.
Q47861010	Splicing mutation in the fibrillin-1 gene associated with neonatal Marfan syndrome and severe pulmonary emphysema with tracheobronchomalacia
Q96958340	Spontaneous Multilevel Cerebrospinal Fluid Leak in Marfan Syndrome
Q71016437	Spontaneous Pneumothorax in a Patient with Marfan Syndrome
Q100312834	Spontaneous Right Ventricular Pseudoaneurysms and Increased Arrhythmogenicity in a Mouse Model of Marfan Syndrome
Q70678281	Spontaneous dissecting aneurysm of the ductus arteriosus in an infant with Marfan syndrome
Q33618489	Spontaneous dural tear leading to intracranial hypotension and tonsillar herniation in Marfan syndrome: a case report
Q80490721	Spontaneous intracranial hypotension syndrome in a patient with marfan syndrome and autosomal dominant polycystic kidney disease
Q34117417	Spontaneous spinal cerebrospinal fluid leaks and minor skeletal features of Marfan syndrome: a microfibrillopathy
Q82569768	Sports and marfan syndrome: awareness and early diagnosis can prevent sudden death
Q89476914	Staged hybrid aortic procedure for chronic type B aortic dissection in two patients with Marfan syndrome
Q36582103	Stanford type A aortic dissection in a patient with Marfan syndrome during pregnancy: a case report.
Q64917008	Statins Reduce Thoracic Aortic Aneurysm Growth in Marfan Syndrome Mice via Inhibition of the Ras-Induced ERK (Extracellular Signal-Regulated Kinase) Signaling Pathway.
Q100504026	Steered molecular dynamic simulations reveal Marfan syndrome mutations disrupt fibrillin-1 cbEGF domain mechanosensitive calcium binding
Q73582756	Stent graft placement of the thoracoabdominal aorta in a patient with Marfan syndrome
Q51621880	Stent graft repair of descending aortic dissection in patients with Marfan syndrome: an effective alternative to open reoperation?
Q91455811	Stent use in patients with Marfan syndrome: Not so crazy after all
Q89204335	Stent-assisted, balloon-induced intimal disruption and relamination of aortic dissection in patients with Marfan syndrome: Midterm outcomes and aortic remodeling
Q72395574	Strabismus in the Marfan syndrome
Q49052413	Strategies for prenatal and preimplantation genetic diagnosis in Marfan syndrome (MFS).
Q70210659	Studies on elastic tissue of aorta in aortic dissections and Marfan syndrome
Q43823169	Study of phenotype evolution during childhood in Marfan syndrome to improve clinical recognition.
Q84289623	Subclavian artery aneurysm in Marfan syndrome
Q104694229	Subclavian artery aneurysmal rupture and left internal mammary artery extravasation secondary to advanced Marfan syndrome
Q96439337	Sublaminar fixation versus hooks and pedicle screws in scoliosis surgery for Marfan syndrome
Q38307738	Substitution of a cysteine residue in a non-calcium binding, EGF-like domain of fibrillin segregates with the Marfan syndrome in a large kindred
Q91120407	Successful Thrombolysis in the Setting of Marfan Syndrome and Chronic Aortic Dissection
Q84155905	Successful aortic reimplantation in a three-year-old child with Marfan syndrome
Q43184222	Successful management of a patient with Marfan syndrome complicated with acute aortic dissection using landiolol during Cesarean section.
Q44050441	Successful management of aortic dissection in a patient with Marfan syndrome during pregnancy
Q43412043	Successful management of aortic dissection in a patient with Marfan syndrome with total placenta previa
Q92982193	Successful orthotopic heart transplantation in a patient with Marfan syndrome
Q90981355	Successful repair of a popliteal aneurysm with saphenous vein graft in a patient with Marfan syndrome
Q90642214	Successful spinal anaesthesia for caesarean section in a patient with Marfan syndrome complicated by dural ectasia
Q74805152	Successful treatment in a patient with Takayasu's arteritis and Marfan syndrome
Q79317837	Sudden death due to atlantoaxial subluxation in marfan syndrome
Q72324098	Sudden death in Marfan syndrome
Q87243935	Sudden death in Marfan syndrome
Q87844303	Superficial Siderosis and Dural Ectasia in a Patient with Marfan Syndrome
Q30895539	Suprachoroidal hemorrhage during silicone oil removal in Marfan syndrome
Q38698419	Surgery for patients with Marfan syndrome with type A dissection involving the aortic arch using total arch replacement combined with stented elephant trunk implantation: the acute versus the chronic
Q82075484	Surgery for type A aortic dissection in pregnant patients with Marfan syndrome
Q35099493	Surgical Management of Mitral Regurgitation in Patients with Marfan Syndrome during Infancy and Early Childhood
Q91126686	Surgical Management of Type A Acute Aortic Dissection in Patients With Marfan Syndrome: A Single Center Experience
Q49679196	Surgical Treatment of Anterior Sacral Meningoceles in Patients with Marfan Syndrome: A Report of Three Cases.
Q55101882	Surgical Treatment of a Left Axillary Arterial Aneurysm with Marfan Syndrome by Combining Two Skin Incisions.
Q41790646	Surgical approach for Stanford type A aortic dissection in a patient with Marfan syndrome and pectus excavatum
Q84218977	Surgical approach to left subclavian artery aneurysm in Marfan syndrome
Q72341736	Surgical management of Marfan syndrome in children
Q38225495	Surgical management of aortic root disease in Marfan syndrome and other congenital disorders associated with aortic root aneurysms.
Q33791762	Surgical management of aortic root disease in Marfan syndrome: a systematic review and meta-analysis
Q68050074	Surgical management of children and young adults with Marfan syndrome and pectus excavatum
Q49030183	Surgical management of patients with Marfan syndrome: evolution throughout the years.
Q71445189	Surgical management of patients with the Marfan syndrome and dilatation of the ascending aorta
Q35585628	Surgical reconstruction of aortic root in Marfan syndrome patients: a systematic review
Q38702674	Surgical results for aortic involvement in Marfan syndrome
Q88790012	Surgical treatment of Marfan syndrome and related disorders is all about dealing with uncertainties
Q38702670	Surgical treatment of Marfan syndrome; analysis of the patients required multiple surgical interventions
Q54134157	Surgical treatment of aortic root aneurysm related to Marfan syndrome in early childhood.
Q51690112	Surgical treatment of ascending aortic complications in Marfan syndrome: early and long-term outcomes.
Q43546151	Surgical treatment of cardiovascular complications in Marfan syndrome: a 27-year experience
Q38027169	Surgical treatment of cardiovascular complications in patients with Marfan syndrome: a report of two cases and literature review.
Q43947000	Surgical treatment of dislocated lenses in the Marfan syndrome and homocystinuria
Q82509299	Surgical treatment of scoliosis associated with Marfan syndrome by using posterior-only instrumentation
Q77965383	Surgical treatment of scoliosis in Marfan syndrome: guidelines for a successful outcome
Q40688915	Surgical treatment of scoliosis in Marfan syndrome: outcomes and complications
Q91474882	Surgical treatment of spinal deformities in Marfan syndrome: Long-term follow-up results using different instrumentations
Q58613135	Survival, causes of death, and cardiovascular events in patients with Marfan syndrome
Q46000642	Suspected Marfan Syndrome in a Female Basketball Player.
Q43507548	Symposium on the musculoskeletal aspects of Marfan syndrome: meeting report and state of the science
Q78811484	Symptomatic enlarged cervical anterior epidural venous plexus in a patient with Marfan syndrome
Q94167451	Symptomatic enlarged cervical anterior epidural venous plexus in a patient with Marfan syndrome
Q57972059	Symptomatic valvular myxomatous transformation (the floppy valve syndrome). A possible forme fruste of the Marfan syndrome
Q91851969	TEVAR in Patients With Marfan Syndrome: From Bailout to Strategy
Q92419010	TGF-β mediates aortic smooth muscle cell senescence in Marfan syndrome
Q49080920	TGFBR1 and TGFBR2 mutations in patients with features of Marfan syndrome and Loeys-Dietz syndrome.
Q47885926	TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies
Q78397806	THE MARFAN SYNDROME AND PREGNANCY
Q46398783	THE MARFAN SYNDROME AND PREGNANCY.
Q76715893	THE MARFAN SYNDROME: GIGANTISM AND RUPTURED ABDOMINAL ANEURYSM
Q76618769	THE NATURE OF THE CONNECTIVE TISSUE ABIOTROPHY IN THE MARFAN SYNDROME
Q89013037	Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Guidelines for the Interpretation of Sequenced Variants in the FBN1 Gene for Marfan Syndrome: Proposal for a Disease- and Gene-Specific Guide
Q61809010	Targeted deletion of fibrillin-1 in the mouse eye results in ectopia lentis and other ocular phenotypes associated with Marfan syndrome
Q86125338	Targeting transforming growth factor-β signaling in aortopathies in Marfan syndrome
Q30276267	Teaching NeuroImages: Intracranial hypotension in a patient with Marfan syndrome
Q80111647	Temporomandibular joint dysfunction in Marfan syndrome
Q91802674	Ten-year reinvestigation of ocular manifestations in Marfan syndrome
Q57150264	The 8th international research symposium on the Marfan Syndrome and related conditions
Q36418768	The Beneficial Effect of Renin-Angiotensin-Aldosterone System Blockade in Marfan Syndrome Patients after Aortic Root Replacement.
Q30464944	The Ehlers-Danlos syndromes and Marfan syndrome: inherited diseases of connective tissue with overlapping clinical features
Q58729318	The Evaluation of Flow-Mediated Vasodilation in the Brachial Artery Correlates With Endothelial Dysfunction Evaluated by Nitric Oxide Synthase Metabolites in Marfan Syndrome Patients
Q54655441	The Human Genome Project and clinical medicine: adenomatous polyposis coli and the Marfan syndrome as examples.
Q39196126	The Incidence and Severity of Physical Pain Symptoms in Marfan Syndrome: A Survey of 993 Patients
Q102385841	The Late Effects of Pregnancy on Aortic Dimensions in Patients with Marfan Syndrome
Q67010299	The Marfan Syndrome, Coarctation of the Aorta, and Precocious Puberty
Q70919598	The Marfan Syndrome: A Deficiency in Chemically Stable Collagen Cross-Links
Q39788812	The Marfan Syndrome: Diagnosis and Management
Q58748550	The Marfan syndrome
Q69680545	The Marfan syndrome
Q70894157	The Marfan syndrome
Q74612258	The Marfan syndrome
Q74734063	The Marfan syndrome
Q79474524	The Marfan syndrome
Q81314277	The Marfan syndrome
Q34187732	The Marfan syndrome - features, natural history and treatment options - our experiences.
Q67319843	The Marfan syndrome and cardiac surgery
Q67750833	The Marfan syndrome and pregnancy
Q74410337	The Marfan syndrome and pregnancy: a retrospective study in a Dutch population
Q34988927	The Marfan syndrome and related connective tissue disorders
Q41005075	The Marfan syndrome and the cardiovascular surgeon
Q78888899	The Marfan syndrome associated with an unusual interventricular septal defect
Q43646117	The Marfan syndrome gene is localized
Q72145431	The Marfan syndrome gene locus as a favoured locus for susceptibility to schizophrenia
Q71782859	The Marfan syndrome in early childhood: analysis of 15 patients diagnosed at less than 4 years of age
Q44643197	The Marfan syndrome in pregnancy: A case report
Q71707371	The Marfan syndrome in pregnancy: a case report
Q68094152	The Marfan syndrome is caused by a point mutation in the fibrillin gene
Q70118986	The Marfan syndrome locus: confirmation of assignment to chromosome 15 and identification of tightly linked markers at 15q15-q21.3.
Q69946167	The Marfan syndrome revisited
Q68351074	The Marfan syndrome with an XYY chromosome pattern
Q78371551	The Marfan syndrome, with special reference to congenital enlargement of the spinal canal
Q70190054	The Marfan syndrome: abnormal aortic elastic properties
Q68063168	The Marfan syndrome: cardiovascular physical findings and diagnostic correlates
Q79636924	The Marfan syndrome: case report of the incomplete form (forme fruste)
Q37617524	The Marfan syndrome: implications for athletes and their echocardiographic assessment
Q39378297	The Marfan syndrome: joint and skin manifestations are prevalent and correlated
Q72939545	The Marfan syndrome: report of an interesting case with unusual anatomic findings
Q35272315	The Marfan syndrome: report of one case with autopsy, special histological study, and review of the literature
Q71204900	The Marfan syndrome: surgical technique and follow-up in 50 patients
Q74526278	The Marfan syndrome; a report of an atypical case
Q64063306	The Potential Beneficial Effects of Resveratrol on Cardiovascular Complications in Marfan Syndrome Patients⁻Insights from Rodent-Based Animal Studies
Q37677706	The Prevalence of Marfan Syndrome in Korea
Q88477689	The Pulmonary Artery in Pediatric Patients with Marfan Syndrome: An Underestimated Aspect of the Disease
Q68419536	The accumulation of hyaluronic acid in cultured fibroblasts of the Marfan syndrome
Q73152416	The association of absent suspensory ligaments of the liver and Marfan syndrome
Q28362710	The borohydride-reducible compounds of human aortic elastin. Demonstration of a new cyclic amino acid in alkali hydrolysate, and changes with age and in patients with annulo-aortic ectasia including one with Marfan syndrome
Q37183278	The characteristics of acute aortic dissection among young Chinese patients: a comparison between Marfan syndrome and non-Marfan syndrome patients
Q62870647	The clinical presentation of Marfan syndrome is modulated by expression of wild-type FBN1 allele
Q100389265	The corneoscleral shape in Marfan syndrome
Q98893338	The correlation between spinal and chest wall deformities and pulmonary function in Marfan syndrome
Q22122364	The defect in Marfan syndrome
Q99201639	The differences in surgical long-term outcomes between Marfan syndrome and Loeys-Dietz syndrome
Q33848798	The economic impact of Marfan syndrome: a non-experimental, retrospective, population-based matched cohort study
Q90023788	The effects of losartan versus beta-blockers on cardiovascular protection in marfan syndrome: A systematic review and meta-analysis
Q59096098	The expanding cardiovascular phenotype of Marfan syndrome
Q34211973	The eye in the Marfan syndrome
Q72118711	The eye in the Marfan syndrome
Q48143758	The face in marfan syndrome: A 3D quantitative approach for a better definition of dysmorphic features
Q46300455	The fibrillin-1 hypomorphic mgR/mgR murine model of Marfan syndrome shows severe elastolysis in all segments of the aorta.
Q47276925	The foot in Marfan syndrome: clinical findings and weight-distribution patterns.
Q33789095	The genetic basis of aortic disease. Marfan syndrome and beyond
Q37228790	The importance of genetic testing in the clinical management of patients with Marfan syndrome and related disorders
Q80686852	The importance of mutation detection in Marfan syndrome and Marfan-related disorders: report of 193 FBN1 mutations
Q91241032	The incidence of Marfan syndrome and cardiac anomalies in patients presenting with pectus deformities
Q31911942	The lumbar interpediculate distance is widened in adults with the Marfan syndrome: data from 32 cases
Q24656172	The molecular genetics of Marfan syndrome and related disorders
Q24681593	The molecular genetics of Marfan syndrome and related microfibrillopathies
Q49060891	The new Ghent criteria for Marfan syndrome: what do they change?
Q37738226	The pathogenesis of aortopathy in Marfan syndrome and related diseases
Q43568559	The pathogenicity of the Pro1148Ala substitution in the FBN1 gene: causing or predisposing to Marfan syndrome and aortic aneurysm, or clinically innocent?
Q98469670	The pattern and progression of hearing loss in Marfan Syndrome: A study of children and young adults
Q36846820	The phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome
Q84569496	The pulmonary artery in patients with Marfan syndrome: a cross-sectional study
Q72293571	The question of heterogeneity in Marfan syndrome
Q92710078	The reimplantation valve-sparing aortic root replacement technique for patients with Marfan syndrome: A single-center experience
Q28286547	The revised Ghent nosology for the Marfan syndrome
Q35044636	The revised role of TGF-β in aortic aneurysms in Marfan syndrome
Q28077230	The role of the multidisciplinary health care team in the management of patients with Marfan syndrome
Q44445930	The roles of two novel FBN1 gene mutations in the genotype-phenotype correlations of Marfan syndrome and ectopia lentis patients with marfanoid habitus
Q57149983	The search for genotype/phenotype correlation in Marfan syndrome: to be or not to be?
Q87805859	The spectrum of FBN1, TGFβR1, TGFβR2 and ACTA2 variants in 594 individuals with suspected Marfan Syndrome, Loeys-Dietz Syndrome or Thoracic Aortic Aneurysms and Dissections (TAAD)
Q40333407	The spectrum of cardiovascular disease in the Marfan syndrome: a clinico-morphologic study of 18 necropsy patients and comparison to 151 previously reported necropsy patients
Q56988740	The spectrum of syndromes and manifestations in individuals screened for suspected Marfan syndrome
Q48965268	The sudden arrival of Marfan syndrome: the Rust family's experience.
Q72315874	The thoracolumbar spine in Marfan syndrome
Q37395569	The unravelling of primary myocardial impairment in Marfan syndrome by modern echocardiography
Q38474851	The usefulness of multidetector computed tomographic angiography for the diagnosis of Marfan syndrome by Ghent criteria
Q68878393	The wrist sign in Marfan syndrome
Q34156835	Therapeutic management of patients with Marfan syndrome: focus on cardiovascular involvement
Q92985902	Thoracic Aortic, Aortic Valve, and Mitral Valve Surgery in Pediatric and Young Adult Patients With Marfan Syndrome: Characteristics and Outcomes
Q44705708	Thoracic cage deformities in the early diagnosis of the Marfan syndrome and cardiovascular disease
Q73383158	Thoracoabdominal aorta in Marfan syndrome: MR imaging findings of progression of vasculopathy after surgical repair
Q47102208	Thoracoabdominal aortic aneurysm repair in Marfan syndrome: how we do it.
Q80170018	Thoracoabdominal aortic aneurysm repair in patients with marfan syndrome
Q58764496	Thoracoscopic Treatment of Pneumothorax in Marfan Syndrome: Hemostatic Patch to Support Lung Resection Recovery
Q95283396	Three Novel Variants identified in FBN1 and TGFBR2 in seven Iranian families with suspected Marfan syndrome
Q73218531	Three novel fibrillin mutations in exons 25 and 27: classic versus neonatal Marfan syndrome
Q47279859	Three novel mutations of the fibrillin-1 gene and ten single nucleotide polymorphisms of the fibrillin-3 gene in Marfan syndrome patients
Q39413940	Three pregnancies in a Marfan syndrome patient after a mitral and tricuspid valve surgery.
Q90893779	Three-Dimensional Mitral Valve Morphology in Children and Young Adults With Marfan Syndrome
Q73593148	Three-channeled aortic dissection in Marfan syndrome
Q83815594	Three-dimensional analysis of the vertebral rotation associated with the lateral deviation in Marfan syndrome spinal deformity
Q93111039	Three-dimensional modeling of Marfan syndrome with elastic and hyperelastic materials assumptions using fluid-structure interaction
Q72121725	Three-staged graft replacement for multifocal aortic aneurysms in the Marfan syndrome
Q71713460	Thrombosis associated with a porcine bioprosthesis and ascending aortic graft in a patient with the Marfan syndrome
Q80902647	Timing of aortic surgery in the Marfan syndrome
Q45245044	Timing of the surgery in patients with Marfan syndrome and definition of the aortic aneurysm
Q83343226	Tissue Doppler imaging identifies myocardial dysfunction in adults with Marfan syndrome
Q56988753	Tissue Doppler imaging identifies myocardial dysfunction in adults with marfan syndrome
Q53314497	Total aortic repair in Marfan syndrome using stent grafting with hybrid techniques.
Q88077042	Total artificial heart implantation in a young Marfan syndrome patient
Q36319295	Total chordal augmentation in a child with Marfan syndrome and severe mitral insufficiency.
Q81342041	Toward an understanding of dural ectasia: a light microscopy study in a murine model of Marfan syndrome
Q81386580	Tracheal compression in Marfan syndrome
Q87247501	Transcatheter aortic valve implantation for a failed bio-bentall in patients with Marfan syndrome
Q85176607	Transscleral intraocular lens fixation with preservation of the anterior vitreous face in patients with marfan syndrome and ectopia lentis
Q37413314	Treating the thoracic aorta in Marfan syndrome: surgery or TEVAR?
Q90437485	Treatment experience of thoracic aortic aneurysm recurrence after multiple surgeries for Marfan syndrome: A case report
Q47976606	Treatment of a chronic aneurysmal aortic dissection in a patient with Marfan syndrome using a staged hybrid procedure and a fenestrated endograft
Q24298608	Treatment of aortic disease in patients with Marfan syndrome
Q70075455	Treatment of ascending aortic dissection in the Marfan syndrome
Q70595983	Treatment of retinal detachment in Marfan syndrome
Q92639850	Trends in spinal deformity surgery in Marfan syndrome
Q95313449	Trends of vascular surgery procedures in Marfan syndrome and Ehlers-Danlos syndrome
Q30399417	Trigeminal neuralgia in a patient with Marfan syndrome: case report
Q91863847	True Aneurysm of the Left Main Trunk in a Marfan Syndrome Patient at Remote Period after Bentall Operation and Total Arch Replacement: A Case Report
Q83520629	True abdominal aortic aneurysm in Marfan syndrome
Q43074603	Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practice
Q99558663	Two Novel Pathogenic FBN1 Variations and Their Phenotypic Relationship of Marfan Syndrome
Q76375092	Two cases of Marfan syndrome
Q54067491	Two cases of Marfan syndrome, surgically treated for complicating spontaneous pneumothorax
Q37084846	Two mutations in Marfan syndrome resulting in truncated fibrillin polypeptides
Q46776444	Two novel and one known mutation of the TGFBR2 gene in Marfan syndrome not associated with FBN1 gene defects.
Q71996189	Two novel mutations and a neutral polymorphism in EGF-like domains of the fibrillin gene (FBN1): SSCP screening of exons 15-21 in Marfan syndrome patients
Q36411995	Two novel mutations of FBN1 in Jordanian patients with Marfan syndrome
Q36766104	Two novel mutations of fibrillin-1 gene correlate with different phenotypes of Marfan syndrome in Chinese families
Q57178700	Two rare missense mutations in the fibrillin‑1 gene associated with atypical cardiovascular manifestations in a Chinese patient affected by Marfan syndrome
Q81385345	Two surgical cases of acute aortic dissection in pregnancy with marfan syndrome
Q48630711	Two-stage correction using the Taylor Spatial Frame for severe hindfoot deformity in a patient with Marfan syndrome: A case report.
Q37588885	Two-stage total cardioaortic replacement for end-stage heart and aortic disease in Marfan syndrome: case report and review of the literature
Q87401756	Type A aortic dissection in Marfan syndrome: a case for more aggressive and extensive surgery at the time of the initial surgical operation
Q87401757	Type A aortic dissection in Marfan syndrome: extent of initial surgery determines long-term outcome
Q88383394	Type A dissections in patients with Marfan syndrome: When less is not more
Q90658215	Ulnar Artery Aneurysm as a Late Sequela of Marfan Syndrome
Q79916309	Ultrastructural pathology of aortic dissections in patients with Marfan syndrome: Comparison with dissections in patients without Marfan syndrome
Q47573364	Uncertainty management and communication preferences related to genetic relativism among families affected by down syndrome, Marfan syndrome, and neurofibromatosis
Q90386189	Undescribed mutations in FBN1 gene in two family cases of Marfan syndrome
Q49074865	Unexpected tracheomalacia in Marfan syndrome during general anesthesia for correction of scoliosis.
Q68099300	Unilateral lens dislocation and axial elongation in Marfan syndrome
Q85704492	Unpredictable coupling: thrombophilia in a patient with Marfan syndrome
Q64039452	Unreliable Estimation of Aortic Pulse Wave Velocity Provided by the Mobil-O-Graph Algorithm-Based System in Marfan Syndrome
Q90147503	Unusual Cause of Heart Failure in a Patient with Marfan Syndrome: A Late Complication of Bioprosthetic Valved Graft Replacement
Q87846920	Unusual association of type A aortic dissection and aberrant right subclavian artery in Marfan syndrome
Q70336430	Unusual echocardiographic findings in the Marfan syndrome
Q88115874	Unusual presentation of adult Marfan syndrome as a complex diaphragmatic hiatus hernia
Q50982609	Unusual presentation of aortic disease in Marfan syndrome: case report.
Q91849964	Update on Clinical Trials of Losartan With and Without β-Blockers to Block Aneurysm Growth in Patients With Marfan Syndrome: A Review
Q89206958	Update on the Diagnosis and Management of Inherited Aortopathies, Including Marfan Syndrome
Q49618820	Urinary Disorders and Marfan Syndrome: A Series of 4 Cases.
Q68375947	Urinary excretion of mucopolysaccharides in normal individuals and in the Marfan syndrome
Q82470846	Urinary incontinence should be added to the manifestation in women with Marfan syndrome
Q92679634	Use of the arm-span to height ratio as a criterion for Marfan syndrome in Aboriginal Australians: Diagnostically challenging
Q79918936	Usefulness of tissue doppler imaging for assessing aortic wall stiffness in children with the Marfan syndrome
Q43714770	Utility of antropological methods in recognition of the Marfan syndrome
Q89417017	Utility of serial 12-lead electrocardiograms in children with Marfan syndrome
Q83076152	Value of molecular diagnosis in a family with Marfan syndrome and an atypical vascular phenotype
Q38495406	Valve-sparing and valve-replacing techniques for aortic root replacement in patients with Marfan syndrome: Analysis of early outcome
Q44865136	Valve-sparing and valve-replacing techniques for aortic root replacement in patients with Marfan syndrome: analysis of early outcome
Q37198132	Valve-sparing aortic root replacement in patients with Marfan syndrome enrolled in the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions.
Q73276751	Valve-sparing aortic root replacement in patients with the Marfan syndrome
Q80172677	Valve-sparing operation in a young woman with Marfan syndrome: a word of caution
Q92091039	Valvular Disease in Marfan Syndrome: Surgical Considerations and Management
Q70406458	Van der Hoeve (Lobstein) and Marfan syndrome in brother and sister
Q67428772	Variable expression of Marfan syndrome in monozygotic twins
Q38706381	Variable severity of cardiovascular phenotypes in patients with an early-onset form of Marfan syndrome harboring FBN1 mutations in exons 24-32.
Q96683695	Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome
Q92669481	Vascular progenitor cell senescence in patients with Marfan syndrome
Q38930482	Vascular smooth muscle cells in Marfan syndrome aneurysm: the broken bricks in the aortic wall.
Q43251221	Vasomotor dysfunction in the thoracic aorta of Marfan syndrome is associated with accumulation of oxidative stress
Q73425808	Veno-occlusive disease in a male patient with Marfan syndrome and common acute lymphoblastic leukemia during induction therapy
Q33163664	Ventricular extrasystole and syncope in a patient with Marfan syndrome
Q73230780	Vermiculate atrophoderma in a boy with Marfan syndrome
Q86648167	Vertebrobasilar dolichoectasia associated with Marfan syndrome
Q84972926	Videocapillaroscopy and Marfan syndrome: a 2-case report
Q79367920	Visceral diverticula and the Marfan syndrome
Q92038417	Visual outcome and surgical results in children with Marfan syndrome
Q55507284	Visualisation of aortic flow disturbance in Marfan syndrome by 4D phase-contrast CMR.
Q87270018	WITHDRAWN: Marfan syndrome: An eyesight of syndrome
Q35684414	Whole exome sequencing confirms the clinical diagnosis of Marfan syndrome combined with X-linked hypophosphatemia
Q53510869	Work participation in adults with Marfan syndrome: Demographic characteristics, MFS related health symptoms, chronic pain, and fatigue.
Q53695907	[30-year-old Patient with suspected Marfan Syndrome and Progressive Gait disturbance].
Q74654017	[A case of Bentall's operation for an 11-year-old patient with Marfan syndrome]
Q78820566	[A case of Marfan syndrome in midtrimester of pregnancy]
Q68718208	[A case of Marfan syndrome with recurrent bilateral pneumothorax and anuloaortic ectasia]
Q83064135	[A case of aortic dissection in an adolescent with Marfan syndrome and surgical treatment]
Q71385229	[A case of bilateral pneumothorax in the patient with Marfan syndrome]
Q69622941	[A case of familial Marfan syndrome without manifested ocular anomalies]
Q69538557	[A case of familial Marfan syndrome]
Q77991841	[A case of mitral valve replacement and left atrial plication for infantile Marfan syndrome with giant left atrium due to mitral valve regurgitation]
Q71385213	[A case of redo operation for ascending aortic aneurysm after modified Bentall operation for Marfan syndrome associated with type A acute dissecting aortic aneurysm]
Q78227808	[A case of sacral meningeal cyst with Marfan syndrome]
Q70438560	[A case of the forme fruste of Marfan syndrome complicated with annulo-aortic ectasia and coarctation of the aorta (author's transl)]
Q73063237	[A case report of total aortic reconstruction and choice of staged operation in Marfan syndrome]
Q87095339	[A pedigree with Marfan syndrome]
Q73773073	[A rare case of Marfan syndrome with involvement of the thoracoabdominal aorta--its surgical treatment]
Q74601986	[A report of three surgical cases in a family of Marfan syndrome]
Q95580729	[A retrospective comparative study of acute type A aortic dissection in patients with Marfan syndrome and bicuspid aortic valves]
Q79513548	[AFBN1 gene in patients with Marfan syndrome]
Q73273237	[Abdominal aortic aneurysm and annuloaortic ectasia in siblings with Marfan syndrome]
Q72063831	[Acute and chronic aortic diseases in Marfan syndrome and arterial hypertension--a comparison of anatomy, clinical aspects and prognosis]
Q54521583	[Acute aortic dissection in a female patient with Marfan syndrome]
Q81157726	[Acute carpal tunnel syndrome in a patient with Marfan syndrome]
Q91630159	[An axillary-subclavian artery aneurysm in pre-rupture revealing Marfan syndrome]
Q52402416	[An unrecognized case of Marfan syndrome: Talleyrand's case].
Q91765635	[Analysis of FBN1 gene mutations in two pedigrees affected with Marfan syndrome]
Q78342878	[Anesthesia for section caesarean with aortic dissection in Marfan Syndrome]
Q86335130	[Anesthetic Management of Right Lower Lobectomy in a Patient with Marfan Syndrome]
Q86316461	[Anesthetic Management of a Patient Complicated with Marfan Syndrome and Suffering from Stanford Type A Aortic Dissection during Pregnancy]
Q68041685	[Aneurysm of the internal carotid artery and cervical mega-dolicho-arteries in Marfan syndrome]
Q83912776	[Aneurysm of the radial artery in a patient with marfan syndrome]
Q77698915	[Anthropometric parameters in assessment of patients with Marfan syndrome or with Marfan phenotype]
Q56978091	[Aortic disease in Marfan syndrome: current role of surgery and thoracic endovascular aortic repair]
Q77057043	[Aortic dissecting aneurysm in a patient with Marfan syndrome and an artificial aortic valve]
Q90068083	[Aortic dissection at three years post aortic replacement in a patient with Marfan syndrome complicating with abdominal aortic aneurysm: a case report]
Q74601988	[Aortic dissection in pregnant woman with the Marfan syndrome]
Q51296260	[Aortic root dilatation rate in pediatric patients with Marfan syndrome treated with losartan].
Q79739747	[Aortic root replacement in Marfan syndrome with hemophilia A]
Q80399766	[Aortic valve sparing for aortic root aneurysm in patients with Marfan syndrome]
Q74601969	[Aortic valve-sparing root reconstruction in Marfan syndrome]
Q68708342	[Cardiac tamponade caused by rupture of a dissecting aortic aneurysm to the pericardial sac in a patient with Marfan syndrome]
Q70441422	[Cardiovascular changes in the Marfan syndrome]
Q78419910	[Cardiovascular manifestations in the course of Marfan syndrome]
Q84883671	[Cardiovascular manifestations of Marfan syndrome]
Q74601978	[Cardiovascular surgery in patients with Marfan syndrome]
Q50516611	[Case of Marfan syndrome with microscopic hematuria].
Q71212753	[Characteristic findings of mitral valve and mechanism of mitral valve prolapse in Marfan syndrome]
Q80792223	[Clinical analysis of pregnancy and postpartum cardiovascular complications in Marfan syndrome]
Q59694006	[Clinical aspects of Marfan syndrome]
Q54424010	[Compliance of the normal-sized aorta in adolescents with Marfan syndrome: comparison of MR measurements of aortic distensibility and pulse wave velocity]
Q54022628	[Concomitant graft replacement of the total aortic root and the transverse aortic arch for type A aortic dissection associated with Marfan syndrome: report of a case]
Q86406026	[Concurrence of Marfan syndrome and urinary tract deformities in a neonate]
Q69593076	[Congenital absence of pericardium in a case of a variant of Marfan syndrome]
Q74547932	[Contribution of genetics to pathogenicity and diagnosis of Marfan syndrome]
Q74601961	[Corrective surgery for pectus excavatum in patients with Marfan syndrome]
Q95430786	[Current status and future perspectives in the research of Marfan syndrome]
Q45903816	[Detection of pathogenic mutations in Marfan syndrome by targeted next-generation semiconductor sequencing].
Q84977650	[Diagnosis and options for reconstructive heart valve surgery in the Marfan syndrome]
Q68822153	[Diagnosis of dissecting aortic aneurysm in Marfan syndrome]
Q69434042	[Disorders of spinal circulation in Marfan syndrome]
Q68830185	[Dissecting aneurysm of the common iliac artery in Marfan syndrome: rupture following sports activities]
Q78545801	[Dolichomorphia (Marfan syndrome) and ectodermal dysplasias]
Q82622966	[Dural ectasia and lumbar pain associated with Marfan syndrome]
Q93104258	[Early and Midterm Results of Thoracoabdominal Aortic Aneurysm Repair in Patients with Marfan Syndrome]
Q81062634	[Epidural, mediastinal and subcutaneous emphysema in a patient with suspected torme fruste of Marfan syndrome]
Q88124491	[Exceptional association of bilateral popliteal aneurysm with an abdominal aortic aneurysm in Marfan syndrome]
Q84584975	[Experience with a fresh aortic homograft employed in a patient with acute dissection of the ascending portion of the aorta and Marfan syndrome]
Q80790088	[Extracranial internal carotid artery aneurysm associated with Marfan syndrome: case report]
Q95537852	[Familial Annulo-aortic Ectasia without Marfan Syndrome]
Q54530632	[Fatal Marfan syndrome in the neonatal period]
Q78962752	[Fibrillin-1 gene mutation in Chinese patients with Marfan syndrome and its gene diagnosis by haplotype analysis]
Q74223154	[Genetic aspects of Marfan syndrome]
Q82279815	[Genetic testing for Marfan syndrome]
Q86103334	[Genetics and prevention of genetic aortic syndromes (GAS) and of the Marfan syndrome]
Q54343609	[Genotypic characterization of a Portuguese population of Marfan syndrome patients].
Q70957045	[Glaucoma in Marfan syndrome: position-dependent measurement of intraocular pressure as a diagnostic criterium]
Q74220568	[Heart-lung transplantation and the Marfan syndrome]
Q95621586	[High-risk pregnancy in a woman with Marfan syndrome, a bicuspid aortic valve, and a dilated aortic sinus]
Q91189793	[Identification of a novel FBN1 variant in a pedigree affected with Marfan syndrome]
Q85015966	[Images in cardiology after clinical observation - aortic dissection in Marfan syndrome]
Q78528575	[Incidence of Marfan syndrome in cardiovascular diseases]
Q73248645	[Indirect genotype analysis as a diagnostic procedure in Marfan syndrome]
Q72708968	[Isolated proximal fibula fracture in Marfan syndrome]
Q87032747	[Late onset lens particle glaucoma in Marfan syndrome]
Q90795892	[Living with… Marfan syndrome]
Q50164831	[Marfan Syndrome: new diagnostic criteria, same anesthesia care? Case report and review].
Q75531694	[Marfan syndrome (arachnodactylia and ectopia lentis) with special reference to ocular symptoms and heredity.]
Q73908265	[Marfan syndrome (arachnodactyly)]
Q73536748	[Marfan syndrome and abdominal aneurysm]
Q70780154	[Marfan syndrome and aneurysm of the abdominal aorta]
Q83377907	[Marfan syndrome and aortic dissection during pregnancy]
Q71150028	[Marfan syndrome and diaphragmatic hernia]
Q70667000	[Marfan syndrome and giant intracranial aneurysms: report of a case]
Q77592949	[Marfan syndrome and heart valve diseases]
Q68038054	[Marfan syndrome and pregnancy, complicated by dissecting aneurysm]
Q69095683	[Marfan syndrome and pregnancy. A life-threatening combination?]
Q70552598	[Marfan syndrome and pregnancy]
Q70691344	[Marfan syndrome and pregnancy]
Q72022692	[Marfan syndrome and pregnancy]
Q77518056	[Marfan syndrome and pregnancy]
Q78221220	[Marfan syndrome and pregnancy]
Q52960621	[Marfan syndrome and valvular disease].
Q85653781	[Marfan syndrome associated with aortic dissection, venous thromboembolism and hyperhomocysteinemia]
Q84028477	[Marfan syndrome complicated with CD5+ CD10+ diffuse large B-cell lymphoma]
Q73773089	[Marfan syndrome in a family]
Q81624371	[Marfan syndrome in a practice of a cardiologist: diagnosis, treatment, possibility of pregnancy and delivery]
Q70116003	[Marfan syndrome in a pregnant woman]
Q95514217	[Marfan syndrome in childhood and adolescence]
Q67916194	[Marfan syndrome in childhood: cardiovascular manifestations. Echocardiographic changes]
Q79844339	[Marfan syndrome in pregnancy: presentation of four cases and discussion]
Q70726610	[Marfan syndrome in the light of observed cases]
Q74368648	[Marfan syndrome in the newborn and infants less than 4 months: a series of 9 patients]
Q83605309	[Marfan syndrome needed several repetitive emergency operations in short time]
Q86046657	[Marfan syndrome presenting with cervical tortuous arteries and subcortical hemorrhage: a case with a mutation in an intron of the FBN1 gene]
Q70036913	[Marfan syndrome with absolute glaucoma and secondary unilateral scleral ectasis]
Q74506901	[Marfan syndrome, a case report]
Q78526061	[Marfan syndrome, pseudotruncus arteriosus and brain abscess]
Q53666694	[Marfan syndrome: clinical and pathomorphological restructurings after surgical treatment of aortic aneurysm].
Q74542909	[Marfan syndrome: diagnosis of cardiovascular manifestations]
Q81531778	[Marfan syndrome: diagnostic criteria and molecular biology contribution]
Q53638454	[Marfan syndrome: pathogenesis, phenotypes and diagnostic value, of various imaging techniques]
Q74542904	[Marfan syndrome: prevalence and natural course of cardiovascular manifestations]
Q74182623	[Marfan syndrome: strategies of interdisciplinary care]
Q74542913	[Marfan syndrome: therapy of cardiovascular manifestations]
Q75554626	[Marfan syndrome; presentation of a case]
Q80620878	[Marfan syndrome; report of a new case]
Q93375760	[Maternal mortality among women with Marfan syndrome or vascular Ehlers-Danlos syndrome in France, 2001-2012]
Q71647798	[Mitral insufficiency in Marfan syndrome]
Q72257717	[Mitral valve replacement and closure of atrial septal defect in the case associated with Marfan syndrome]
Q86370052	[Morgagni-Larrey diaphragmatic hernia in a 3-month-old child affected by Marfan syndrome]
Q81531808	[Multidisciplinary management and paediatric Marfan syndrome]
Q86063009	[Mutation analysis and prenatal diagnosis of FBN1 gene mutations for four patients with Marfan syndrome]
Q89085517	[Mutation analysis of FBN1 gene in a child with Marfan syndrome]
Q68047649	[Natural and recombinant interferons provide different protection of human cells with impaired repair system (Marfan syndrome) against mutagens]
Q73549904	[Neonatal heart failure and Marfan syndrome]
Q73408904	[Neurological disorders in Marfan syndrome]
Q49171864	[New diagnostic criteria in Marfan syndrome]
Q85222145	[Novel pharmacological strategies for aortic dilation in Marfan syndrome: from mouse models to human patients]
Q73178857	[Observations of a combination of subchondral disturbances of the ossification of cartilage, Marfan syndrome and dysostosis multiplex]
Q70544400	[Ocular histopathologic study of Marfan syndrome in a newborn infant]
Q71148920	[One stage operation of sternal turnover and Bentall operation for a case of severe Marfan syndrome]
Q73145971	[One-stage correction of heart defect and funnel chest in the Marfan syndrome]
Q80104562	[One-staged operation for mitral regurgitation and annuloaortic ectasia without aortic regurgitation with Marfan syndrome; report of a case]
Q71087667	[Orthostatic dysregulation in Marfan syndrome]
Q95542861	[Pathogenesis of the Marfan syndrome]
Q95546101	[Patients with aneurysms and osteoarthritis: Marfan syndrome ruled out, so what is it?]
Q53724533	[Post-cesarean acute aortic dissection in a Marfan syndrome patient].
Q69477025	[Post-traumatic dissecting aneurysm of the aorta occurring in Marfan syndrome: report of an autopsy case]
Q81033642	[Prevalence of cardiovascular manifestations in Marfan syndrome]
Q73484378	[Preventive concomitant aortic root replacement for annuloaortic ectasia in a patient with Marfan syndrome undergoing mitral valve replacement for mitral regurgitation]
Q74601982	[Prognosis and percentage of employment after the surgery in Marfan syndrome]
Q69443520	[Pronounced cardiovascular, osseous and ophthalmologic changes in a patient with Marfan syndrome]
Q91988621	[ROLE OF TGFβ-INDUCTION AND GASTROINTESTINAL MYOFIBROBLASTS IN PATHOMORPHOGENESIS OF CHRONIC GASTRITIS IN PATIENTS WITH MARFAN SYNDROME AND MARFAN-LIKE STATES]
Q54634347	[Rare constellation of findings in Marfan syndrome in MR tomography]
Q83727470	[Recent progress in Marfan syndrome]
Q74601983	[Reconstruction of aortic branches after total aortic replacement in Marfan syndrome; report of a case]
Q92754182	[Research advances on the pathogenesis of Marfan syndrome]
Q70748163	[Rupture of the common hepatic artery in Marfan syndrome]
Q52978792	[Safe and Effective Analgesia with Bilateral Continuous TAP Block for a Patient with Marfan Syndrome after Open Abdominal Aortic Aneurysm Repair].
Q56778766	[Screening of FBN1 gene mutations in a family with Marfan syndrome]
Q81633214	[Serial clinical and echocardiographic evaluation in children with Marfan syndrome]
Q75426232	[Skeletal and occlusal alterations in the diagnosis of Marfan syndrome]
Q81531782	[Spinal deformities in Marfan syndrome]
Q70274058	[Spontaneous pneumothorax in Marfan syndrome: presentation of a clinical case]
Q81772860	[Successful consecutive seven time's surgical repair of Marfan syndrome]
Q86207844	[Successful endovascular stent-graft treatment in a patient with Marfan syndrome presenting with complicated acute Type B dissection]
Q77317540	[Successful surgical treatment for severe mitral valve annulus enlargement and mitral regurgitation 5 years after aortic root replacement in Marfan syndrome: a case report]
Q80343382	[Sudden death and cardiovascular complications in Marfan syndrome: impact of surgical intervention]
Q71385176	[Surgery for acute type A aortic dissection associated with Marfan syndrome]
Q94561790	[Surgical Treatment of Pectus Excavatum in Patients with Marfan Syndrome Associated with Vertebral or Cardiovascular Disease]
Q58120763	[Surgical correction of contractural arachnodactyly deformity of a child with Marfan syndrome]
Q74601964	[Surgical treatment for proximal ascending aortic lesion in Marfan syndrome; retrospective evaluation of the initial surgical technique at late reoperation]
Q74601972	[Surgical treatment of Marfan syndrome; late results and new strategy]
Q81624383	[Surgical treatment of a patient with aneurysm of ascending aorta and involvement of three cardiac valves due to Marfan syndrome]
Q68026767	[Surgical treatment of aneurysm of the ascending aorta in Marfan syndrome]
Q72794526	[Surgical treatment of cardiovascular manifestations of Marfan syndrome]
Q74601974	[Surgical treatment of cardiovascular manifestations of Marfan syndrome]
Q81560140	[Surgical treatment of the aortic root aneurysm related to Marfan syndrome]
Q74601987	[Surgical treatment of two cases with Marfan syndrome]
Q68678306	[Surgically treated aneurysm of the abdominal aorta in a patient with Marfan syndrome]
Q80663067	[Survival and complications in remote period of follow-up in patients with Marfan syndrome after correction of aneurism of the ascending aorta and aortic insufficiency]
Q54261882	[The Marfan syndrome (clinical, histopathological and genetic study of a case)]
Q70731533	[The Marfan syndrome with a small body (author's transl)]
Q69787959	[The coexistence of rheumatoid arthritis and systemic lupus erythematosus accompanied with Marfan syndrome (forme fruste) in two sisters]
Q69544356	[The diagnosis and treatment of cardiovascular disorders in Marfan syndrome]
Q77316046	[The early diagnosis of the Marfan syndrome in servicemen]
Q83799767	[The establishment of the Marfan syndrome biobank in Hungary - Erratum]
Q49033764	[The establishment of the Marfan syndrome biobank in Hungary].
Q84188223	[The morphology and thickness of cornea in patients with Marfan syndrome]
Q81750501	[The research progress in Marfan syndrome]
Q74547935	[Thoracic aortic aneurysm in Marfan syndrome]
Q73222409	[Total proximal reconstruction of chronic aortic dissection in patients with Marfan syndrome]
Q70563016	[Two cases of Marfan syndrome complicated with aortic dissection during pregnancy]
Q73112919	[Two cases of Marfan syndrome]
Q80752355	[Two gene mutations in fibrillin 1 of Marfan syndrome]
Q81106156	[Two novel mutations in fibrillin-1 gene of Marfan syndrome]
Q88580415	[Unclear right atrial tumor in a 40-year-old patient with Marfan syndrome]
Q90975679	[Valve sparing aortic root replacement (David Procedure) in 36 year - old woman with the Marfan syndrome at the 27th week of pregnancy]
Q84719840	[Valve-sparing aortic root replacement for young female patients with Marfan syndrome]
Q83147251	[Vascular malformations associated with Marfan syndrome, Ehlers-Danlos syndrome and neurofibromatosis 1 and their surgical treatment]
Q52969169	[Ventricular septal aneurysm in a patient with Marfan syndrome]
Q35089538	β-Blockers and angiotensin converting enzyme inhibitors: comparison of effects on aortic growth in pediatric patients with Marfan syndrome

rare disease	Q929833
designated intractable/rare disease	Q42303753
class of disease	Q112193867
symptom or sign	Q112965645

disease	Q12136
connective tissue disease	Q1779300
eye disease	Q3041498
marfanoid	Q6759035

P8313	Den Store Danske ID	Marfans_syndrom
P699	Disease Ontology ID	DOID:14323
P557	DiseasesDB	7845
P673	eMedicine ID	1258926
		946315
P10565	Encyclopedia of China (Third Edition) ID	577307
P1417	Encyclopædia Britannica Online ID	science/Marfan-syndrome
P3219	Encyclopædia Universalis ID	maladie-de-marfan
P2888	exact match	http://identifiers.org/doid/DOID:14323
		http://purl.obolibrary.org/obo/DOID_14323
		http://www.orpha.net/ORDO/Orphanet_558
P1325	external data available at URL	http://www.nanbyou.or.jp/entry/4792
P646	Freebase ID	/m/0cc6n
P4317	GARD rare disease ID	6975
P668	GeneReviews ID	NBK1335
P7464	Genetics Home Reference Conditions ID	marfan-syndrome
P227	GND ID	4168872-7
P4229	ICD-10-CM	Q87.4
		Q87.40
P7807	ICD-11 (foundation)	236564145
P7329	ICD-11 ID (MMS)	LD28.01
P1692	ICD-9-CM	759.82
P667	ICPC 2 ID	A90
P3827	JSTOR topic ID	marfan-syndrome
P8408	KBpedia ID	MarfansSyndrome
P665	KEGG ID	H00653
P604	MedlinePlus ID	000418
		000418
P486	MeSH descriptor ID	D008382
P672	MeSH tree code	C05.116.099.674
		C14.240.400.725
		C14.280.400.725
		C16.131.077.550
		C16.131.240.400.720
		C16.320.540
		C17.300.500
P5270	Mondo ID	MONDO_0007947
P1748	NCI Thesaurus ID	C34807
P7995	NHS Health A to Z ID	marfan-syndrome
P492	OMIM ID	154700
		154700
P10283	OpenAlex ID	C2780561598
P1550	Orphanet ID	558
P1461	Patientplus ID	marfans-syndrome-pro
P4233	PatientsLikeMe condition ID	marfan-s
P3417	Quora topic ID	Marfan-Syndrome
P3984	subreddit	marfans
P2892	UMLS CUI	C0024796
		C4721845
P11430	UniProt disease ID	DI-00699
P11143	WikiProjectMed ID	Marfan syndrome
P3471	WikiSkripta article ID	3057
P2347	YSO ID	15804

P689	afflicts	connective tissue	Q25615
P2293	genetic association	FBN1	Q17927651
P1995	health specialty	medical genetics	Q1071953
P138	named after	Antoine Marfan	Q586765
P5008	on focus list of Wikimedia project	WikiProject Medicine	Q4099686
P780	symptoms and signs	pectus carinatum	Q164218
		scoliosis	Q174857
		pectus excavatum	Q431168
		ectopia lentis	Q1827028
		aortic dissection	Q594660
		aortic aneurysm	Q616003
		flat feet problems	Q653200
		mitral valve prolapse	Q735652
		dolichostenomelia	Q5289085

Q64720524	A Randomized, Open-label, LOSARTAN Therapy on the Progression of Aortic Root Dilation in Patients With Marfan Syndrome
Q61918515	Angiotensin Converting Enzyme Inhibitors in Marfan Syndrome
Q63836787	Aortopathy in Persons With Bicuspid Aortic Valve, Turner and Marfan Syndrome
Q93328805	Arithmetic Abilities in Children With 22q11.2DS
Q63831111	Atenolol Versus Losartan in the Prevention of Progressive Dilation of the Aorta in Marfan Syndrome
Q63011212	Cardiorespiratory and Muscular Rehabilitation of Children and Young Adults With Marfan Syndrome.
Q63397931	Children and Adolescents With Marfan Syndrome: 10,000 Healthy Steps and Beyond
Q63335271	Circulating Transforming Growth Factor Beta (TGF-β) in Individuals With Marfan Syndrome
Q89155129	Classifying Ectopia Lentis in Marfan Syndrome Into Five Grades of Increasing Severity
Q61707490	Clinical Variability in Marfan Syndrome
Q64653706	Cognitive Remediation in 22q11DS
Q64639472	Comparison of Aliskiren vs Negative Controls on Aortic Stiffness in Patients With MFS
Q63339294	Comparison of Medical Therapies in Marfan Syndrome.
Q61921194	Comparison of Two Medications Aimed at Slowing Aortic Root Enlargement in Individuals With Marfan Syndrome--Pediatric Heart Network
Q64677278	Computerized Cognitive Skills Training for Adolescents With Velocardiofacial Syndrome
Q65356230	Development of a Blood Test for Marfan Syndrome
Q105493317	Effect on the Quality of Life of a Therapeutic Education Program in Patients With Marfan Syndrome
Q64717030	Effects of Losartan Versus Atenolol on Aortic and Cardiac Muscle Stiffness in Adults With Marfan Syndrome
Q99956432	Effects of Personalized Training at Home Combining Endurance and Resistance in Patients Suffering From Marfan Syndrome
Q65380397	Examining Genetic Factors That Affect the Severity of 22q11.2 Deletion Syndrome
Q66402679	Expanded Noninvasive Genomic Medical Assessment: The Enigma Study
Q64171995	First Trimester Screening for Trisomy 21, 18, 13 and 22q11.2 Deletion Syndrome
Q445270	Flo Hyman
Q66400087	Generation of Marfan Syndrome and Fontan Cardiovascular Models Using Patient-specific Induced Pluripotent Stem Cells
Q64677318	Genetic Modifiers for 22q11.2 Syndrome
Q66027366	Genetics and Psychopathology in the 22q11 Deletion Syndrome
Q12623930	Han Ki-bum
Q61741021	Holkje van der Veer
Q66060593	Immunologic Evaluation in Patients With DiGeorge Syndrome or Velocardiofacial Syndrome
Q65539006	Infection in DiGeorge Following CHD Surgery
Q14327750	Isaiah Austin
Q3163137	Javier Botet
Q312387	Joey Ramone
Q11604296	Kenshi Yonezu
Q113914964	Living With Marfan Syndrome and Your Aorta
Q113916539	Living With Marfans and Your Aorta: Surgical Outcomes Study
Q64724857	Losartan Versus Atenolol for the Treatment of Marfan Syndrome
Q105089518	Marfan Syndrome Moderate Exercise Pilot
Q65352528	Micro RNAs as a Marker of Aortic Aneurysm in Hereditary Aortopathy Syndromes
Q64710472	Middle and Inner Ear Malformation in Children With Velocardiofacial Syndrome
Q113921254	Mortality and Morbidity Outcomes in Marfans
Q63335971	National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions
Q65378195	Nebivolol Versus Losartan Versus Nebivolol+Losartan Against Aortic Root Dilation in Genotyped Marfan Patients
Q65331811	Non-Invasive Chromosomal Evaluation of 22q11.2
Q65378825	Parathyroid and Thymus Transplantation in DiGeorge #931
Q63401057	Pathogenetic Basis of Aortopathy and Aortic Valve Disease
Q64726910	Phase I/II Thymus Transplantation With Immunosuppression #950
Q79110757	Pregnancy in Women With Rare Multisystemic Vascular Diseases: COGRare5 Study
Q64710629	Randomized, Double-blind Study for the Evaluation of the Effect of Losartan Versus Placebo on Aortic Root Dilatation in Patients With Marfan Syndrome Under Treatment With Beta-blockers
Q65347034	Resolution of Primary Immune Defect in 22q11.2 Deletion Syndrome
Q64398222	SNP-based Microdeletion and Aneuploidy RegisTry (SMART)
Q66082896	Safety and Efficacy Study of NFC-1 in Subjects Aged 12-17 Years With 22q11.2DS & Associated Neuropsychiatric Conditions
Q66064838	Sleep Disordered Breathing in Marfan Syndrome: Susceptibility and Hemodynamics
Q64188492	Social Cognition Training and Cognitive Remediation
Q65540227	Studies of Heritable Disorders of Connective Tissue
Q66061111	Study of Heritable Connective Tissue Disorders
Q66062034	Study of Phenotype and Genotype Correlations in Patients With Contiguous Gene Deletion Syndromes
Q65377860	Study of the Efficacy of Losartan on Aortic Dilatation in Patients With Marfan Syndrome
Q3976680	Sue Geh
Q64795059	Tele-Clinic Visits in Pediatric Marfan Patients Using Parental Echo: The Future?
Q86294507	The Oscillation of Crystalline and Intraocular Lenses
Q64354188	The Oxford Marfan Trial
Q64716151	The Psychiatric and Cognitive Phenotypes in Velocardiofacial Syndrome
Q65358811	Thoracic Aortic Dilatation Syndromes
Q65378649	Thymus Transplantation Dose in DiGeorge #932
Q63817789	Thymus Transplantation Safety-Efficacy
Q64726891	Thymus Transplantation With Immunosuppression
Q64727354	Thymus Transplantation in DiGeorge Syndrome #668
Q1362028	Troye Sivan
Q62105798	Velocardiofacial (VCFS; 22q11.2; DiGeorge) Syndrome Study

Marfan syndrome

genetic disorder of the connective tissue

Reverse relations

The articles in Wikimedia projects and languages

Q54751866	AU10176
Q54751868	AU10177
Q54749546	Am Tim
Q54749848	An Bay
Q54749893	An Zan
Q54750334	Ar Bo
Q54795843	Be Cal
Q123030949	CMGANTi005-A
Q123030953	CMGANTi008-A
Q93455820	CMUi001-A
Q54809085	Ce Geg
Q54830943	De Te
Q54834901	FIB-MARFAN1
Q54834902	FIB-MARFAN3
Q54834903	FIB-MARFAN4
Q54834904	FIB-MARFAN5
Q54834905	FIB-MARFAN6
Q54834991	Flo Tel
Q54835993	GM00035
Q54835994	GM00036
Q54842874	GM07726
Q54842875	GM07727
Q54844467	GM10433
Q54844488	GM10486
Q54844543	GM10559
Q54844592	GM10691
Q54844593	GM10692
Q54844596	GM10695
Q54844632	GM10748
Q54851945	GM21498
Q54851946	GM21499
Q54852223	GM21931
Q54852224	GM21932
Q54852225	GM21934
Q54852226	GM21935
Q54852227	GM21936
Q54852228	GM21937
Q54852230	GM21938
Q54852231	GM21939
Q54852232	GM21940
Q54852233	GM21941
Q54852234	GM21942
Q54852235	GM21943
Q54852236	GM21944
Q54852237	GM21945
Q54852238	GM21946
Q54852239	GM21947
Q54852240	GM21948
Q54852241	GM21950
Q54852242	GM21951
Q54852243	GM21952
Q54852244	GM21953
Q54852251	GM21954
Q54852252	GM21956
Q54852253	GM21957
Q54852254	GM21958
Q54852255	GM21960
Q54852256	GM21966
Q54852257	GM21967
Q54852258	GM21968
Q54852259	GM21969
Q54852260	GM21970
Q54852261	GM21971
Q54852262	GM21972
Q54852263	GM21974
Q54852264	GM21976
Q54852265	GM21978
Q54852266	GM21979
Q54852267	GM21982
Q54852268	GM21983
Q54852269	GM21984
Q54852270	GM21987
Q54852271	GM21988
Q54852272	GM21989
Q54852273	GM21990
Q54852274	GM21992
Q54852275	GM21994
Q107115195	GM28019
Q107115196	GM28020
Q107115200	GM28023
Q54882192	He Geg
Q54898306	ISMMSi001-A
Q54898307	ISMMSi001-B
Q54898308	ISMMSi002-A
Q54898317	ISMMSi002-B
Q54899026	Jo Zan
Q108820666	LANCEi021-A
Q108820667	LANCEi022-A
Q54902396	Le Ana
Q54905401	MFS5
Q54903674	Ma Not
Q54904011	Mar Nol
Q54904075	May Roy
Q95992665	NCCDFWi001-A
Q112930164	NCCDFWi001-A-1
Q108821196	QDMHi001-A
Q54949902	RG-154
Q54949071	Ra Bot
Q54949072	Ra Lot
Q112044513	SC
Q54970627	STR-I-301-MFS
Q98133019	SZ-Marfan7
Q123033695	UGENTi001-A-1
Q54991056	UM89-1 PGD
Q54991061	UM89-4 PGD
Q54993393	VUB08_MFS
Q54993415	VUB28_HD_MFS
Q54993495	Wa Fen
Q108821561	ZJUi005-A
Q112930591	ZJUi009-A
Q105511894	ZZUSAHi003-A
Q54811999	chHES-419

Q3508570	MASS syndrome	subclass of	P279
Q72078511	Bilateral Renal Vein Thrombosis and Nephrotic Syndrome in a Patient with the Marfan Syndrome	cites work	P2860
Q61679550	Steinberg sign	suggests the existence of	P5132

	Category:Marfan syndrome	wikimedia
Arabic (ar / Q13955)	متلازمة مارفان	wikipedia
az	Marfan sindromu	wikipedia
azb	مارفان سندروم	wikipedia
	Marfanov sindrom	wikipedia
Catalan (ca / Q7026)	Síndrome de Marfan	wikipedia
ckb	کۆنیشانی مارفان	wikipedia
	Marfanův syndrom	wikipedia
	Marfans syndrom	wikipedia
	Marfan-Syndrom	wikipedia
	Σύνδρομο Μαρφάν	wikipedia
	Marfan syndrome	wikipedia
en-simple	Marfan Syndrome	wikipedia
	Síndrome de Marfan	wikipedia
Basque language (eu / Q8752)	Marfan sindrome	wikipedia
Persian (fa / Q9168)	نشانگان مارفان	wikipedia
	Marfanin oireyhtymä	wikipedia
	Syndrome de Marfan	wikipedia
ga	Siondróm Marfan	wikipedia
	תסמונת מרפן	wikipedia
	Marfan-szindróma	wikipedia
	Մարֆանի համախտանիշ	wikipedia
	Sindrom Marfan	wikipedia
	Marfan-heilkenni	wikipedia
	Sindrome di Marfan	wikipedia
	マルファン症候群	wikipedia
	მარფანის სინდრომი	wikipedia
	Марфан ауруы	wikipedia
	마르판 증후군	wikipedia
lij	Mouttia de Marfan	wikipedia
	Marfāna sindroms	wikipedia
mk	Марфанов синдром	wikipedia
	Sindrom Marfan	wikipedia
nb	Marfans syndrom	wikipedia
	Syndroom van Marfan	wikipedia
Norwegian, Nynorsk (nn / Q25164)	Marfans syndrom	wikipedia
or	ମାର୍ଫାନ୍ ସିଣ୍ଡ୍ରୋମ୍	wikipedia
pa	ਮਾਰਫਨ ਸਿੰਡਰੋਮ	wikipedia
	Zespół Marfana	wikipedia
pms	Sìndrom ëd Marfan	wikipedia
	Síndrome de Marfan	wikipedia
	Sindromul Marfan	wikipedia
	Синдром Марфана	wikipedia
	Marfanov syndróm	wikipedia
	Марфанов синдром	wikipedia
	Marfans syndrom	wikipedia
ta	மார்வன் நோய்த்தொகை	wikipedia
	กลุ่มอาการมาร์แฟน	wikipedia
	Marfan sendromu	wikipedia
Tatar language (tt / Q25285)	Марфан синдромы	wikipedia
	Синдром Марфана	wikipedia
uz	Marfan sindromi	wikipedia
	Hội chứng Marfan	wikipedia
	馬凡氏症候群	wikipedia

Q445270	Flo Hyman
Q30673332	Pak Song