| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1056/NEJM197904053001406 |
| P953 | full work available at URL | http://www.nejm.org/doi/pdf/10.1056/NEJM197904053001406 |
| P698 | PubMed publication ID | 370588 |
| P2093 | author name string | V. A. McKusick | |
| R. E. Pyeritz | |||
| P2860 | cites work | The American Review of Respiratory Disease | Q26839505 |
| Fragile lung in the Marfan syndrome | Q36441547 | ||
| Formes frustes of Marfan's syndrome presenting with severe aortic regurgitation. Clinicogenetic study of 18 families | Q36799430 | ||
| Replacement of the Ascending Aorta and Aortic Valve with a Composite Graft: Results in 25 Patients | Q39820583 | ||
| Echocardiographic recognition of silent aortic root dilatation in Marfan's syndrome | Q44042236 | ||
| β-Aminopropionitrile-induced dissecting aneurysms of turkeys: Treatment with propranolol | Q44280116 | ||
| The wrist sign. A useful physical finding in the Marfan syndrome | Q45056907 | ||
| Aortic root dilatation and mitral valve prolapse in Marfan's syndrome: an ECHOCARDIOgraphic study | Q45177257 | ||
| THE METACARPAL INDEX. A USEFUL AID IN THE DIAGNOSIS OF THE MARFAN SYNDROME. | Q46422900 | ||
| Postural changes in left ventricular and mitral valvular dynamics in the systolic click - late systolic murmur syndrome | Q66906297 | ||
| Life Expectancy and Causes of Death in the Marfan Syndrome | Q67289418 | ||
| Echocardiography in Marfan's Syndrome | Q67431584 | ||
| Echocardiographic manifestation of annuloaortic ectasia: its "paradoxical" motion of the aorta and premature systolic closure of the aortic vale | Q67554030 | ||
| Ocular Manifestations in the Marfan Syndrome and Homocystinuria | Q69383531 | ||
| Cardiac Manifestations of Marfan Syndrome in Infancy and Childhood | Q69492213 | ||
| Parental age effects on the occurrence of new mutations for the Marfan syndrome | Q70480654 | ||
| The Marfanoid Hypermobility Syndrome | Q72426118 | ||
| A simple screening test for the Marfan syndrome | Q72850096 | ||
| The cardiovascular aspects of Marfan's syndrome: a heritable disorder of connective tissue | Q78580575 | ||
| P433 | issue | 14 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Marfan syndrome | Q208562 |
| P304 | page(s) | 772-777 | |
| P577 | publication date | 1979-04-01 | |
| 1979-04-05 | |||
| P1433 | published in | The New England Journal of Medicine | Q582728 |
| P1476 | title | The Marfan syndrome: diagnosis and management | |
| The Marfan Syndrome: Diagnosis and Management | |||
| P478 | volume | 300 |
| Q64039865 | 3D evaluation of maxillary morphology in Marfan growing subjects: a controlled clinical study |
| Q33590981 | A 26-year review of pectus deformity repairs, including simultaneous intracardiac repair |
| Q35643001 | A Gly1127Ser mutation in an EGF-like domain of the fibrillin-1 gene is a risk factor for ascending aortic aneurysm and dissection. |
| Q42431508 | A case of Marfan syndrome with acute monoblastic leukemia |
| Q37869693 | A family with abdominal aortic aneurysms |
| Q36437954 | A genome-wide association study identifies four novel susceptibility loci underlying inguinal hernia |
| Q33593705 | A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an International Consortium study. |
| Q34219428 | A mutation in FBN1 disrupts profibrillin processing and results in isolated skeletal features of the Marfan syndrome |
| Q92471897 | A network analysis revealed the essential and common downstream proteins related to inguinal hernia |
| Q36099630 | A second locus for Marfan syndrome maps to chromosome 3p24.2-p25. |
| Q42053089 | A surgical case of acute three-channeled aortic dissection in Marfan syndrome |
| Q38053510 | A systematic review of the pharmacological management of aortic root dilation in Marfan syndrome. |
| Q84609501 | A teenager with Marfan syndrome and left ventricular noncompaction |
| 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. |
| Q35832495 | Abnormal fibrillin metabolism in bovine Marfan syndrome. |
| Q49144384 | Abnormal mechanical properties of the aorta in Marfan's syndrome. |
| Q71869726 | Absorption Pharmacokinetics of Atenolol in Patients with the Marfan Syndrome |
| Q34449882 | Acute thoracic aortic dissection: the basics. |
| Q44281051 | An FBN1 pseudoexon mutation in a patient with Marfan syndrome: confirmation of cryptic mutations leading to disease |
| Q33597148 | An exclusion map of Marfan syndrome |
| Q48194218 | An iPSC-derived vascular model of Marfan syndrome identifies key mediators of smooth muscle cell death |
| Q50227247 | An oblique bitoric rigid contact lens fitting for the management of lens subluxation in Marfan syndrome. |
| Q51791068 | Anaesthesia and Marfan's syndrome: case report. |
| Q51558837 | Anaesthesia for caesarean section in a Marfan patient with recurrent aortic dissection. |
| Q48338887 | Anesthetic management of a rare case of Shprintzen–Goldberg craniosynostosis syndrome |
| Q77588809 | Aneurysms of the ascending aorta: diagnostic features and prognosis in patients with Marfan's syndrome versus hypertension |
| Q38285956 | Animal models of scoliosis |
| Q39797031 | Aortic dilation, dissection, and rupture in patients with Turner syndrome |
| Q69516662 | Aortic dissection |
| Q87961495 | Aortic dissection |
| Q56762316 | Aortic dissection and patent ductus arteriosus in three generations |
| Q77339055 | Aortic dissection extending from ductus diverticulum aneurysm |
| Q56655663 | Aortic root dilatation among young competitive athletes: echocardiographic screening of 1929 athletes between 15 and 34 years of age |
| Q41492958 | Aortic root dilatation and mitral valve prolapse in the fragile X syndrome |
| Q28274583 | Aortic root dilatation associated with partial trisomy 7(q31.2----qter) |
| Q33672810 | Ascertainment and severity of Marfan syndrome in a Scottish population |
| Q47779990 | Assessment of bone mineral density in adults and children with Marfan syndrome |
| Q48218491 | Assessment of the safety and efficacy of primary retropupillary fixation of iris-claw intraocular lenses in children with large lens subluxations. |
| Q30311161 | Auscultation of the Chest and Abdomen by Athletic Trainers |
| Q35194631 | Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes |
| Q70919575 | Basic Defects in the Marfan Syndrome |
| Q56654961 | Bilaterally painful anomalous insertion of the medial meniscus in a volleyball player with Marfanoid features |
| 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 |
| Q36823652 | Bone mineral density determinations by dual-energy x-ray absorptiometry in the management of patients with Marfan syndrome--some factors which affect the measurement |
| Q67772888 | Cardiac disease in pregnancy |
| Q30454633 | Cardiovascular magnetic resonance in Marfan syndrome |
| Q38215407 | Cardiovascular manifestations in Marfan syndrome and related diseases; multiple genes causing similar phenotypes |
| Q33612206 | Cardiovascular manifestations of Marfan's syndrome: improved evaluation by transoesophageal echocardiography |
| 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 |
| Q70697397 | Case report and study of collagen metabolism in Marfan's syndrome |
| Q72793557 | Case report: humero-spinal dysostosis |
| Q33677662 | Characterisation of four novel fibrillin-1 (FBN1) mutations in Marfan syndrome |
| Q73422108 | Characterization of microsatellite markers flanking FBN1: utility in the diagnostic evaluation for Marfan syndrome |
| Q37395189 | Collagenopathies-Implications for Abdominal Wall Reconstruction: A Systematic Review. |
| Q47228622 | Comprehensive molecular screening of the FBN1 gene favors locus homogeneity of classical Marfan syndrome |
| Q38057988 | Concomitant occurrence of hypohyperdontia in a patient with Marfan syndrome: a review of the literature and report of a case |
| Q33723361 | Congenital and idiopathic scoliosis: clinical and genetic aspects. |
| Q44495475 | Congenital aortic Regurgitation: Natural history and management |
| Q70691611 | Congenital contractural arachnodactyly, keratoconus, and probable Marfan syndrome in the same pedigree |
| Q56883352 | Congenital heart disease in pregnancy |
| Q41118476 | Consensus Document of the Italian Association of Hospital Cardiologists (ANMCO), Italian Society of Pediatric Cardiology (SICP), and Italian Society of Gynaecologists and Obstetrics (SIGO): pregnancy and congenital heart diseases |
| Q42965874 | Contractural arachnodactyly versus Marfan's syndrome |
| Q35197948 | Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families |
| Q34806881 | Current insights in diagnosis and management of the cardiovascular complications of Marfan's syndrome |
| Q36766898 | Current role of endovascular therapy in Marfan patients with previous aortic surgery |
| Q34145672 | Cysteine substitutions in epidermal growth factor-like domains of fibrillin-1: distinct effects on biochemical and clinical phenotypes |
| Q36209751 | Cystic lung in Marfan's syndrome |
| Q86525360 | Cystic medial necrosis and internal carotid artery dissection in a marfan sibling: Partial expression of marfan syndrome |
| Q35889608 | Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studies. |
| Q33874456 | De Novo Paternal FBN1 Mutation Detected in Embryos Before Implantation. |
| Q71708891 | Delineation of the Marfan phenotype associated with mutations in exons 23-32 of the FBN1 gene |
| Q38905858 | Descending aortic replacement after Nuss for pectus excavatum in a Marfan patient-Case report |
| Q67602977 | Detection of aortic dissection by magnetic resonance imaging in adults with Marfan's syndrome |
| Q40139533 | Diagnosis and management of Marfan syndrome |
| Q52862061 | Did the "Pigeon Chested Man" have Marfan's syndrome? |
| Q47117228 | Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome |
| Q42821154 | Dilatation of the great arteries in an infant with marfan syndrome and ventricular septal defect |
| Q35778595 | Disease-specific Growth Charts of Marfan Syndrome Patients in Korea |
| Q74651715 | Diseases of the aorta |
| Q36089996 | Dissecting aneurysm of aorta in rats fed with cysteamine |
| Q44227040 | Dissecting thoracic aortic aneurysm in a 22-year-old man. |
| Q41637847 | Dissection of the aorta: a clinical update |
| Q37462387 | Does altered aortic flow in marfan syndrome relate to aortic root dilatation? |
| Q35203225 | Duplication 9q34 syndrome |
| Q35247845 | Dural ectasia is a common feature of the Marfan syndrome. |
| Q70992170 | Early cardiac manifestations of Marfan's syndrome in the newborn |
| Q71218276 | Echocardiographic evaluation of aortic valve and root disease |
| Q41142505 | Echocardiographic evaluation of the aortic root and mitral valve in children and adolescents with isolated pectus excavatum: Comparison with Marfan patients |
| Q93617263 | Echocardiographic study of cardiac abnormalities in families of patients with Marfan's syndrome |
| Q30393311 | Economic and care considerations of Marfan syndrome |
| Q77808605 | Effect of long-term beta-blockade on aortic root compliance in patients with Marfan syndrome |
| Q33961346 | Elastic and collagenous networks in vascular diseases |
| Q33612201 | Elective replacement of the aortic root in Marfan's syndrome |
| Q36359995 | Elucidation of the gene defect in Marfan syndrome. Success by two complementary research strategies |
| Q33762331 | Epidural Anesthesia for Cesarean Section in a Pregnant Woman with Marfan Syndrome and Dural Ectasia. |
| Q47138067 | Etiology and pathogenesis of the Marfan syndrome: current understanding |
| Q45748472 | Evidence for Marfan cardiomyopathy |
| Q35254122 | Evolving phenotype of Marfan's syndrome |
| Q33674440 | Exclusion of the alpha 2(I) and alpha 1(III) collagen genes as the mutant loci in a Marfan syndrome family. |
| Q45125619 | Exogenous activation of BMP-2 signaling overcomes TGFβ-mediated inhibition of osteogenesis in Marfan embryonic stem cells and Marfan patient-specific induced pluripotent stem cells. |
| Q34203531 | Expression of a mutant human fibrillin allele upon a normal human or murine genetic background recapitulates a Marfan cellular phenotype |
| Q77953376 | Extensive aortic reconstruction for aortic aneurysms in Marfan syndrome |
| Q73969599 | FBN1 exon 2 splicing error in a patient with Marfan syndrome |
| Q67930772 | Familial Multiple Bilateral Pneumothorax Associated with Marfan Syndrome |
| Q69043999 | Familial spontaneous pneumothorax |
| Q59337327 | Family-based whole-exome sequencing identifies novel loss-of-function mutations of for Marfan syndrome |
| Q41812065 | Fibrillin and the eye. |
| Q35829553 | First genetic analysis of aneurysm genes in familial and sporadic abdominal aortic aneurysm |
| Q35011911 | Gene expression in acute Stanford type A dissection: a comparative microarray study |
| Q37413815 | Genetic alterations in syndromes with oral manifestations |
| Q24310509 | Genetic analysis of structural elastic fiber and collagen genes in familial adolescent idiopathic scoliosis |
| Q33676661 | Genetic markers on chromosome 7. |
| Q91577853 | Genetics of Thoracic and Abdominal Aortic Diseases |
| Q38601760 | Genetics of hereditary large vessel diseases |
| Q88361421 | Genetics of the extracellular matrix in aortic aneurysmal diseases |
| Q26828019 | Genetics of thoracic aortic aneurysm: at the crossroad of transforming growth factor-β signaling and vascular smooth muscle cell contractility |
| Q37381340 | Genomic mapping and how it has progressed |
| Q33839940 | Giant congenital aortic aneurysm with cleft sternum, supraumbilical raphé, and hemangiomatosis: report and review |
| Q78010930 | Growth and maturation in Marfan syndrome |
| Q47911657 | Health-related quality of life is unimpaired in children and adolescents with Marfan syndrome despite its distinctive phenotype |
| Q33173249 | Heart Block in Marfan's Syndrome |
| Q58071857 | Heterogeneous aortic response to acute β-adrenergic blockade in Marfan syndrome |
| Q73906766 | Hiatus/paraesophageal hernias in neonatal Marfan syndrome |
| Q33671324 | Homozygosity for autosomal dominant Marfan syndrome |
| Q34579168 | Host susceptibility factors in mycobacterial infection. Genetics and body morphotype |
| Q30443053 | Hypercoagulability in a patient with Marfan syndrome |
| Q53098426 | Imaging findings in a distinct lethal inherited arteriopathy syndrome associated with a novel mutation in the FBLN4 gene. |
| Q73283061 | Immunohistochemical abnormalities of fibrillin in cardiovascular tissues in Marfan's syndrome |
| Q85541071 | Impact of age and gender on cardiac pathology in children and adolescents with Marfan syndrome |
| Q69011172 | Increased aortic root stiffness associated with osteogenesis imperfecta |
| Q33382672 | Inherited bleeding disorders |
| Q47701145 | Insight into the molecular genetics of myopia |
| Q64964644 | Interventional repair of a vascular aneurysm in a patient with Marfan syndrome. |
| Q48620633 | Intracranial aneurysms in Marfan's syndrome: an autopsy study |
| Q73317456 | Iridocorneal adhesions in patients with the Marfan syndrome |
| Q38989610 | Is the benign joint hypermobility syndrome benign? |
| Q39590016 | Isolated external iliac artery aneurysm secondary to cystic medial necrosis |
| Q70140172 | Length polymorphism in the pro alpha 2(I) collagen gene: an alternative explanation in a case of Marfan syndrome |
| Q57222332 | Life expectancy in the Marfan syndrome |
| Q33597166 | Linkage analysis in Marfan syndrome |
| Q33597154 | Linkage analysis of five fibrillar collagen loci in a large French Marfan syndrome family |
| Q74705142 | Long-term prognosis of surgically-treated aortic aneurysms and dissections in patients with and without Marfan syndrome |
| Q71768663 | Lumbar spine in Marfan syndrome |
| Q82438067 | Lumbar spine mobility in Marfan syndrome. A clinical and radiological study |
| Q92027438 | Lung Function Changes are More Common in Marfan Patients Who Need Major Thoracic Surgery |
| Q44442499 | Magnetic resonance imaging of the main pulmonary artery: reliable assessment of dimensions in Marfan patients on a simple axial spin echo image |
| Q77315858 | Management of the patient with aortic root disease and aortic insufficiency |
| Q41435213 | Marfan Syndrome: Exclusion of genetic linkage to three major collagen genes |
| Q35602882 | Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin gene |
| Q72999813 | Marfan syndrome |
| Q36681743 | Marfan syndrome affecting four generations of a family without ocular involvement |
| Q35931816 | Marfan syndrome and pregnancy - a district hospital perspective |
| Q54329837 | Marfan syndrome as a paradigm for transcript-targeted preimplantation diagnosis of heterozygous mutations. |
| Q55671357 | Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene |
| Q47911572 | Marfan syndrome diagnosed in patients 32 years of age or older |
| 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 |
| 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. |
| Q37516648 | Marfan syndrome is closely linked to a marker on chromosome 15q1.5----q2.1. |
| Q64041313 | Marfan syndrome with type 2 diabetes mellitus: A case report from China |
| Q33677345 | Marfan syndrome. |
| Q36988542 | Marfan syndrome. Demonstration of abnormal elastin in aorta |
| Q50552464 | Marfan syndrome. What you need to know. |
| Q41636956 | Marfan syndrome: a mystery solved |
| 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 |
| Q34579317 | Marfan syndrome: clinical diagnosis and management |
| Q35596012 | Marfan syndrome: defective synthesis, secretion, and extracellular matrix formation of fibrillin by cultured dermal fibroblasts |
| Q43145462 | Marfan syndrome: light at the end of the tunnel? |
| Q35196800 | Marfan syndrome: no evidence for heterogeneity in different populations, and more precise mapping of the gene |
| Q72595207 | Marfan syndrome: the variability and outcome of operative management |
| Q56655033 | Marfan's Syndrome: Detection and Management |
| Q37934129 | Marfan's syndrome and coarctation. Coincidence or association? A case report |
| Q34117824 | Marfan's syndrome and isolated aneurysm of the abdominal aorta |
| Q48127624 | Marfan's syndrome, recurrent complex partial status epilepticus and myoclonus: a case report. |
| Q71059688 | Marfan's syndrome. Broad spectral surgical treatment cardiovascular manifestations |
| Q40356351 | Maternal and fetal complications of pregnancy in the Marfan syndrome |
| Q34347211 | Matrix metalloproteinases: from biology to therapeutic strategies in cardiovascular disease |
| Q33624374 | Metacarpal index in Marfan's syndrome and in constitutional tall stature |
| Q56336808 | Mitral valve prolapse |
| Q69059115 | Mitral valve prolapse |
| Q36756617 | Mitral valve prolapse associated with other disorders. Casual coincidence, common link, or fundamental genetic disturbance? |
| Q39603525 | Molecular and clinical aspects of connective tissue |
| Q35473537 | Muscle fibrillin deficiency in Marfan's syndrome myopathy |
| Q33634904 | Musculoskeletal rehabilitation and sports medicine. 4. Miscellaneous sports medicine topics |
| Q34337855 | Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome |
| Q47161617 | Natural history of aortic root aneurysms in Marfan syndrome. |
| Q45296303 | Nonsyndromic genetic predisposition to aortic dissection: a newly recognized, diagnosable, and preventable occurrence in families |
| Q73623267 | Novel approach to the molecular diagnosis of Marfan syndrome: application to sporadic cases and in prenatal diagnosis |
| Q69694840 | Nuclear magnetic resonance imaging in Marfan's syndrome |
| Q69917381 | Nuclear magnetic resonance imaging in the assessment of unusual abdominal aortic aneurysms |
| Q99239896 | Ocular Manifestations and Biometrics in Marfan's Syndrome from Eastern Nepal |
| Q49068532 | Ocular findings in 87 adults with Ghent-1 verified Marfan syndrome. |
| Q37512554 | Orthopaedic Aspects of Marfan Syndrome: The Experience of a Referral Center for Diagnosis of Rare Diseases. |
| Q69565305 | Osteogenesis imperfecta in childhood: cardiac and renal manifestations |
| Q36683618 | Osteoporosis and the Marfan syndrome |
| Q69386744 | Outcome of pectus excavatum in patients with Marfan syndrome and in the general population |
| Q41445276 | Overgrowth. Section V. Syndromes and other disorders associated with overgrowth |
| Q35765078 | Patterns of expression of fibrinolytic genes and matrix metalloproteinase-9 in dissecting aortic aneurysms |
| Q38859214 | Pectus excavatum: echocardiographic, pathophysiologic, and surgical insights |
| Q34267639 | Pneumothorax in the Marfan syndrome: prevalence and therapy |
| Q36181309 | Potential therapy paradigms for Marfan syndrome |
| Q35217097 | Pregnancy in women with Marfan's Syndrome |
| Q68428386 | Probable Homozygotic Form of the Marfan Syndrome in a Newborn Child |
| Q74653659 | Prognosis of Marfan and non-Marfan patients with cystic medial necrosis of the aorta |
| 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 |
| Q68261781 | Pulmonary emphysema in neonate with the Marfan syndrome |
| Q69242409 | Pulmonary hyperinflation and emphysema in infants with the Marfan syndrome |
| Q71956165 | Quantitation of fibrillin immunofluorescence in fibroblast cultures in the 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 |
| Q70684419 | Recreational and sports recommendations for the child with heart disease |
| Q28288147 | Recurrent ctb(7)(q31.3) and possible laminin involvement in a neonatal cutis laxa with a Marfan phenotype |
| Q48131167 | Regional anesthesia in Marfan syndrome, not all dural ectasias are the same: a report of two cases |
| Q55405162 | Renal autotransplantation for aortic dissection in Marfan's syndrome. |
| Q39515960 | Repeat Operation for Pseudoaneurysm of Left Ventricular Outflow in a Patient with Concomitant Takayasu's Arteritis and Marfan Syndrome |
| Q71983127 | Results of Cardiovascular Surgery in the Marfan Syndrome:A Retrospective Study of 49 Patients |
| Q41146847 | Retroperitoneal fibrosis in Marfan's syndrome |
| Q43530141 | Retrospective analysis of the effect of angiotensin II receptor blocker versus β-blocker on aortic root growth in paediatric patients with Marfan syndrome |
| Q40941475 | Role of echocardiography in perioperative management of patients undergoing open heart surgery |
| Q35199604 | Segregation of all four major fibrillar collagen genes in the Marfan syndrome. |
| Q35889026 | Severe neonatal Marfan syndrome resulting from a de novo 3-bp insertion into the fibrillin gene on chromosome 15. |
| Q44081831 | Severe periodontitis in Marfan's syndrome: a case report |
| Q39234167 | Sixteen-year experience with aortic root replacement. Results of 172 operations |
| Q35657562 | Skeletogenic phenotype of human Marfan embryonic stem cells faithfully phenocopied by patient-specific induced-pluripotent stem cells |
| Q48874340 | Sleep-disordered breathing in Marfan's syndrome. |
| Q33672767 | Sotos syndrome: a study of the diagnostic criteria and natural history |
| Q71221301 | Spinal deformity |
| Q33679253 | Spinal manifestations of skeletal dysplasias |
| Q70678281 | Spontaneous dissecting aneurysm of the ductus arteriosus in an infant with Marfan syndrome |
| Q45761532 | Stickler’s syndrome: review and differential diagnosis |
| Q43184222 | Successful management of a patient with Marfan syndrome complicated with acute aortic dissection using landiolol during Cesarean section. |
| Q74805152 | Successful treatment in a patient with Takayasu's arteritis and Marfan syndrome |
| Q68161441 | Sudden Unexpected Death in Sports |
| Q41790646 | Surgical approach for Stanford type A aortic dissection in a patient with Marfan syndrome and pectus excavatum |
| Q68050074 | Surgical management of children and young adults with Marfan syndrome and pectus excavatum |
| Q74842813 | Surgical management of mitral regurgitation associated with Marfan's syndrome |
| Q35565917 | Survival and complication free survival in Marfan's syndrome: implications of current guidelines |
| Q58613135 | Survival, causes of death, and cardiovascular events in patients with Marfan syndrome |
| Q46000642 | Suspected Marfan Syndrome in a Female Basketball Player. |
| Q36741640 | Systemic Diseases Affecting the Mesenteric Circulation |
| Q74410337 | The Marfan syndrome and pregnancy: a retrospective study in a Dutch population |
| Q68418659 | The Marfan syndrome--analysis of growth and cardiovascular manifestation |
| Q70190054 | The Marfan syndrome: abnormal aortic elastic properties |
| Q70878638 | The Wagner-Stickler syndrome: A study of 22 families |
| Q34211973 | The eye in the Marfan syndrome |
| Q33789095 | The genetic basis of aortic disease. Marfan syndrome and beyond |
| Q40405120 | The genetic basis of paediatric heart disease |
| Q36938716 | The genetics of mitral valve prolapse |
| Q34328604 | The inheritance of groin hernia: a systematic review |
| Q46076605 | The metacarpal index--obsolete in Marfan syndrome! |
| Q71063189 | The roving aorta of Marfan's syndrome: A case report |
| Q68072700 | Thoracoabdominal aortic aneurysm associated with Marfan's syndrome--report of a case |
| Q73593148 | Three-channeled aortic dissection in Marfan syndrome |
| Q39458507 | Total intravenous anaesthesia for caesarean section in a patient with Marfan's syndrome |
| Q45889714 | Towards an RNA-based therapy for Marfan syndrome |
| Q24614605 | Treatment guidelines for thoracic aortic aneurysms and dissections based on the underlying causative gene |
| Q37084846 | Two mutations in Marfan syndrome resulting in truncated fibrillin polypeptides |
| Q48240728 | Type A aortic dissection during late pregnancy in a patient with Marfan syndrome. |
| Q35197984 | Unilateral microfibrillar abnormalities in a case of asymmetric Marfan syndrome |
| Q82470846 | Urinary incontinence should be added to the manifestation in women with Marfan syndrome |
| Q38248889 | Use of genetics for personalized management of heritable thoracic aortic disease: how do we get there? |
| Q89417017 | Utility of serial 12-lead electrocardiograms in children with Marfan syndrome |
| Q52960621 | [Marfan syndrome and valvular disease]. |
| Q69534011 | [Marfan syndrome. A contribution to forensic medicine cases] |
| Q68974837 | [Marfan's or Marfan-like syndrome: value of echocardiography] |
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