Mitral valve dysfunction in the Marfan syndrome. Clinical and echocardiographic study of prevalence and natural history

scientific article published on 01 May 1983

Mitral valve dysfunction in the Marfan syndrome. Clinical and echocardiographic study of prevalence and natural history is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/0002-9343(83)91070-7
P698PubMed publication ID6837604

P2093author name stringR E Pyeritz
M A Wappel
P433issue5
P304page(s)797-807
P577publication date1983-05-01
P1433published inAmerican Journal of MedicineQ2842959
P1476titleMitral valve dysfunction in the Marfan syndrome. Clinical and echocardiographic study of prevalence and natural history
P478volume74

Reverse relations

cites work (P2860)
Q42431508A case of Marfan syndrome with acute monoblastic leukemia
Q49822666Anomalous Coronary Artery Origin in a Young Patient with Marfan Syndrome.
Q40165357Associations of Age and Sex With Marfan Phenotype: The National Heart, Lung, and Blood Institute GenTAC (Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions) Registry
Q36824423Cardiac anomalies complicating congenital contractural arachnodactyly
Q92218873Cardiovascular Management of Adults with Marfan Syndrome
Q33612206Cardiovascular manifestations of Marfan's syndrome: improved evaluation by transoesophageal echocardiography
Q34806881Current insights in diagnosis and management of the cardiovascular complications of Marfan's syndrome
Q62607051Diastolic subclinical primary alterations in marfan syndrome and marfan-related disorders
Q92994244Differences in Cardiovascular Manifestation of Marfan Syndrome Between Children and Adults
Q93617263Echocardiographic study of cardiac abnormalities in families of patients with Marfan's syndrome
Q36638702Genetic association analyses highlight biological pathways underlying mitral valve prolapse
Q35651899Identification of defects in the fibrillin gene and protein in individuals with the Marfan syndrome and related disorders
Q36660642Infantile Marfan syndrome in a Korean tertiary referral center
Q49369869Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse
Q34384658Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28.
Q33677345Marfan syndrome.
Q26747739Marfan syndrome: current perspectives
Q24553344Marfan's syndrome
Q30482248Marfan's syndrome and the heart.
Q39828386Minimally invasive cardiac surgery for a young woman with Marfan syndrome and mitral regurgitation
Q37922113Mitral valve disease in Marfan syndrome and related disorders.
Q26781699Mitral valve disease--morphology and mechanisms
Q24802228Mitral valve prolapse associated with celiac artery stenosis: a new ultrasonographic syndrome?
Q33931523Natural history of cardiovascular manifestations in Marfan syndrome
Q56988790Novel exon skipping mutation in the fibrillin-1 gene: Two 'hot spots' for the neonatal Marfan syndrome
Q38639475Overview of current surgical strategies for aortic disease in patients with Marfan syndrome
Q26864278Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome
Q77178218Reduced penetrance and variable expressivity of familial thoracic aortic aneurysms/dissections
Q71244153Spectrum of structural abnormalities in floppy mitral valve echocardiographic evaluation
Q35099493Surgical Management of Mitral Regurgitation in Patients with Marfan Syndrome during Infancy and Early Childhood
Q74842813Surgical management of mitral regurgitation associated with Marfan's syndrome
Q44661801Surgical treatment of cardiovascular manifestations of Marfan's syndrome
Q68418659The Marfan syndrome--analysis of growth and cardiovascular manifestation
Q64063306The Potential Beneficial Effects of Resveratrol on Cardiovascular Complications in Marfan Syndrome Patients⁻Insights from Rodent-Based Animal Studies
Q37041270Valvular Emergencies
Q52960621[Marfan syndrome and valvular disease].

Search more.