Family history of severe cardiovascular disease in Marfan syndrome is associated with increased aortic diameter and decreased survival
Open Access
- 1 October 1995
- journal article
- research article
- Published by Elsevier in Journal of the American College of Cardiology
- Vol. 26 (4), 1062-1067
- https://doi.org/10.1016/0735-1097(95)00258-0
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Life expectancy in the Marfan syndromeThe American Journal of Cardiology, 1995
- Current Diagnosis and Prescription for the Marian Syndrome: Aortic Root and Valve ReplacementJournal of Cardiac Surgery, 1994
- Prognostic significance of the pattern of aortic root dilation in the Marfan syndromeJournal of the American College of Cardiology, 1993
- Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin gene.Journal of Clinical Investigation, 1992
- Partial sequence of a candidate gene for the Marfan syndromeNature, 1991
- Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genesNature, 1991
- Two-dimensional echocardiographic aortic root dimensions in normal children and adultsThe American Journal of Cardiology, 1989
- The Marfan Syndrome: Diagnosis and ManagementNew England Journal of Medicine, 1979
- Aortic root dilatation and mitral valve prolapse in Marfan's syndrome: an ECHOCARDIOgraphic study.Circulation, 1975
- Maximum utilization of the life table method in analyzing survivalJournal of Chronic Diseases, 1958