New concepts in hypertrophic cardiomyopathies, part I.
- 23 October 2001
- journal article
- review article
- Published by Wolters Kluwer Health in Circulation
- Vol. 104 (17) , 2113-2116
- https://doi.org/10.1161/hc4201.097429
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Hypertrophic Cardiomyopathy Caused by a Novel α-Tropomyosin Mutation (V95A) Is Associated With Mild Cardiac Phenotype, Abnormal Calcium Binding to Troponin, Abnormal Myosin Cycling, and Poor PrognosisCirculation, 2001
- Sudden death in hypertrophic cardiomyopathy: identification of high risk patientsPublished by Elsevier ,2000
- Molecular Genetic Basis of Hypertrophic Cardiomyopathy:Journal of Cardiovascular Electrophysiology, 1998
- Sudden Death in Young Competitive AthletesJAMA, 1996
- A Mouse Model of Familial Hypertrophic CardiomyopathyScience, 1996
- Detection of a new mutation in the beta-myosin heavy chain gene in an individual with hypertrophic cardiomyopathy.Journal of Clinical Investigation, 1992
- A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutationPublished by Elsevier ,1990
- Syncope in hypertrophic cardiomyopathy: Multivariate analysis of prognostic determinantsJournal of the American College of Cardiology, 1990
- Hypertrophic CardiomyopathyNew England Journal of Medicine, 1987
- Hypertrophic cardiomyopathy. The importance of the site and the extent of hypertrophy. A reviewProgress in Cardiovascular Diseases, 1985