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The Journal of Nutrition, Health & Aging|October 27, 2006
Management of heart failure in the elderly: recommendations from the French Society of Cardiology (SFC) and the French Society of Gerontology and Geriatrics (SFGG)M Komajda, O Hanon, J F Aupetit, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|June 1, 2006
Heart failure with preserved systolic function: a diagnostic algorithm for a pragmatic definitionY Juillière, J N Trochu, P de Groote, et al.European Heart Journal|October 29, 2000
Epidemiology of desmin and cardiac actin gene mutations in a european population of dilated cardiomyopathyF Tesson, N Sylvius, A Pilotto, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|January 1, 1983
[Long-term treatment of chronic heart failure by an inhibitor of angiotensin converting enzyme]M Komajda, M Eugène, J Evans, et al.Journal of Molecular and Cellular Cardiology|February 1, 1997
The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutationF Tesson, C Dufour, J C Moolman, et al.Journal of Molecular and Cellular Cardiology|May 25, 1999
Characterization of a unique genetic variant in the beta1-adrenoceptor gene and evaluation of its role in idiopathic dilated cardiomyopathy. CARDIGENE GroupF Tesson, P Charron, M Peuchmaurd, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Penetrance of familial hypertrophic cardiomyopathyP Charron, L Carrier, O Dubourg, et al.European Journal of Heart Failure|August 11, 2000
Familial dilated cardiomyopathy: clinical features in French familiesL Mangin, P Charron, F Tesson, et al.Journal of Medical Genetics|August 16, 2003
Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutationsP Sébillon, C Bouchier, L D Bidot, et al.Nature Genetics|December 1, 1995
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathyG Bonne, L Carrier, J Bercovici, et al.Pageof 36