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Characterization of a unique genetic variant in the beta1-adrenoceptor gene and evaluation of its role in idiopathic dilated cardiomyopathy. CARDIGENE Group.
Tesson F, Charron P, Peuchmaurd M, Nicaud V, Cambien F, Tiret L, Poirier O, Desnos M, Jullières Y, Amouyel P, Roizès G, Dorent R, Schwartz K, Komajda M. Tesson F, et al. J Mol Cell Cardiol. 1999 May;31(5):1025-32. doi: 10.1006/jmcc.1999.0947. J Mol Cell Cardiol. 1999. PMID: 10336842 Clinical Trial.
Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene. CARDIGENE group.
Charron P, Tesson F, Poirier O, Nicaud V, Peuchmaurd M, Tiret L, Cambien F, Amouyel P, Dubourg O, Bouhour J, Millaire A, Juilliere Y, Bareiss P, André-Fouët X, Pouillart F, Arveiler D, Ferrières J, Dorent R, Roizès G, Schwartz K, Desnos M, Komajda M. Charron P, et al. Among authors: tesson f. Eur Heart J. 1999 Nov;20(21):1587-91. doi: 10.1053/euhj.1999.1696. Eur Heart J. 1999. PMID: 10529327
Genetic aspects of heart failure.
Komajda M, Charron P, Tesson F. Komajda M, et al. Among authors: tesson f. Eur J Heart Fail. 1999 Jun;1(2):121-6. doi: 10.1016/s1388-9842(99)00026-4. Eur J Heart Fail. 1999. PMID: 10937920 Free article. Review.
Familial dilated cardiomyopathy: clinical features in French families.
Mangin L, Charron P, Tesson F, Mallet A, Dubourg O, Desnos M, Benaïsche A, Gayet C, Gibelin P, Davy JM, Bonnet J, Sidi D, Schwartz K, Komajda M. Mangin L, et al. Among authors: tesson f. Eur J Heart Fail. 1999 Dec;1(4):353-61. doi: 10.1016/s1388-9842(99)00047-1. Eur J Heart Fail. 1999. PMID: 10937948 Free article.
Penetrance of familial hypertrophic cardiomyopathy.
Charron P, Carrier L, Dubourg O, Tesson F, Desnos M, Richard P, Bonne G, Guicheney P, Hainque B, Bouhour JB, Mallet A, Feingold J, Schwartz K, Komajda M. Charron P, et al. Among authors: tesson f. Genet Couns. 1997;8(2):107-14. Genet Couns. 1997. PMID: 9219008
64 results