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Page 1
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
Genotype-phenotype analysis in four families with mutations in beta-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy.
Tesson F, Richard P, Charron P, Mathieu B, Cruaud C, Carrier L, Dubourg O, Lautié N, Desnos M, Millaire A, Isnard R, Hagege AA, Bouhour JB, Bennaceur M, Hainque B, Guicheney P, Schwartz K, Komajda M. Tesson F, et al. Hum Mutat. 1998;12(6):385-92. doi: 10.1002/(SICI)1098-1004(1998)12:6<385::AID-HUMU4>3.0.CO;2-E. Hum Mutat. 1998. PMID: 9829907
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.
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.
72 results