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M Desnos

Showing results (111-120 of 128) with videos related to

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Journal of the American College of Cardiology|January 15, 2000
Lack of association between polymorphisms of eight candidate genes and idiopathic dilated cardiomyopathy: the CARDIGENE studyL Tiret, C Mallet, O Poirier, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 16, 1998
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathyJ Flavigny, P Richard, R Isnard, et al.
Annales De Cardiologie Et D'Angeiologie|January 13, 2004
[Educating patients about heart failure in community hospitals: it is possible...]P Jourdain, F Funck, M Bellorini, et al.
Journal of Molecular and Cellular Cardiology|July 20, 2000
Homozygotes for a R869G mutation in the beta -myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathyP Richard, P Charron, C Leclercq, et al.
Circulation|July 1, 1997
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult populationP Charron, O Dubourg, M Desnos, et al.
European Heart Journal|October 29, 1998
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped childrenP Charron, O Dubourg, M Desnos, et al.
International Journal of Cardiology|June 25, 2003
Accuracy of European diagnostic criteria for familial hypertrophic cardiomyopathy in a genotyped populationP Charron, J F Forissier, M E Amara, et al.
European Heart Journal|March 21, 1998
Genotype-phenotype correlations in familial hypertrophic cardiomyopathy. A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genesP Charron, O Dubourg, M Desnos, 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.
European Journal of Heart Failure|August 11, 2000
Familial dilated cardiomyopathy: clinical features in French familiesL Mangin, P Charron, F Tesson, et al.
Pageof 13

Showing results (111-120 of 128) with videos related to

Sort By:
Pageof 13
Journal of the American College of Cardiology|January 15, 2000
Lack of association between polymorphisms of eight candidate genes and idiopathic dilated cardiomyopathy: the CARDIGENE studyL Tiret, C Mallet, O Poirier, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 16, 1998
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathyJ Flavigny, P Richard, R Isnard, et al.
Annales De Cardiologie Et D'Angeiologie|January 13, 2004
[Educating patients about heart failure in community hospitals: it is possible...]P Jourdain, F Funck, M Bellorini, et al.
Journal of Molecular and Cellular Cardiology|July 20, 2000
Homozygotes for a R869G mutation in the beta -myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathyP Richard, P Charron, C Leclercq, et al.
Circulation|July 1, 1997
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult populationP Charron, O Dubourg, M Desnos, et al.
European Heart Journal|October 29, 1998
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped childrenP Charron, O Dubourg, M Desnos, et al.
International Journal of Cardiology|June 25, 2003
Accuracy of European diagnostic criteria for familial hypertrophic cardiomyopathy in a genotyped populationP Charron, J F Forissier, M E Amara, et al.
European Heart Journal|March 21, 1998
Genotype-phenotype correlations in familial hypertrophic cardiomyopathy. A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genesP Charron, O Dubourg, M Desnos, 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.
European Journal of Heart Failure|August 11, 2000
Familial dilated cardiomyopathy: clinical features in French familiesL Mangin, P Charron, F Tesson, et al.
Pageof 13