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Archives Des Maladies Du Coeur Et Des Vaisseaux|June 25, 2004

[Neonatal forms of congenital long QT syndrome]J M Lupoglazoff, I Denjoy, E Villain, et al.

European Journal of Endocrinology|June 24, 2006

Increased adiponectin receptor-1 expression in adipose tissue of impaired glucose-tolerant obese subjects during weight lossM J Kim, M Maachi, C Debard, et al.

Journal of Medical Genetics|February 9, 2000

First description of germline mosaicism in familial hypertrophic cardiomyopathyJ F Forissier, P Richard, S Briault, et al.

Journal of Medical Genetics|October 4, 2002

Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experienceP Charron, D Héron, M Gargiulo, 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 Biologie Clinique|June 14, 2005

[Results transferability on RXL, ARX, X-Pand, BN2 (Dade Behring) and modular DP (Roche Diagnostics) analysers: application to component assays of fibrotest and Actitest]F Imbert-Bismut, D Messous, A Raoult, et al.

Journal of Medical Genetics|July 29, 1999

Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathyP Richard, R Isnard, L Carrier, et al.

Circulation Research|February 19, 1999

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndromeN Neyroud, P Richard, N Vignier, 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.

Heart (British Cardiac Society)|March 8, 2011

Plakophilin 2A is the dominant isoform in human heart tissue: consequences for the genetic screening of arrhythmogenic right ventricular cardiomyopathyE Gandjbakhch, P Charron, V Fressart, et al.

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Showing results (41-50 of 62) with videos related to

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Pageof 7

Archives Des Maladies Du Coeur Et Des Vaisseaux|June 25, 2004

[Neonatal forms of congenital long QT syndrome]J M Lupoglazoff, I Denjoy, E Villain, et al.

European Journal of Endocrinology|June 24, 2006

Increased adiponectin receptor-1 expression in adipose tissue of impaired glucose-tolerant obese subjects during weight lossM J Kim, M Maachi, C Debard, et al.

Journal of Medical Genetics|February 9, 2000

First description of germline mosaicism in familial hypertrophic cardiomyopathyJ F Forissier, P Richard, S Briault, et al.

Journal of Medical Genetics|October 4, 2002

Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experienceP Charron, D Héron, M Gargiulo, 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 Biologie Clinique|June 14, 2005

[Results transferability on RXL, ARX, X-Pand, BN2 (Dade Behring) and modular DP (Roche Diagnostics) analysers: application to component assays of fibrotest and Actitest]F Imbert-Bismut, D Messous, A Raoult, et al.

Journal of Medical Genetics|July 29, 1999

Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathyP Richard, R Isnard, L Carrier, et al.

Circulation Research|February 19, 1999

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndromeN Neyroud, P Richard, N Vignier, 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.

Heart (British Cardiac Society)|March 8, 2011

Plakophilin 2A is the dominant isoform in human heart tissue: consequences for the genetic screening of arrhythmogenic right ventricular cardiomyopathyE Gandjbakhch, P Charron, V Fressart, et al.

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