Richard P - Search Results

1

Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic survey.

Charron P, Villard E, Sébillon P, Laforêt P, Maisonobe T, Duboscq-Bidot L, Romero N, Drouin-Garraud V, Frébourg T, Richard P, Eymard B, Komajda M. Charron P, et al. Among authors: richard p. Heart. 2004 Aug;90(8):842-6. doi: 10.1136/hrt.2003.029504. Heart. 2004. PMID: 15253947 Free PMC article.

2

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children.

Charron P, Dubourg O, Desnos M, Bouhour JB, Isnard R, Hagege A, Carrier L, Bonne G, Tesson F, Richard P, Hainque B, Schwartz K, Komajda M. Charron P, et al. Among authors: richard p. Eur Heart J. 1998 Sep;19(9):1377-82. doi: 10.1053/euhj.1998.1049. Eur Heart J. 1998. PMID: 9792264 Clinical Trial.

3

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: richard p. Genet Couns. 1997;8(2):107-14. Genet Couns. 1997. PMID: 9219008

4

Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy.

Flavigny J, Richard P, Isnard R, Carrier L, Charron P, Bonne G, Forissier JF, Desnos M, Dubourg O, Komajda M, Schwartz K, Hainque B. Flavigny J, et al. Among authors: richard p. J Mol Med (Berl). 1998 Mar;76(3-4):208-14. doi: 10.1007/s001090050210. J Mol Med (Berl). 1998. PMID: 9535554

5

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. Among authors: richard p. 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

6

Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy.

Richard P, Isnard R, Carrier L, Dubourg O, Donatien Y, Mathieu B, Bonne G, Gary F, Charron P, Hagege M, Komajda M, Schwartz K, Hainque B. Richard P, et al. J Med Genet. 1999 Jul;36(7):542-5. J Med Genet. 1999. PMID: 10424815 Free PMC article.

7

Homozygotes for a R869G mutation in the beta -myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathy.

Richard P, Charron P, Leclercq C, Ledeuil C, Carrier L, Dubourg O, Desnos M, Bouhour JB, Schwartz K, Daubert JC, Komajda M, Hainque B. Richard P, et al. J Mol Cell Cardiol. 2000 Aug;32(8):1575-83. doi: 10.1006/jmcc.2000.1193. J Mol Cell Cardiol. 2000. PMID: 10900182

8

Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience.

Charron P, Héron D, Gargiulo M, Richard P, Dubourg O, Desnos M, Bouhour JB, Feingold J, Carrier L, Hainque B, Schwartz K, Komajda M. Charron P, et al. Among authors: richard p. J Med Genet. 2002 Oct;39(10):741-6. doi: 10.1136/jmg.39.10.741. J Med Genet. 2002. PMID: 12362031 Free PMC article.

9

Accuracy of European diagnostic criteria for familial hypertrophic cardiomyopathy in a genotyped population.

Charron P, Forissier JF, Amara ME, Dubourg O, Desnos M, Bouhour JB, Isnard R, Hagege A, Bénaïche A, Richard P, Schwartz K, Komajda M. Charron P, et al. Among authors: richard p. Int J Cardiol. 2003 Jul;90(1):33-8; discussion 38-40. doi: 10.1016/s0167-5273(02)00534-x. Int J Cardiol. 2003. PMID: 12821216

10

[Diagnostic value of a two-dimensional echocardiographic score for left ventricular hypertrophy validated by the Imatron CT scan in familial hypertrophic cardiomyopathy].

Forissier JF, Charron P, du Montcel ST, Hagège A, Richard P, Desnos M, Schwartz K, Mousseaux E, Komajda M, Dubourg O. Forissier JF, et al. Among authors: richard p. Arch Mal Coeur Vaiss. 2006 Oct;99(10):877-82. Arch Mal Coeur Vaiss. 2006. PMID: 17100137 French.

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