Charron P - Search Results

1

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. 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

2

[Hypertrophic cardiomyopathies].

Charron P, Komajda M. Charron P, et al. Arch Mal Coeur Vaiss. 2003 Nov;96(11):1042-7. Arch Mal Coeur Vaiss. 2003. PMID: 14694779 Review. French.

3

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. 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.

4

[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: charron p. Arch Mal Coeur Vaiss. 2006 Oct;99(10):877-82. Arch Mal Coeur Vaiss. 2006. PMID: 17100137 French.

5

[Demonstration of a fifth locus implicated in familial hypertrophic cardiomyopathies].

Hengstenberg C, Charron P, Isnard R, Beckmann JS, Fetler L, Desnos M, Hagège A, Bouhour JB, Souriant G, Dubourg O, et al. Hengstenberg C, et al. Among authors: charron p. Arch Mal Coeur Vaiss. 1994 Dec;87(12):1655-62. Arch Mal Coeur Vaiss. 1994. PMID: 7786104 French.

6

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

7

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population.

Charron P, Dubourg O, Desnos M, Isnard R, Hagege A, Millaire A, Carrier L, Bonne G, Tesson F, Richard P, Bouhour JB, Schwartz K, Komajda M. Charron P, et al. Circulation. 1997 Jul 1;96(1):214-9. doi: 10.1161/01.cir.96.1.214. Circulation. 1997. PMID: 9236436

8

Genotype-phenotype correlations in familial hypertrophic cardiomyopathy. A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes.

Charron P, Dubourg O, Desnos M, Isnard R, Hagege A, Bonne G, Carrier L, Tesson F, Bouhour JB, Buzzi JC, Feingold J, Schwartz K, Komajda M. Charron P, et al. Eur Heart J. 1998 Jan;19(1):139-45. doi: 10.1053/euhj.1997.0575. Eur Heart J. 1998. PMID: 9503187

9

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: charron p. J Mol Med (Berl). 1998 Mar;76(3-4):208-14. doi: 10.1007/s001090050210. J Mol Med (Berl). 1998. PMID: 9535554

10

Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene.

Charron P, Dubourg O, Desnos M, Bennaceur M, Carrier L, Camproux AC, Isnard R, Hagege A, Langlard JM, Bonne G, Richard P, Hainque B, Bouhour JB, Schwartz K, Komajda M. Charron P, et al. Circulation. 1998 Jun 9;97(22):2230-6. doi: 10.1161/01.cir.97.22.2230. Circulation. 1998. PMID: 9631872

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