Charron P - Search Results

1

Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.

Sébillon P, Bouchier C, Bidot LD, Bonne G, Ahamed K, Charron P, Drouin-Garraud V, Millaire A, Desrumeaux G, Benaïche A, Charniot JC, Schwartz K, Villard E, Komajda M. Sébillon P, et al. Among authors: charron p. J Med Genet. 2003 Aug;40(8):560-7. doi: 10.1136/jmg.40.8.560. J Med Genet. 2003. PMID: 12920062 Free PMC article.

2

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. Among authors: charron p. J Med Genet. 1999 Jul;36(7):542-5. J Med Genet. 1999. PMID: 10424815 Free PMC article.

3

Epidemiology of desmin and cardiac actin gene mutations in a european population of dilated cardiomyopathy.

Tesson F, Sylvius N, Pilotto A, Dubosq-Bidot L, Peuchmaurd M, Bouchier C, Benaiche A, Mangin L, Charron P, Gavazzi A, Tavazzi L, Arbustini E, Komajda M. Tesson F, et al. Among authors: charron p. Eur Heart J. 2000 Nov;21(22):1872-6. doi: 10.1053/euhj.2000.2245. Eur Heart J. 2000. PMID: 11052860

4

A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16.

Sylvius N, Tesson F, Gayet C, Charron P, Bénaïche A, Peuchmaurd M, Duboscq-Bidot L, Feingold J, Beckmann JS, Bouchier C, Komajda M. Sylvius N, et al. Among authors: charron p. Am J Hum Genet. 2001 Jan;68(1):241-6. doi: 10.1086/316929. Epub 2000 Nov 20. Am J Hum Genet. 2001. PMID: 11085912 Free PMC article.

5

[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.

6

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.

7

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. Heart. 2004 Aug;90(8):842-6. doi: 10.1136/hrt.2003.029504. Heart. 2004. PMID: 15253947 Free PMC article.

8

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

9

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

10

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

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