Charron P - Search Results

1

A familial form of conduction defect related to a mutation in the PRKAG2 gene.

Charron P, Genest M, Richard P, Komajda M, Pochmalicki G. Charron P, et al. Europace. 2007 Aug;9(8):597-600. doi: 10.1093/europace/eum071. Epub 2007 May 4. Europace. 2007. PMID: 17483151

2

Genes and their polymorphisms in mono- and multifactorial cardiomyopathies: towards pharmacogenomics in heart failure.

Charron P, Komajda M. Charron P, et al. Pharmacogenomics. 2002 May;3(3):367-78. doi: 10.1517/14622416.3.3.367. Pharmacogenomics. 2002. PMID: 12052144 Review.

3

[Idiopathic cardiomyopathies].

Komajda M, Charron P. Komajda M, et al. Among authors: charron p. Rev Prat. 2002 Oct 1;52(15):1664-70. Rev Prat. 2002. PMID: 12434596 Review. French.

4

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.

Richard P, Charron P, Carrier L, Ledeuil C, Cheav T, Pichereau C, Benaiche A, Isnard R, Dubourg O, Burban M, Gueffet JP, Millaire A, Desnos M, Schwartz K, Hainque B, Komajda M; EUROGENE Heart Failure Project. Richard P, et al. Among authors: charron p. Circulation. 2003 May 6;107(17):2227-32. doi: 10.1161/01.CIR.0000066323.15244.54. Epub 2003 Apr 21. Circulation. 2003. PMID: 12707239

5

Mutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy.

Sylvius N, Duboscq-Bidot L, Bouchier C, Charron P, Benaiche A, Sébillon P, Komajda M, Villard E. Sylvius N, et al. Among authors: charron p. Am J Med Genet A. 2003 Jul 1;120A(1):8-12. doi: 10.1002/ajmg.a.20003. Am J Med Genet A. 2003. PMID: 12794684

6

Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first case.

Charron P, Héron D, Gargiulo M, Feingold J, Oury JF, Richard P, Komajda M. Charron P, et al. Prenat Diagn. 2004 Sep;24(9):701-3. doi: 10.1002/pd.969. Prenat Diagn. 2004. PMID: 15386449

7

Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene.

Villard E, Duboscq-Bidot L, Charron P, Benaiche A, Conraads V, Sylvius N, Komajda M. Villard E, et al. Among authors: charron p. Eur Heart J. 2005 Apr;26(8):794-803. doi: 10.1093/eurheartj/ehi193. Epub 2005 Mar 15. Eur Heart J. 2005. PMID: 15769782

8

Diagnostic accuracy of a 2D left ventricle hypertrophy score for familial hypertrophic cardiomyopathy.

Forissier JF, Charron P, Tezenas du Montcel S, Hagège A, Isnard R, Carrier L, Richard P, Desnos M, Bouhour JB, Schwartz K, Komajda M, Dubourg O. Forissier JF, et al. Among authors: charron p. Eur Heart J. 2005 Sep;26(18):1882-6. doi: 10.1093/eurheartj/ehi276. Epub 2005 Apr 28. Eur Heart J. 2005. PMID: 15860513

9

Molecular genetics in hypertrophic cardiomyopathy: towards individualized management of the disease.

Charron P, Komajda M. Charron P, et al. Expert Rev Mol Diagn. 2006 Jan;6(1):65-78. doi: 10.1586/14737159.6.1.65. Expert Rev Mol Diagn. 2006. PMID: 16359268 Review.

10

Novel Lamp-2 gene mutation and successful treatment with heart transplantation in a large family with Danon disease.

Echaniz-Laguna A, Mohr M, Epailly E, Nishino I, Charron P, Richard P, Guiraud-Chaumeil C, Tranchant C. Echaniz-Laguna A, et al. Among authors: charron p. Muscle Nerve. 2006 Mar;33(3):393-7. doi: 10.1002/mus.20471. Muscle Nerve. 2006. PMID: 16372318

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