Charron P - Search Results

1

Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases.

Pinto YM, Elliott PM, Arbustini E, Adler Y, Anastasakis A, Böhm M, Duboc D, Gimeno J, de Groote P, Imazio M, Heymans S, Klingel K, Komajda M, Limongelli G, Linhart A, Mogensen J, Moon J, Pieper PG, Seferovic PM, Schueler S, Zamorano JL, Caforio AL, Charron P. Pinto YM, et al. Among authors: charron p. Eur Heart J. 2016 Jun 14;37(23):1850-8. doi: 10.1093/eurheartj/ehv727. Epub 2016 Jan 19. Eur Heart J. 2016. PMID: 26792875 Review.

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

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

5

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

6

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

7

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

8

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.

9

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

10

Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases.

Elliott P, Andersson B, Arbustini E, Bilinska Z, Cecchi F, Charron P, Dubourg O, Kühl U, Maisch B, McKenna WJ, Monserrat L, Pankuweit S, Rapezzi C, Seferovic P, Tavazzi L, Keren A. Elliott P, et al. Among authors: charron p. Eur Heart J. 2008 Jan;29(2):270-6. doi: 10.1093/eurheartj/ehm342. Epub 2007 Oct 4. Eur Heart J. 2008. PMID: 17916581

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