Villard E - Search Results

1

Involvement of BAG3 and HSPB7 loci in various etiologies of systolic heart failure: Results of a European collaboration assembling more than 2000 patients.

Garnier S, Hengstenberg C, Lamblin N, Dubourg O, De Groote P, Fauchier L, Trochu JN, Arbustini E, Esslinger U, Barton PJ, Meder B, Katus H, Frese K, Komajda M, Cook SA, Isnard R, Tiret L, Villard E, Charron P. Garnier S, et al. Among authors: villard e. Int J Cardiol. 2015;189:105-7. doi: 10.1016/j.ijcard.2015.04.003. Epub 2015 Apr 1. Int J Cardiol. 2015. PMID: 25889438 Free article. No abstract available.

2

Identification of new polymorphisms of the angiotensin I-converting enzyme (ACE) gene, and study of their relationship to plasma ACE levels by two-QTL segregation-linkage analysis.

Villard E, Tiret L, Visvikis S, Rakotovao R, Cambien F, Soubrier F. Villard E, et al. Am J Hum Genet. 1996 Jun;58(6):1268-78. Am J Hum Genet. 1996. PMID: 8651305 Free PMC article.

3

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: villard e. 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

4

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

5

Charcot-Marie-Tooth features and maculopathy in a patient with Danon disease.

Laforêt P, Charron P, Maisonobe T, Romero NB, Villard E, Sebillon P, Drouin-Garraud V, Dubourg O, Fardeau M, Komajda M, Eymard B. Laforêt P, et al. Among authors: villard e. Neurology. 2004 Oct 26;63(8):1535. doi: 10.1212/01.wnl.0000141858.80738.aa. Neurology. 2004. PMID: 15505188 No abstract available.

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. 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

[Review: genetics of familial dilated cardiomyopathy].

Amara ME, Villard E, Komajda M. Amara ME, et al. Among authors: villard e. Ann Cardiol Angeiol (Paris). 2005 Jun;54(3):151-6. doi: 10.1016/j.ancard.2004.09.005. Ann Cardiol Angeiol (Paris). 2005. PMID: 15991472 Review. French.

8

Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy.

Duboscq-Bidot L, Xu P, Charron P, Neyroud N, Dilanian G, Millaire A, Bors V, Komajda M, Villard E. Duboscq-Bidot L, et al. Among authors: villard e. Cardiovasc Res. 2008 Jan;77(1):118-25. doi: 10.1093/cvr/cvm015. Epub 2007 Sep 19. Cardiovasc Res. 2008. PMID: 18006477

9

Sporadic arrhythmogenic right ventricular cardiomyopathy/dysplasia due to a de novo mutation.

Gandjbakhch E, Fressart V, Bertaux G, Faivre L, Simon F, Frank R, Fontaine G, Villard E, Coirault C, Hainque B, Charron P. Gandjbakhch E, et al. Among authors: villard e. Europace. 2009 Mar;11(3):379-81. doi: 10.1093/europace/eun378. Epub 2009 Jan 16. Europace. 2009. PMID: 19151369

10

Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy.

Duboscq-Bidot L, Charron P, Ruppert V, Fauchier L, Richter A, Tavazzi L, Arbustini E, Wichter T, Maisch B, Komajda M, Isnard R, Villard E; EUROGENE Heart Failure Network. Duboscq-Bidot L, et al. Among authors: villard e. Eur Heart J. 2009 Sep;30(17):2128-36. doi: 10.1093/eurheartj/ehp225. Epub 2009 Jun 12. Eur Heart J. 2009. PMID: 19525294

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