Villard E - Search Results

1

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

2

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

3

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: villard e. 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.

4

[Genetics and dilated cardiomyopathy].

Villard E. Villard E. Arch Mal Coeur Vaiss. 2003 Nov;96(11):1049-53. Arch Mal Coeur Vaiss. 2003. PMID: 14694780 Review. French.

5

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.

6

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.

7

A mutation in the drug transporter gene ABCC2 associated with impaired methotrexate elimination.

Hulot JS, Villard E, Maguy A, Morel V, Mir L, Tostivint I, William-Faltaos D, Fernandez C, Hatem S, Deray G, Komajda M, Leblond V, Lechat P. Hulot JS, et al. Among authors: villard e. Pharmacogenet Genomics. 2005 May;15(5):277-85. doi: 10.1097/01213011-200505000-00002. Pharmacogenet Genomics. 2005. PMID: 15864128

8

[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.

9

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

10

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

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