Millaire A - Search Results

1

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: millaire a. Circulation. 2003 May 6;107(17):2227-32. doi: 10.1161/01.CIR.0000066323.15244.54. Epub 2003 Apr 21. Circulation. 2003. PMID: 12707239

2

Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy.

Forissier JF, Carrier L, Farza H, Bonne G, Bercovici J, Richard P, Hainque B, Townsend PJ, Yacoub MH, Fauré S, Dubourg O, Millaire A, Hagège AA, Desnos M, Komajda M, Schwartz K. Forissier JF, et al. Among authors: millaire a. Circulation. 1996 Dec 15;94(12):3069-73. doi: 10.1161/01.cir.94.12.3069. Circulation. 1996. PMID: 8989109

3

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population.

Charron P, Dubourg O, Desnos M, Isnard R, Hagege A, Millaire A, Carrier L, Bonne G, Tesson F, Richard P, Bouhour JB, Schwartz K, Komajda M. Charron P, et al. Among authors: millaire a. Circulation. 1997 Jul 1;96(1):214-9. doi: 10.1161/01.cir.96.1.214. Circulation. 1997. PMID: 9236436

4

Genotype-phenotype analysis in four families with mutations in beta-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy.

Tesson F, Richard P, Charron P, Mathieu B, Cruaud C, Carrier L, Dubourg O, Lautié N, Desnos M, Millaire A, Isnard R, Hagege AA, Bouhour JB, Bennaceur M, Hainque B, Guicheney P, Schwartz K, Komajda M. Tesson F, et al. Among authors: millaire a. Hum Mutat. 1998;12(6):385-92. doi: 10.1002/(SICI)1098-1004(1998)12:6<385::AID-HUMU4>3.0.CO;2-E. Hum Mutat. 1998. PMID: 9829907

5

Doppler echocardiography in familial hypertrophic cardiomyopathy: the French Cooperative Study.

Dubourg O, Isnard R, Hagège A, Jondeau G, Desnos M, Sacrez A, Bouhour JB, Messner Pellenc P, Millaire A, Fetler L, et al. Dubourg O, et al. Among authors: millaire a. Echocardiography. 1995 May;12(3):235-41. doi: 10.1111/j.1540-8175.1995.tb00544.x. Echocardiography. 1995. PMID: 10150472

6

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: millaire a. Cardiovasc Res. 2008 Jan;77(1):118-25. doi: 10.1093/cvr/cvm015. Epub 2007 Sep 19. Cardiovasc Res. 2008. PMID: 18006477

7

[Clinico-pathological polymorphism of hypertrophic cardiomyopathy in echocardiography].

Dubourg O, Isnard R, Fetler L, Hagège A, Messner-Pellenc P, Desnos M, Millaire A, Sacrez A, Bouhour JB, Laurent M, et al. Dubourg O, et al. Among authors: millaire a. Arch Mal Coeur Vaiss. 1995 Apr;88(4 Suppl):563-7. Arch Mal Coeur Vaiss. 1995. PMID: 7487300 Clinical Trial. French.

8

[French familial multicenter survey of hypertrophic cardiomyopathy. Initial Doppler echocardiographic results].

Dubourg O, Komajda M, Isnard R, Hagège A, Desnos M, Sacrez A, Bouhour JB, Ferrière M, Millaire A, Jondeau G, et al. Dubourg O, et al. Among authors: millaire a. Arch Mal Coeur Vaiss. 1993 Feb;86 Spec No 2:59-64. Arch Mal Coeur Vaiss. 1993. PMID: 8215792 Clinical Trial. French.

9

Lack of association between polymorphisms of eight candidate genes and idiopathic dilated cardiomyopathy: the CARDIGENE study.

Tiret L, Mallet C, Poirier O, Nicaud V, Millaire A, Bouhour JB, Roizès G, Desnos M, Dorent R, Schwartz K, Cambien F, Komajda M. Tiret L, et al. Among authors: millaire a. J Am Coll Cardiol. 2000 Jan;35(1):29-35. doi: 10.1016/s0735-1097(99)00522-7. J Am Coll Cardiol. 2000. PMID: 10636255 Free article.

10

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: millaire a. 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.

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