Bonne G - Search Results

1

Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy.

Friedrich FW, Wilding BR, Reischmann S, Crocini C, Lang P, Charron P, Müller OJ, McGrath MJ, Vollert I, Hansen A, Linke WA, Hengstenberg C, Bonne G, Morner S, Wichter T, Madeira H, Arbustini E, Eschenhagen T, Mitchell CA, Isnard R, Carrier L. Friedrich FW, et al. Among authors: bonne g. Hum Mol Genet. 2012 Jul 15;21(14):3237-54. doi: 10.1093/hmg/dds157. Epub 2012 Apr 20. Hum Mol Genet. 2012. PMID: 22523091

2

The COX8 gene is not the disease gene of the CMH4 locus in familial hypertrophic cardiomyopathy.

Bonne G, Carrier L, Schwartz K, Komajda M. Bonne G, et al. J Med Genet. 1995 Aug;32(8):670-1. doi: 10.1136/jmg.32.8.670. J Med Genet. 1995. PMID: 7473670 Free PMC article. No abstract available.

3

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy.

Bonne G, Carrier L, Bercovici J, Cruaud C, Richard P, Hainque B, Gautel M, Labeit S, James M, Beckmann J, Weissenbach J, Vosberg HP, Fiszman M, Komajda M, Schwartz K. Bonne G, et al. Nat Genet. 1995 Dec;11(4):438-40. doi: 10.1038/ng1295-438. Nat Genet. 1995. PMID: 7493026

4

Penetrance of familial hypertrophic cardiomyopathy.

Charron P, Carrier L, Dubourg O, Tesson F, Desnos M, Richard P, Bonne G, Guicheney P, Hainque B, Bouhour JB, Mallet A, Feingold J, Schwartz K, Komajda M. Charron P, et al. Among authors: bonne g. Genet Couns. 1997;8(2):107-14. Genet Couns. 1997. PMID: 9219008

5

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: bonne g. Circulation. 1997 Jul 1;96(1):214-9. doi: 10.1161/01.cir.96.1.214. Circulation. 1997. PMID: 9236436

6

Genotype-phenotype correlations in familial hypertrophic cardiomyopathy. A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes.

Charron P, Dubourg O, Desnos M, Isnard R, Hagege A, Bonne G, Carrier L, Tesson F, Bouhour JB, Buzzi JC, Feingold J, Schwartz K, Komajda M. Charron P, et al. Among authors: bonne g. Eur Heart J. 1998 Jan;19(1):139-45. doi: 10.1053/euhj.1997.0575. Eur Heart J. 1998. PMID: 9503187

7

Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy.

Flavigny J, Richard P, Isnard R, Carrier L, Charron P, Bonne G, Forissier JF, Desnos M, Dubourg O, Komajda M, Schwartz K, Hainque B. Flavigny J, et al. Among authors: bonne g. J Mol Med (Berl). 1998 Mar;76(3-4):208-14. doi: 10.1007/s001090050210. J Mol Med (Berl). 1998. PMID: 9535554

8

Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene.

Charron P, Dubourg O, Desnos M, Bennaceur M, Carrier L, Camproux AC, Isnard R, Hagege A, Langlard JM, Bonne G, Richard P, Hainque B, Bouhour JB, Schwartz K, Komajda M. Charron P, et al. Among authors: bonne g. Circulation. 1998 Jun 9;97(22):2230-6. doi: 10.1161/01.cir.97.22.2230. Circulation. 1998. PMID: 9631872

9

Familial hypertrophic cardiomyopathy: from mutations to functional defects.

Bonne G, Carrier L, Richard P, Hainque B, Schwartz K. Bonne G, et al. Circ Res. 1998 Sep 21;83(6):580-93. doi: 10.1161/01.res.83.6.580. Circ Res. 1998. PMID: 9742053 Review.

10

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children.

Charron P, Dubourg O, Desnos M, Bouhour JB, Isnard R, Hagege A, Carrier L, Bonne G, Tesson F, Richard P, Hainque B, Schwartz K, Komajda M. Charron P, et al. Among authors: bonne g. Eur Heart J. 1998 Sep;19(9):1377-82. doi: 10.1053/euhj.1998.1049. Eur Heart J. 1998. PMID: 9792264 Clinical Trial.

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