Carrier L - 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: carrier l. 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

Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French families.

Schwartz K, Beckmann J, Dufour C, Faure L, Fougerousse F, Carrier L, Hengstenberg C, Cohen D, Vosberg HP, Sacrez A, et al. Schwartz K, et al. Among authors: carrier l. Circ Res. 1992 Jul;71(1):3-8. doi: 10.1161/01.res.71.1.3. Circ Res. 1992. PMID: 1606666

3

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. Among authors: carrier l. 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.

4

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. Among authors: carrier l. Nat Genet. 1995 Dec;11(4):438-40. doi: 10.1038/ng1295-438. Nat Genet. 1995. PMID: 7493026

5

Clinical and genetical heterogeneity of familial hypertrophic cardiomyopathy.

Hengstenberg C, Carrier L, Schwartz K, Maisch B. Hengstenberg C, et al. Among authors: carrier l. Herz. 1994 Apr;19(2):84-90. Herz. 1994. PMID: 8194836 Review.

6

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11.

Carrier L, Hengstenberg C, Beckmann JS, Guicheney P, Dufour C, Bercovici J, Dausse E, Berebbi-Bertrand I, Wisnewsky C, Pulvenis D, et al. Carrier L, et al. Nat Genet. 1993 Jul;4(3):311-3. doi: 10.1038/ng0793-311. Nat Genet. 1993. PMID: 8358441

7

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: carrier l. Genet Couns. 1997;8(2):107-14. Genet Couns. 1997. PMID: 9219008

8

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

9

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: carrier l. Eur Heart J. 1998 Jan;19(1):139-45. doi: 10.1053/euhj.1997.0575. Eur Heart J. 1998. PMID: 9503187

10

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: carrier l. J Mol Med (Berl). 1998 Mar;76(3-4):208-14. doi: 10.1007/s001090050210. J Mol Med (Berl). 1998. PMID: 9535554

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