Tesson F - Search Results

1

Systematic and quantitative view of the antiviral arsenal of prokaryotes.

Tesson F, Hervé A, Mordret E, Touchon M, d'Humières C, Cury J, Bernheim A. Tesson F, et al. Nat Commun. 2022 May 10;13(1):2561. doi: 10.1038/s41467-022-30269-9. Nat Commun. 2022. PMID: 35538097 Free PMC article.

2

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy.

Helbling-Leclerc A, Zhang X, Topaloglu H, Cruaud C, Tesson F, Weissenbach J, Tomé FM, Schwartz K, Fardeau M, Tryggvason K, et al. Helbling-Leclerc A, et al. Among authors: tesson f. Nat Genet. 1995 Oct;11(2):216-8. doi: 10.1038/ng1095-216. Nat Genet. 1995. PMID: 7550355

3

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome.

Neyroud N, Tesson F, Denjoy I, Leibovici M, Donger C, Barhanin J, Fauré S, Gary F, Coumel P, Petit C, Schwartz K, Guicheney P. Neyroud N, et al. Among authors: tesson f. Nat Genet. 1997 Feb;15(2):186-9. doi: 10.1038/ng0297-186. Nat Genet. 1997. PMID: 9020846

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. 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

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: tesson f. Genet Couns. 1997;8(2):107-14. Genet Couns. 1997. PMID: 9219008

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

7

The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation.

Tesson F, Dufour C, Moolman JC, Carrier L, al-Mahdawi S, Chojnowska L, Dubourg O, Soubrier E, Brink P, Komajda M, Guicheney P, Schwartz K, Feingold J. Tesson F, et al. J Mol Cell Cardiol. 1997 Feb;29(2):831-8. doi: 10.1006/jmcc.1996.0332. J Mol Cell Cardiol. 1997. PMID: 9140839

8

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: tesson f. Eur Heart J. 1998 Sep;19(9):1377-82. doi: 10.1053/euhj.1998.1049. Eur Heart J. 1998. PMID: 9792264 Clinical Trial.

9

Familial dilated cardiomyopathy: clinical features in French families.

Mangin L, Charron P, Tesson F, Mallet A, Dubourg O, Desnos M, Benaïsche A, Gayet C, Gibelin P, Davy JM, Bonnet J, Sidi D, Schwartz K, Komajda M. Mangin L, et al. Among authors: tesson f. Eur J Heart Fail. 1999 Dec;1(4):353-61. doi: 10.1016/s1388-9842(99)00047-1. Eur J Heart Fail. 1999. PMID: 10937948 Free article.

10

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

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