Coumel P - Search Results

1

Exclusion of KCNE1 (IsK) as a candidate gene for Jervell and Lange-Nielsen syndrome.

Tesson F, Donger C, Denjoy I, Berthet M, Bennaceur M, Petit C, Coumel P, Schwarts K, Guicheney P. Tesson F, et al. Among authors: coumel p. J Mol Cell Cardiol. 1996 Sep;28(9):2051-5. doi: 10.1006/jmcc.1996.0198. J Mol Cell Cardiol. 1996. PMID: 8899564

2

Readjusting the localization of long QT syndrome gene on chromosome 11p15.

Dausse E, Denjoy I, Kahlem P, Bennaceur M, Fauré S, Weissenbach J, Coumel P, Schwartz K, Guicheney P. Dausse E, et al. Among authors: coumel p. C R Acad Sci III. 1995 Aug;318(8):879-85. C R Acad Sci III. 1995. PMID: 7583778

3

A mutation in HERG associated with notched T waves in long QT syndrome.

Dausse E, Berthet M, Denjoy I, André-Fouet X, Cruaud C, Bennaceur M, Fauré S, Coumel P, Schwartz K, Guicheney P. Dausse E, et al. Among authors: coumel p. J Mol Cell Cardiol. 1996 Aug;28(8):1609-15. doi: 10.1006/jmcc.1996.0151. J Mol Cell Cardiol. 1996. PMID: 8877771

4

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: coumel p. Nat Genet. 1997 Feb;15(2):186-9. doi: 10.1038/ng0297-186. Nat Genet. 1997. PMID: 9020846

5

KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome.

Donger C, Denjoy I, Berthet M, Neyroud N, Cruaud C, Bennaceur M, Chivoret G, Schwartz K, Coumel P, Guicheney P. Donger C, et al. Among authors: coumel p. Circulation. 1997 Nov 4;96(9):2778-81. doi: 10.1161/01.cir.96.9.2778. Circulation. 1997. PMID: 9386136

6

Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome.

Neyroud N, Denjoy I, Donger C, Gary F, Villain E, Leenhardt A, Benali K, Schwartz K, Coumel P, Guicheney P. Neyroud N, et al. Among authors: coumel p. Eur J Hum Genet. 1998 Mar-Apr;6(2):129-33. doi: 10.1038/sj.ejhg.5200165. Eur J Hum Genet. 1998. PMID: 9781056

7

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.

Neyroud N, Richard P, Vignier N, Donger C, Denjoy I, Demay L, Shkolnikova M, Pesce R, Chevalier P, Hainque B, Coumel P, Schwartz K, Guicheney P. Neyroud N, et al. Among authors: coumel p. Circ Res. 1999 Feb 19;84(3):290-7. doi: 10.1161/01.res.84.3.290. Circ Res. 1999. PMID: 10024302

8

Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndrome.

Neyroud N, Maison-Blanche P, Denjoy I, Chevret S, Donger C, Dausse E, Fayn J, Badilini F, Menhabi N, Schwartz K, Guicheney P, Coumel P. Neyroud N, et al. Among authors: coumel p. Eur Heart J. 1998 Jan;19(1):158-65. doi: 10.1053/euhj.1997.0730. Eur Heart J. 1998. PMID: 9503190

9

C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.

Berthet M, Denjoy I, Donger C, Demay L, Hammoude H, Klug D, Schulze-Bahr E, Richard P, Funke H, Schwartz K, Coumel P, Hainque B, Guicheney P. Berthet M, et al. Among authors: coumel p. Circulation. 1999 Mar 23;99(11):1464-70. doi: 10.1161/01.cir.99.11.1464. Circulation. 1999. PMID: 10086971

10

[Congenital long QT syndrome. The value of genetics in prognostic evaluation].

Denjoy I, Lupoglazoff JM, Donger C, Berthet M, Richard P, Neyroud N, Villain E, Lucet V, Coumel P, Guicheney P. Denjoy I, et al. Among authors: coumel p. Arch Mal Coeur Vaiss. 1999 May;92(5):557-63. Arch Mal Coeur Vaiss. 1999. PMID: 10367071 French.

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