Neyroud N - Search Results

1

QT interval and arrhythmic risk assessment after myocardial infarction.

Extramiana F, Neyroud N, Huikuri HV, Koistinen MJ, Coumel P, Maison-Blanche P. Extramiana F, et al. Among authors: neyroud n. Am J Cardiol. 1999 Jan 15;83(2):266-9, A6. doi: 10.1016/s0002-9149(98)00835-2. Am J Cardiol. 1999. PMID: 10073834 Clinical Trial.

2

Different circadian behavior of the apex and the end of the T wave.

Coumel P, Maison-Blanche P, Catuli D, Neyroud N, Fayn J, Rubel P. Coumel P, et al. Among authors: neyroud n. J Electrocardiol. 1995;28 Suppl:138-42. doi: 10.1016/s0022-0736(95)80039-5. J Electrocardiol. 1995. PMID: 8656101 No abstract available.

3

[Dynamics of ventricular repolarisation].

Leenhardt A, Maison-Blanche P, Denjoy I, Neyroud N, Pellerin D, Catuli D, Thomas O, Coumel P. Leenhardt A, et al. Among authors: neyroud n. Arch Mal Coeur Vaiss. 1995 Dec;88 Spec No 5:27-33. Arch Mal Coeur Vaiss. 1995. PMID: 8729297 French.

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. 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: neyroud n. Circulation. 1997 Nov 4;96(9):2778-81. doi: 10.1161/01.cir.96.9.2778. Circulation. 1997. PMID: 9386136

6

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. Eur Heart J. 1998 Jan;19(1):158-65. doi: 10.1053/euhj.1997.0730. Eur Heart J. 1998. PMID: 9503190

7

[Congenital long QT syndrome].

Lupoglazoff JM, Denjoy I, Neyroud N, Guicheney P, Casasoprana A, Coumel P. Lupoglazoff JM, et al. Among authors: neyroud n. Presse Med. 1998 Jun 13;27(21):1029-34. Presse Med. 1998. PMID: 9767826 Review. French.

8

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. Eur J Hum Genet. 1998 Mar-Apr;6(2):129-33. doi: 10.1038/sj.ejhg.5200165. Eur J Hum Genet. 1998. PMID: 9781056

9

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. Circ Res. 1999 Feb 19;84(3):290-7. doi: 10.1161/01.res.84.3.290. Circ Res. 1999. PMID: 10024302

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: neyroud n. Arch Mal Coeur Vaiss. 1999 May;92(5):557-63. Arch Mal Coeur Vaiss. 1999. PMID: 10367071 French.

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