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The Journal of Membrane Biology|December 11, 2002
Somatic gene transfer of tagged K+ channel fragments to probe trafficking and electrical function in epithelial cells and cardiac myocytesN Neyroud, I Deschênes, M Akao, et al.
The EMBO Journal|October 6, 1997
Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmiasC Chouabe, N Neyroud, P Guicheney, et al.
Presse Medicale (Paris, France : 1983)|October 13, 1998
[Congenital long QT syndrome]J M Lupoglazoff, I Denjoy, N Neyroud, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|February 24, 2001
[Ventricular repolarization and Holter monitoring. Effect of sympathetic blockage on the QT/RR ratio]F Extramiana, R Tavernier, P Maison-Blanche, et al.
The American Journal of Cardiology|March 12, 1999
QT interval and arrhythmic risk assessment after myocardial infarctionF Extramiana, N Neyroud, H V Huikuri, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|December 1, 1995
[Dynamics of ventricular repolarisation]A Leenhardt, P Maison-Blanche, I Denjoy, et al.
American Journal of Human Genetics|March 26, 1999
Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmiasR Mohammad-Panah, S Demolombe, N Neyroud, et al.
Cardiovascular Research|March 23, 2000
Novel mutations in KvLQT1 that affect Iks activation through interactions with IskC Chouabe, N Neyroud, P Richard, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndromeN Neyroud, I Denjoy, C Donger, et al.
Circulation|December 31, 1997
KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndromeC Donger, I Denjoy, M Berthet, et al.
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