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Results: 1-8 |
Results: 8
Notched T waves on Holter recordings enhance detection of patients with LQT2 (HERG) mutations
Authors: Lupoglazoff, JM Denjoy, I Berthet, M Neyroud, N Demay, L Richard, P Hainque, B Vaksmann, G Klug, D Leenhardt, A Maillard, G Coumel, P Guicheney, P
Citation: Jm. Lupoglazoff et al., Notched T waves on Holter recordings enhance detection of patients with LQT2 (HERG) mutations, CIRCULATION, 103(8), 2001, pp. 1095-1101
Novel mutations in KvLQT1 that affect I-ks activation through interactionswith Isk
Authors: Chouabe, C Neyroud, N Richard, P Denjoy, I Hainque, B Romey, G Drici, MD Guicheney, P Barhanin, J
Citation: C. Chouabe et al., Novel mutations in KvLQT1 that affect I-ks activation through interactionswith Isk, CARDIO RES, 45(4), 2000, pp. 971-980
Ventricular repolarisation and holter monitoring: Role of sympathetic blockade on the physiology of the QT/RR ratio
Authors: Extramiana, F Tavernier, R Maison-Blanche, P Neyroud, N Jordaens, L Leenhardt, A Coumel, P
Citation: F. Extramiana et al., Ventricular repolarisation and holter monitoring: Role of sympathetic blockade on the physiology of the QT/RR ratio, ARCH MAL C, 93(11), 2000, pp. 1277-1283
Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome
Authors: 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
Citation: N. Neyroud et al., Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome, CIRCUL RES, 84(3), 1999, pp. 290-297
Splicing mutations in KCNQ1 - A mutation hot spot at codon 344 that produces in frame transcripts
Authors: Murray, A Donger, C Fenske, C Spillman, I Richard, P Dong, YB Neyroud, N Chevalier, P Denjoy, I Carter, N Syrris, P Afzal, AR Patton, MA Guicheney, P Jeffery, S
Citation: A. Murray et al., Splicing mutations in KCNQ1 - A mutation hot spot at codon 344 that produces in frame transcripts, CIRCULATION, 100(10), 1999, pp. 1077-1084
Congenital long QT syndrome: The value of genetics in assessing the prognosis
Authors: Denjoy, I Lupoglazoff, JM Donger, C Berthet, M Richard, P Neyroud, N Villain, E Lucet, V Coumel, P Guicheney, P
Citation: I. Denjoy et al., Congenital long QT syndrome: The value of genetics in assessing the prognosis, ARCH MAL C, 92(5), 1999, pp. 557-563
Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias
Authors: Mohammad-Panah, R Demolombe, S Neyroud, N Guicheney, P Kyndt, F van den Hoff, M Baro, I Escande, D
Citation: R. Mohammad-panah et al., Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias, AM J HU GEN, 64(4), 1999, pp. 1015-1023
QT interval and arrhythmic risk assessment after myocardial infarction
Authors: Extramiana, F Neyroud, N Huikuri, HV Koistinen, MJ Coumel, P Maison-Blanche, P
Citation: F. Extramiana et al., QT interval and arrhythmic risk assessment after myocardial infarction, AM J CARD, 83(2), 1999, pp. 266
Risultati: 1-8 |