Authors:
Lupoglazoff, JM
Cheav, T
Baroudi, G
Berthet, M
Denjoy, L
Cauchemez, B
Extramiana, F
Chahine, M
Guicheney, P
Citation: Jm. Lupoglazoff et al., Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block, CIRCUL RES, 89(2), 2001, pp. E16-E21
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
Authors:
Lupoglazoff, JM
Denjoy, I
Berthet, M
Hainque, B
Vaksmann, G
Klug, D
Villain, E
Lucet, V
Guicheney, P
Coumel, P
Citation: Jm. Lupoglazoff et al., T wave abnormalities on Holter monitoring of congenital long QT syndrome: Phenotype marker of a mutation in LQT2 (HERG), ARCH MAL C, 94(5), 2001, pp. 470-478
Authors:
Deschenes, I
Baroudi, G
Berthet, M
Barde, I
Chalvidan, T
Denjoy, I
Guicheney, P
Chahine, M
Citation: I. Deschenes et al., Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes, CARDIO RES, 46(1), 2000, pp. 55-65
Authors:
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
Citation: M. Berthet et al., C-terminal HERG mutations - The role of hypokalemia and a KCNQ1-associatedmutation in cardiac event occurrence, CIRCULATION, 99(11), 1999, pp. 1464-1470