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Results: 1-6 |
Results: 6

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

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
Risultati: 1-6 |