AAAAAA

   
Results: 1-5 |
Results: 5

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: Baroudi, G Pouliot, V Denjoy, I Guicheney, P Shrier, A Chahine, M
Citation: G. Baroudi et al., Novel mechanism forBrugada syndrome - Defective surface localization of anSCN5A mutant (R1432G), CIRCUL RES, 88(12), 2001, pp. E78-E83

Authors: Baroudi, G Chahine, M
Citation: G. Baroudi et M. Chahine, Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes, FEBS LETTER, 487(2), 2000, pp. 224-228

Authors: Baroudi, G Carbonneau, E Pouliot, V Chahine, M
Citation: G. Baroudi et al., SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells, FEBS LETTER, 467(1), 2000, pp. 12-16

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
Risultati: 1-5 |