Publications
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Filtres: Author is Baroudi, G [Enlever les filtres]
, « Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block. », Circ Res, vol. 89, nᵒ 2, p. E16-21, 2001.
, « Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G). », Circ Res, vol. 88, nᵒ 12, p. E78-83, 2001.
, « Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes. », FEBS Lett, vol. 487, nᵒ 2, p. 224-8, 2000.
, « Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes. », Cardiovasc Res, vol. 46, nᵒ 1, p. 55-65, 2000.
, « SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells. », FEBS Lett, vol. 467, nᵒ 1, p. 12-6, 2000.
