Baroudi G - Search Results

1

Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome.

Baroudi G, Napolitano C, Priori SG, Del Bufalo A, Chahine M. Baroudi G, et al. Can J Cardiol. 2004 Mar 15;20(4):425-30. Can J Cardiol. 2004. PMID: 15057319

2

Expression and intracellular localization of an SCN5A double mutant R1232W/T1620M implicated in Brugada syndrome.

Baroudi G, Acharfi S, Larouche C, Chahine M. Baroudi G, et al. Circ Res. 2002 Jan 11;90(1):E11-6. Circ Res. 2002. PMID: 11786529

3

SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells.

Baroudi G, Carbonneau E, Pouliot V, Chahine M. Baroudi G, et al. FEBS Lett. 2000 Feb 4;467(1):12-6. doi: 10.1016/s0014-5793(00)01099-1. FEBS Lett. 2000. PMID: 10664447 Free article.

4

Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes.

Baroudi G, Chahine M. Baroudi G, et al. FEBS Lett. 2000 Dec 29;487(2):224-8. doi: 10.1016/s0014-5793(00)02360-7. FEBS Lett. 2000. PMID: 11150514 Free article.

5

Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G).

Baroudi G, Pouliot V, Denjoy I, Guicheney P, Shrier A, Chahine M. Baroudi G, et al. Circ Res. 2001 Jun 22;88(12):E78-83. doi: 10.1161/hh1201.093270. Circ Res. 2001. PMID: 11420310

6

Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes.

Deschênes I, Baroudi G, Berthet M, Barde I, Chalvidan T, Denjoy I, Guicheney P, Chahine M. Deschênes I, et al. Among authors: baroudi g. Cardiovasc Res. 2000 Apr;46(1):55-65. doi: 10.1016/s0008-6363(00)00006-7. Cardiovasc Res. 2000. PMID: 10727653

7

A newly characterized SCN5A mutation underlying Brugada syndrome unmasked by hyperthermia.

Mok NS, Priori SG, Napolitano C, Chan NY, Chahine M, Baroudi G. Mok NS, et al. Among authors: baroudi g. J Cardiovasc Electrophysiol. 2003 Apr;14(4):407-11. doi: 10.1046/j.1540-8167.2003.02379.x. J Cardiovasc Electrophysiol. 2003. PMID: 12741714

8

Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block.

Lupoglazoff JM, Cheav T, Baroudi G, Berthet M, Denjoy I, Cauchemez B, Extramiana F, Chahine M, Guicheney P. Lupoglazoff JM, et al. Among authors: baroudi g. Circ Res. 2001 Jul 20;89(2):E16-21. doi: 10.1161/hh1401.095087. Circ Res. 2001. PMID: 11463728

9

Phosphorylation of the consensus sites of protein kinase A on alpha1D L-type calcium channel.

Ramadan O, Qu Y, Wadgaonkar R, Baroudi G, Karnabi E, Chahine M, Boutjdir M. Ramadan O, et al. Among authors: baroudi g. J Biol Chem. 2009 Feb 20;284(8):5042-9. doi: 10.1074/jbc.M809132200. Epub 2008 Dec 11. J Biol Chem. 2009. PMID: 19074150 Free PMC article.

10

Protein kinase C activation inhibits Cav1.3 calcium channel at NH2-terminal serine 81 phosphorylation site.

Baroudi G, Qu Y, Ramadan O, Chahine M, Boutjdir M. Baroudi G, et al. Am J Physiol Heart Circ Physiol. 2006 Oct;291(4):H1614-22. doi: 10.1152/ajpheart.00095.2006. Am J Physiol Heart Circ Physiol. 2006. PMID: 16973824 Free article.

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