Publications | Centre de recherche CERVO

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Filtres: Author is Fressart, Véronique [Enlever les filtres]

2021

Q. Plumereau, Thériault, O., Pouliot, V., Moreau, A., Morel, E., Fressart, V., Denjoy, I., Delinière, A., Bessière, F., Chevalier, P., El-Din, T. M. Gamal, et Chahine, M., « Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation State. », CJC Open, vol. 3, nᵒ 3, p. 256-266, 2021.

2013

P. Maury, Moreau, A., Hidden-Lucet, F., Leenhardt, A., Fressart, V., Berthet, M., Denjoy, I., Bennamar, N., Rollin, A., Cardin, C., Guicheney, P., et Chahine, M., « Novel SCN5A mutations in two families with "Brugada-like" ST elevation in the inferior leads and conduction disturbances. », J Interv Card Electrophysiol, vol. 37, nᵒ 2, p. 131-40, 2013.

2012

A. Moreau, Keller, D. I., Huang, H., Fressart, V., Schmied, C., Timour, Q., et Chahine, M., « Mexiletine differentially restores the trafficking defects caused by two brugada syndrome mutations. », Front Pharmacol, vol. 3, p. 62, 2012.

2008

I. Six, Hermida, J. - S., Huang, H., Gouas, L., Fressart, V., Benammar, N., Hainque, B., Denjoy, I., Chahine, M., et Guicheney, P., « The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases. », Europace, vol. 10, nᵒ 1, p. 79-85, 2008.

2003

D. I. Keller, Acharfi, S., Delacrétaz, E., Benammar, N., Rotter, M., Pfammatter, J. Pierre, Fressart, V., Guicheney, P., et Chahine, M., « A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation. », J Mol Cell Cardiol, vol. 35, nᵒ 12, p. 1513-21, 2003.

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