Publications | Cervo Brain Research Centre

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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, and 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, pp. 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., and 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, pp. 131-40, 2013.

2012

A. Moreau, Keller, D. I., Huang, H., Fressart, V., Schmied, C., Timour, Q., and 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., and 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, pp. 79-85, 2008.

2003

D. I. Keller, Acharfi, S., Delacrétaz, E., Benammar, N., Rotter, M., Pfammatter, J. Pierre, Fressart, V., Guicheney, P., and 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, pp. 1513-21, 2003.

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