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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.

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.

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