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Filtres: Author is Benammar, Nawal [Enlever les filtres]

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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