Publications | Cervo Brain Research Centre

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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.

2005

D. I. Keller, Barrane, F. - Z., Gouas, L., Martin, J., Pilote, S., Suarez, V., Osswald, S., Brink, M., Guicheney, P., Schwick, N., and Chahine, M., “A novel nonsense mutation in the SCN5A gene leads to Brugada syndrome and a silent gene mutation carrier state.”, Can J Cardiol, vol. 21, no. 11, pp. 925-31, 2005.

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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