Brugada syndrome and fever : Genetic and molecular characterization of patients carrying SCN5A mutations von KELLER, Dagmar I, ROUGIER, Jean-Sébastien, KUCERA, Jan P, BENAMMAR, Nawal, FRESSART, Véronique, GUICHENEY, Pascale, MADLE, Alois, FROMER, Martin, SCHLÄPFER, Jürg, ABRIEL, Hugues

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Long QT syndrome in neonates: Conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations von LUPOGLAZOFF, Jean-Marc, DENJOY, Isabelle, VILLAIN, Elisabeth, FRESSART, Véronique, SIMON, Francoise, BOZIO, André, BERTHET, Myriam, BENAMMAR, Nawal, HAINQUE, Bernard, GUICHENEY, Pascale

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A novel mutation in SCN5A, delQKP 1507–1509, causing long QT syndrome: : Role of Q1507 residue in sodium channel inactivation von Keller, Dagmar I., Acharfi, Said, Delacrétaz, Etienne, Benammar, Nawal, Rotter, Martin, Pfammatter, Jean-Pierre, Fressart, Véronique, Guicheney, Pascale, Chahine, Mohamed

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Spinocerebellar ataxia with mental retardation (SCA13) von Stevanin, Giovanni, Durr, Alexandra, Benammar, Nawal, Brice, Alexis

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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 disea... von Six, Isabelle, Hermida, Jean-Sylvain, Huang, Hai, Gouas, Laetitia, Fressart, Véronique, Benammar, Nawal, Hainque, Bernard, Denjoy, Isabelle, Chahine, Mohamed, Guicheney, Pascale

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Long QT syndrome in neonates von Lupoglazoff, Jean-Marc, Denjoy, Isabelle, Villain, Elisabeth, Fressart, Véronique, Simon, Françoise, Bozio, André, Berthet, Myriam, Benammar, Nawal, Hainque, Bernard, Guicheney, Pascale

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