Publications by authors named "Said Acharfi"

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A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tachycardia/bradycardia.
Chien-Chih Chang, Said Acharfi, Mei-Hwan Wu, Fu-Tien Chiang, Jou-Kou Wang

Cardiovasc Res· November 2004

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The C-terminal region as a modulator of rNa(v)1.7 and rNa(v)1.8 expression levels.
Kausalia Vijayaragavan, Said Acharfi, Mohamed Chahine

FEBS Lett· February 2004

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A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation.
Dagmar I Keller, Said Acharfi, Etienne Delacrétaz, Nawal Benammar, Martin Rotter

J Mol Cell Cardiol· December 2003

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Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome.
Dominic Deschênes, Said Acharfi, Valerie Pouliot, Robert Hegele, Andrew Krahn

Can J Physiol Pharmacol· February 2003

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Expression and intracellular localization of an SCN5A double mutant R1232W/T1620M implicated in Brugada syndrome.
Ghayath Baroudi, Said Acharfi, Chantal Larouche, Mohamed Chahine

Circ Res· January 2002

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