Resultats de la cerca - Denjoy, Isabelle

Effect of halofantrine on QT interval in children per Siriez, Jean-Yves, Lupoglazoff, Jean-Marc, Bouchy-Bagros, Marie-Laure, Pull, Lauren, Denjoy, Isabelle

Obtenir text complet Obtenir text complet Obtenir text complet

Impact of the control of symptomatic paroxysmal atrial fibrillation on health-related quality of life per Guédon-Moreau, Laurence, Capucci, Alessandro, Denjoy, Isabelle, Morgan, Caroline Claire, Périer, Antoine, Leplège, Alain, Kacet, Salem

Obtenir text complet Obtenir text complet Obtenir text complet

Challenging indication of cardioverter defibrillator implantation after sudden cardiac arrest in the very young: a case series of catecholaminergic polymorphic ventricular tachycar... per Maltret, Alice, Benaich, Fatima Azzahrae, Rendu, John, Fressart, Véronique, Roux-Buisson, Nathalie, Bonnet, Damien, Denjoy, Isabelle

Obtenir text complet Obtenir text complet Obtenir text complet

Gene‐Specific Effect of Beta‐Adrenergic Blockade on Corrected QT Interval in the Long QT Syndrome per Extramiana, Fabrice, Maison‐Blanche, Pierre, Denjoy, Isabelle, De Jode, Patrick, Messali, Anne, Labbé, Jean‐Philippe, Leenhardt, Antoine

Obtenir text complet Obtenir text complet Obtenir text complet

Salbutamol Worsens the Autonomic Nervous System Dysfunction of Children With Sickle Cell Disease per Bokov, Plamen, El Jurdi, Houmam, Denjoy, Isabelle, Peiffer, Claudine, Medjahdi, Noria, Holvoet, Laurent, Benkerrou, Malika, Delclaux, Christophe

Obtenir text complet Obtenir text complet Obtenir text complet

Reference values of electrographic and cardiac ultrasound parameters in Russian healthy children and adolescents per Landon, Geraldine, Denjoy, Isabelle, Clero, Enora, Silenok, Aleksandr, Kurnosova, Irina, Butsenin, Andrey, Gourmelon, Patrick, Jourdain, Jean-Rene

Obtenir text complet Obtenir text complet Obtenir text complet

A SPRY1 domain cardiac ryanodine receptor variant associated with short-coupled torsade de pointes per Touat-Hamici, Zahia, Blancard, Malorie, Ma, Ruifang, Lin, Lianyun, Iddir, Yasmine, Denjoy, Isabelle, Leenhardt, Antoine, Yuchi, Zhiguang, Guicheney, Pascale

Obtenir text complet Obtenir text complet Obtenir text complet

Genotype- and Sex-Specific QT-RR Relationship in the Type-1 Long-QT Syndrome per Couderc, Jean-Philippe, Xia, Xiaojuan, Denjoy, Isabelle, Extramiana, Fabrice, Maison-Blanche, Pierre, Moss, Arthur J., Zareba, Wojciech, Lopes, Coeli M.

Obtenir text complet Obtenir text complet Obtenir text complet

Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Na(v)1.5 α-subunits per Clatot, Jérôme, Ziyadeh-Isleem, Azza, Maugenre, Svetlana, Denjoy, Isabelle, Liu, Haiyan, Dilanian, Gilles, Hatem, Stéphane N., Deschênes, Isabelle, Coulombe, Alain, Guicheney, Pascale, Neyroud, Nathalie

Obtenir text complet Obtenir text complet Obtenir text complet

A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation per Ziyadeh-Isleem, Azza, Clatot, Jérôme, Duchatelet, Sabine, Gandjbakhch, Estelle, Denjoy, Isabelle, Hidden-Lucet, Françoise, Hatem, Stéphane, Deschênes, Isabelle, Coulombe, Alain, Neyroud, Nathalie, Guicheney, Pascale

Obtenir text complet Obtenir text complet Obtenir text complet

Is exposure to ionising radiation associated with childhood cardiac arrhythmia in the Russian territories contaminated by the Chernobyl fallout? A cross-sectional population-based... per Jourdain, Jean-Rene, Landon, Geraldine, Clero, Enora, Doroshchenko, Vladimir, Silenok, Aleksandr, Kurnosova, Irina, Butsenin, Andrei, Denjoy, Isabelle, Franck, Didier, Heuze, Jean-Pierre, Gourmelon, Patrick

Obtenir text complet Obtenir text complet Obtenir text complet

Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation State per Plumereau, Quentin, Theriault, Olivier, Pouliot, Valérie, Moreau, Adrien, Morel, Elodie, Fressart, Véronique, Denjoy, Isabelle, Delinière, Antoine, Bessière, Francis, Chevalier, Philippe, Gamal El-Din, Tamer M., Chahine, Mohamed

Obtenir text complet Obtenir text complet Obtenir text complet

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation per Bartos, Daniel C., Duchatelet, Sabine, Burgess, Don E., Klug, Didier, Denjoy, Isabelle, Peat, Rachel, Lupoglazoff, Jean-Marc, Fressart, Véronique, Berthet, Myriam, Ackerman, Michael J., January, Craig T., Guicheney, Pascale, Delisle, Brian P.

Obtenir text complet Obtenir text complet Obtenir text complet

A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic Response per Blancard, Malorie, Touat-Hamici, Zahia, Aguilar-Sanchez, Yuriana, Yin, Liheng, Vaksmann, Guy, Roux-Buisson, Nathalie, Fressart, Véronique, Denjoy, Isabelle, Klug, Didier, Neyroud, Nathalie, Ramos-Franco, Josefina, Gomez, Ana Maria, Guicheney, Pascale

Obtenir text complet Obtenir text complet Obtenir text complet

High-risk Long QT Syndrome Mutations in the Kv7.1 (KCNQ1) Pore Disrupt the Molecular Basis for Rapid K(+) Permeation per Burgess, Don E., Bartos, Daniel C., Reloj, Allison R., Campbell, Kenneth S., Johnson, Jonathan N., Tester, David J., Ackerman, Michael J., Fressart, Véronique, Denjoy, Isabelle, Guicheney, Pascale, Moss, Arthur J., Ohno, Seiko, Horie, Minoru, Delisle, Brian P.

Obtenir text complet Obtenir text complet Obtenir text complet

A standardised hERG phenotyping pipeline to evaluate KCNH2 genetic variant pathogenicity per Oliveira‐Mendes, Barbara, Feliciangeli, Sylvain, Ménard, Mélissa, Chatelain, Frank, Alameh, Malak, Montnach, Jérôme, Nicolas, Sébastien, Ollivier, Béatrice, Barc, Julien, Baró, Isabelle, Schott, Jean‐Jacques, Probst, Vincent, Kyndt, Florence, Denjoy, Isabelle, Lesage, Florian, Loussouarn, Gildas, De Waard, Michel

Obtenir text complet Obtenir text complet Obtenir text complet

Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction per Itoh, Hideki, Berthet, Myriam, Fressart, Véronique, Denjoy, Isabelle, Maugenre, Svetlana, Klug, Didier, Mizusawa, Yuka, Makiyama, Takeru, Hofman, Nynke, Stallmeyer, Birgit, Zumhagen, Sven, Shimizu, Wataru, Wilde, Arthur A M, Schulze-Bahr, Eric, Horie, Minoru, Tezenas du Montcel, Sophie, Guicheney, Pascale

Obtenir text complet Obtenir text complet Obtenir text complet

The genetics underlying acquired long QT syndrome: impact for genetic screening per Itoh, Hideki, Crotti, Lia, Aiba, Takeshi, Spazzolini, Carla, Denjoy, Isabelle, Fressart, Véronique, Hayashi, Kenshi, Nakajima, Tadashi, Ohno, Seiko, Makiyama, Takeru, Wu, Jie, Hasegawa, Kanae, Mastantuono, Elisa, Dagradi, Federica, Pedrazzini, Matteo, Yamagishi, Masakazu, Berthet, Myriam, Murakami, Yoshitaka, Shimizu, Wataru, Guicheney, Pascale, Schwartz, Peter J., Horie, Minoru

Obtenir text complet Obtenir text complet Obtenir text complet

Mutation location and I  (Ks) regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region per Schwartz, Peter J, Moreno, Cristina, Kotta, Maria-Christina, Pedrazzini, Matteo, Crotti, Lia, Dagradi, Federica, Castelletti, Silvia, Haugaa, Kristina H, Denjoy, Isabelle, Shkolnikova, Maria A, Brink, Paul A, Heradien, Marshall J, Seyen, Sandrine R M, Spätjens, Roel L H M G, Spazzolini, Carla, Volders, Paul G A

Obtenir text complet Obtenir text complet Obtenir text complet

Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human per Roux-Buisson, Nathalie, Cacheux, Marine, Fourest-Lieuvin, Anne, Fauconnier, Jeremy, Brocard, Julie, Denjoy, Isabelle, Durand, Philippe, Guicheney, Pascale, Kyndt, Florence, Leenhardt, Antoine, Le Marec, Hervé, Lucet, Vincent, Mabo, Philippe, Probst, Vincent, Monnier, Nicole, Ray, Pierre F., Santoni, Elodie, Trémeaux, Pauline, Lacampagne, Alain, Fauré, Julien, Lunardi, Joël, Marty, Isabelle

Obtenir text complet Obtenir text complet Obtenir text complet