Canlyniadau Chwilio - Denjoy, Isabelle

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation State gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation gan 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.

Cael y testun llawn Cael y testun llawn Cael y testun llawn

A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic Response gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

High-risk Long QT Syndrome Mutations in the Kv7.1 (KCNQ1) Pore Disrupt the Molecular Basis for Rapid K(+) Permeation gan 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.

Cael y testun llawn Cael y testun llawn Cael y testun llawn

A standardised hERG phenotyping pipeline to evaluate KCNH2 genetic variant pathogenicity gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

The genetics underlying acquired long QT syndrome: impact for genetic screening gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Mutation location and I  (Ks) regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn