检索结果 - Denjoy, Isabelle

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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