Resultados de procura - Denjoy, Isabelle

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

Ligazón do recurso Ligazón do recurso Ligazón do recurso

Impact of the control of symptomatic paroxysmal atrial fibrillation on health-related quality of life por 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... por Maltret, Alice, Benaich, Fatima Azzahrae, Rendu, John, Fressart, Véronique, Roux-Buisson, Nathalie, Bonnet, Damien, Denjoy, Isabelle

Ligazón do recurso Ligazón do recurso Ligazón do recurso

Gene‐Specific Effect of Beta‐Adrenergic Blockade on Corrected QT Interval in the Long QT Syndrome por 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 por 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 por 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 por 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 por Couderc, Jean-Philippe, Xia, Xiaojuan, Denjoy, Isabelle, Extramiana, Fabrice, Maison-Blanche, Pierre, Moss, Arthur J., Zareba, Wojciech, Lopes, Coeli M.

Ligazón do recurso Ligazón do recurso Ligazón do recurso

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

Ligazón do recurso Ligazón do recurso Ligazón do recurso

A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation por 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... por 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 por 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 por 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 por 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 por 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 por 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

Ligazón do recurso Ligazón do recurso Ligazón do recurso

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