Որոնման արդյունքները - Denjoy, Isabelle
- Ցուցադրվում են 1 - 20 արդյունքները 29
- Գնացեք Հաջորդ էջ
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Impact of the control of symptomatic paroxysmal atrial fibrillation on health-related quality of life Guédon-Moreau, Laurence, Capucci, Alessandro, Denjoy, Isabelle, Morgan, Caroline Claire, Périer, Antoine, Leplège, Alain, Kacet, Salem
Հրապարակվել է 2010Տեքստ -
3
Challenging indication of cardioverter defibrillator implantation after sudden cardiac arrest in the very young: a case series of catecholaminergic polymorphic ventricular tachycar... Maltret, Alice, Benaich, Fatima Azzahrae, Rendu, John, Fressart, Véronique, Roux-Buisson, Nathalie, Bonnet, Damien, Denjoy, Isabelle
Հրապարակվել է 2021Տեքստ -
4
Gene‐Specific Effect of Beta‐Adrenergic Blockade on Corrected QT Interval in the Long QT Syndrome Extramiana, Fabrice, Maison‐Blanche, Pierre, Denjoy, Isabelle, De Jode, Patrick, Messali, Anne, Labbé, Jean‐Philippe, Leenhardt, Antoine
Հրապարակվել է 2013Տեքստ -
5
Salbutamol Worsens the Autonomic Nervous System Dysfunction of Children With Sickle Cell Disease Bokov, Plamen, El Jurdi, Houmam, Denjoy, Isabelle, Peiffer, Claudine, Medjahdi, Noria, Holvoet, Laurent, Benkerrou, Malika, Delclaux, Christophe
Հրապարակվել է 2020Տեքստ -
6
Reference values of electrographic and cardiac ultrasound parameters in Russian healthy children and adolescents Landon, Geraldine, Denjoy, Isabelle, Clero, Enora, Silenok, Aleksandr, Kurnosova, Irina, Butsenin, Andrey, Gourmelon, Patrick, Jourdain, Jean-Rene
Հրապարակվել է 2021Տեքստ -
7
A SPRY1 domain cardiac ryanodine receptor variant associated with short-coupled torsade de pointes Touat-Hamici, Zahia, Blancard, Malorie, Ma, Ruifang, Lin, Lianyun, Iddir, Yasmine, Denjoy, Isabelle, Leenhardt, Antoine, Yuchi, Zhiguang, Guicheney, Pascale
Հրապարակվել է 2021Տեքստ -
8
Genotype- and Sex-Specific QT-RR Relationship in the Type-1 Long-QT Syndrome Couderc, Jean-Philippe, Xia, Xiaojuan, Denjoy, Isabelle, Extramiana, Fabrice, Maison-Blanche, Pierre, Moss, Arthur J., Zareba, Wojciech, Lopes, Coeli M.
Հրապարակվել է 2012Տեքստ -
9
Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Na(v)1.5 α-subunits Clatot, Jérôme, Ziyadeh-Isleem, Azza, Maugenre, Svetlana, Denjoy, Isabelle, Liu, Haiyan, Dilanian, Gilles, Hatem, Stéphane N., Deschênes, Isabelle, Coulombe, Alain, Guicheney, Pascale, Neyroud, Nathalie
Հրապարակվել է 2012Տեքստ -
10
A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation Ziyadeh-Isleem, Azza, Clatot, Jérôme, Duchatelet, Sabine, Gandjbakhch, Estelle, Denjoy, Isabelle, Hidden-Lucet, Françoise, Hatem, Stéphane, Deschênes, Isabelle, Coulombe, Alain, Neyroud, Nathalie, Guicheney, Pascale
Հրապարակվել է 2014Տեքստ -
11
Is exposure to ionising radiation associated with childhood cardiac arrhythmia in the Russian territories contaminated by the Chernobyl fallout? A cross-sectional population-based... Jourdain, Jean-Rene, Landon, Geraldine, Clero, Enora, Doroshchenko, Vladimir, Silenok, Aleksandr, Kurnosova, Irina, Butsenin, Andrei, Denjoy, Isabelle, Franck, Didier, Heuze, Jean-Pierre, Gourmelon, Patrick
Հրապարակվել է 2018Տեքստ -
12
Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation State 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
Հրապարակվել է 2020Տեքստ -
13
R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation 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.
Հրապարակվել է 2010Տեքստ -
14
A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic Response 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
Հրապարակվել է 2021Տեքստ -
15
High-risk Long QT Syndrome Mutations in the Kv7.1 (KCNQ1) Pore Disrupt the Molecular Basis for Rapid K(+) Permeation 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.
Հրապարակվել է 2012Տեքստ -
16
A standardised hERG phenotyping pipeline to evaluate KCNH2 genetic variant pathogenicity 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
Հրապարակվել է 2021Տեքստ -
17
Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction 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
Հրապարակվել է 2016Տեքստ -
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The genetics underlying acquired long QT syndrome: impact for genetic screening 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
Հրապարակվել է 2016Տեքստ -
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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 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
Հրապարակվել է 2021Տեքստ -
20
Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human 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
Հրապարակվել է 2012Տեքստ