Search Results - Myriam Berthet

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  1. 1
    Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population

    Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population by Laëtitia Gouas, Viviane Nicaud, Myriam Berthet, Anne Forhan, Laurence Tiret, Beverley Balkau, Pascale Guicheney

    Published 2005
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  2. 2
    Homozygous <i>SCN5A</i> Mutation in Long-QT Syndrome With Functional Two-to-One Atrioventricular Block

    Homozygous <i>SCN5A</i> Mutation in Long-QT Syndrome With Functional Two-to-One Atrioventricular Block by Jean‐Marc Lupoglazoff, T. Cheav, Ghayath Baroudi, Myriam Berthet, Isabelle Denjoy, B Cauchemez, Fabrice Extramiana, Mohamed Chahine, Pascale Guicheney

    Published 2001
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  3. 3
    Long QT syndrome in neonates

    Long QT syndrome in neonates by Jean‐Marc Lupoglazoff, Isabelle Denjoy, E Villain, Véronique Fressart, Françoise Simon, A Bozio, Myriam Berthet, N. Benammar, Bernard Hainque, Pascale Guicheney

    Published 2004
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  4. 4
    Reactivation of the Epicardium at the Origin of Myocardial Fibro-Fatty Infiltration During the Atrial Cardiomyopathy

    Reactivation of the Epicardium at the Origin of Myocardial Fibro-Fatty Infiltration During the Atrial Cardiomyopathy by Nadine Suffee, Thomas Moore‐Morris, Bernd Jagla, Nathalie Mougenot, Gilles Dilanian, Myriam Berthet, Julie Proukhnitzky, P. Le Prince, David‐Alexandre Trégouët, Michel Pucéat, Stéphane N. Hatem

    Published 2020
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  5. 5
    C-terminal <i>HERG</i> Mutations

    C-terminal <i>HERG</i> Mutations by Myriam Berthet, Isabelle Denjoy, Claire Donger, L. Demay, Hicham Hammoude, Didier Klug, Eric Schulze‐Bahr, Pascale Richard, Harald Funke, Ketty Schwartz, P Coumel, Bernard Hainque, Pascale Guicheney

    Published 1999
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  6. 6
    Notched T Waves on Holter Recordings Enhance Detection of Patients With LQT2 ( <i>HERG</i> ) Mutations

    Notched T Waves on Holter Recordings Enhance Detection of Patients With LQT2 ( <i>HERG</i> ) Mutations by Jean‐Marc Lupoglazoff, Isabelle Denjoy, Myriam Berthet, Nathalie Neyroud, L. Demay, Pascale Richard, Bernard Hainque, Guy Vaksmann, Didier Klug, Antoine Leenhardt, Gaston F. Maillard, P Coumel, Pascale Guicheney

    Published 2001
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  7. 7
    Association of Serum Cholesterol Efflux Capacity With Mortality in Patients With ST-Segment Elevation Myocardial Infarction

    Association of Serum Cholesterol Efflux Capacity With Mortality in Patients With ST-Segment Elevation Myocardial Infarction by Maryse Guérin, Johanne Silvain, Julie Gall, Maryam Darabi, Myriam Berthet, Éric Frisdal, Marie Hauguel‐Moreau, Michel Zeitouni, Mathieu Kernéis, Benoît Lattuca, Delphine Brugier, Jean‐Philippe Collet, Philippe Lesnik, Gilles Montalescot

    Published 2018
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  8. 8
    Cardiac MR Strain: A Noninvasive Biomarker of Fibrofatty Remodeling of the Left Atrial Myocardium

    Cardiac MR Strain: A Noninvasive Biomarker of Fibrofatty Remodeling of the Left Atrial Myocardium by A Huber, Jérôme Lamy, Amer Rahhal, Morgane Evin, Fabrice Atassi, Carine Defrance, Guillaume Lebreton, Karine Clément, Myriam Berthet, Richard Isnard, Pascal Leprince, Philippe Cluzel, Stéphane N. Hatem, Nadjia Kachenoura, Alban Redheuil

    Published 2017
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  9. 9
    R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation

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

    Published 2010
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  10. 10
    Female Predominance and Transmission Distortion in the Long-QT Syndrome

    Female Predominance and Transmission Distortion in the Long-QT Syndrome by Medea Imboden, Heikki Swan, Isabelle Denjoy, Irene M. van Langen, Päivi Johanna Latinen-Forsblom, Carlo Napolitano, Véronique Fressart, G Breithardt, Myriam Berthet, Silvia G. Priori, Bernard Hainque, Arthur A.M. Wilde, Eric Schulze‐Bahr, Josué Feingold, Pascale Guicheney

    Published 2006
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  11. 11
    <i>MOG1</i>

    <i>MOG1</i> by Darouna Kattygnarath, Svetlana Maugenre, Nathalie Neyroud, Elise Balse, Carole Ichaï, Isabelle Denjoy, Gilles Dilanian, Raphaël P. Martins, Véronique Fressart, Myriam Berthet, Jean‐Jacques Schott, Antoine Leenhardt, Vincent Probst, Hervé Le Marec, Bernard Hainque, Alain Coulombe, Stéphane N. Hatem, Pascale Guicheney

    Published 2011
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  12. 12
    The genetics underlying acquired long QT syndrome: impact for genetic screening

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

    Published 2015
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  13. 13
    Identification of a <i>KCNQ1</i> Polymorphism Acting as a Protective Modifier Against Arrhythmic Risk in Long-QT Syndrome

    Identification of a <i>KCNQ1</i> Polymorphism Acting as a Protective Modifier Against Arrhythmic Risk in Long-QT Syndrome by Sabine Duchatelet, Lia Crotti, Rachel A. Peat, Isabelle Denjoy, Hideki Itoh, Myriam Berthet, Seiko Ohno, Véronique Fressart, Maria Cristina Monti, Cristina Crocamo, Matteo Pedrazzini, Federica Dagradi, Alessandro Vicentini, Didier Klug, Paul A. Brink, Althea Goosen, Heikki Swan, Lauri Toivonen, Annukka M. Lahtinen, Kimmo Kontula, Wataru Shimizu, Minoru Horie, Alfred L. George, David‐Alexandre Trégouët, Pascale Guicheney, Peter J. Schwartz

    Published 2013
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  14. 14
    An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

    An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing by Jamie D. Kapplinger, David J. Tester, Mariëlle Alders, Begoña Benito, Myriam Berthet, Josép Brugada, Pedro Brugada, Véronique Fressart, Alejandra Guerchicoff, Carole Harris‐Kerr, Shiro Kamakura, Florence Kyndt, Tamara T. Koopmann, Yoshihiro Miyamoto, Ryan Pfeiffer, Guido D. Pollevick, Vincent Probst, Sven Zumhagen, Matteo Vatta, Jeffrey A. Towbin, Wataru Shimizu, Eric Schulze‐Bahr, Charles Antzelevitch, Benjamin A. Salisbury, Pascale Guicheney, Arthur A.M. Wilde, Ramón Brugada, Jean‐Jacques Schott, Michael J. Ackerman

    Published 2009
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  15. 15
    Role of common and rare variants in <i>SCN10A</i>: results from the Brugada syndrome QRS locus gene discovery collaborative study

    Role of common and rare variants in <i>SCN10A</i>: results from the Brugada syndrome QRS locus gene discovery collaborative study by Elijah R. Behr, Eleonora Savio‐Galimberti, Julien Barc, Anders G. Holst, Evmorfia Petropoulou, Bram P. Prins, Javad Jabbari, Margherita Torchio, Myriam Berthet, Yuka Mizusawa, Tao Yang, Eline A. Nannenberg, Federica Dagradi, Peter Weeke, Rachel Bastiaenan, Michael J. Ackerman, Stig Haunsø, Antoine Leenhardt, Stefan Kääb, Vincent Probst, Richard Redon, Sanjay Sharma, Arthur A.M. Wilde, Jacob Tfelt‐Hansen, Peter J. Schwartz, D M Roden, Connie R. Bezzina, Morten S. Olesen, Dawood Darbar, Pascale Guicheney, Lia Crotti, Yalda Jamshidi

    Published 2015
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