檢索結果 - Arthur AM Wilde

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  1. 1
    Genetic and Clinical Advances in Congenital Long QT Syndrome

    Genetic and Clinical Advances in Congenital Long QT Syndrome 由 Yuka Mizusawa, Minoru Horie, Arthur AM Wilde

    出版 2014
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    Revisão
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  2. 2
    How do hypertrophic cardiomyopathy mutations affect myocardial function in carriers with normal wall thickness? Assessment with cardiovascular magnetic resonance

    How do hypertrophic cardiomyopathy mutations affect myocardial function in carriers with normal wall thickness? Assessment with cardiovascular magnetic resonance 由 Tjeerd Germans, Iris K. Rüssel, Marco Götte, Marieke D. Spreeuwenberg, Pieter A. Doevendans, Yigal M. Pinto, Rob J. van der Geest, Jolanda van der Velden, Arthur AM Wilde, Albert C. van Rossum

    出版 2010
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    Artigo
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    <i><scp>TECRL</scp></i>, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both <scp>LQTS</scp> and <scp>CPVT</scp>

    <i><scp>TECRL</scp></i>, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both <scp>LQTS</scp> and <scp>CPVT</scp> 由 Harsha D. Devalla, Roselle Gélinas, Elhadi H. Aburawi, Abdelaziz Beqqali, Philippe Goyette, Christian Freund, Marie Chaix, Rafik Tadros, Hui Jiang, Antony Le Béchec, Jantine Monshouwer‐Kloots, Tom Zwetsloot, Georgios Kosmidis, Frédéric Latour, Azadeh Alikashani, Maaike Hoekstra, Jürg Schlaepfer, Christine L. Mummery, Brian J. Stevenson, Zoltán Kutalik, Antoine AF de Vries, Léna Rivard, Arthur AM Wilde, Mario Talajic, Arie O. Verkerk, Lihadh Al‐Gazali, John D. Rioux, Zahurul A. Bhuiyan, Robert Passier

    出版 2016
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    Artigo
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