Search Results - Can Hasdemir
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1
Inhibition of Cardiac Ca <sup>2+</sup> Release Channels (RyR2) Determines Efficacy of Class I Antiarrhythmic Drugs in Catecholaminergic Polymorphic Ventricular Tachycardia by Hyun Seok Hwang, Can Hasdemir, Derek R. Laver, Divya Mehra, Kutsal Turhan, Michela Faggioni, Huiyong Yin, Björn C. Knollmann
Published 2011Artigo -
2
J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge by Charles Antzelevitch, Gan-Xin Yan, Michael J. Ackerman, Martin Borggrefe, Domenico Corrado, Jihong Guo, Ihor Gussak, Can Hasdemir, Minoru Horie, Heikki V. Huikuri, Changsheng Ma, Hiroshi Morita, Gi‐Byoung Nam, Frédéric Sacher, Wataru Shimizu, Sami Viskin, Arthur A.M. Wilde
Published 2016Revisão -
3
J‐Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge by Charles Antzelevitch, Gan‐Xin Yan, Michael J. Ackerman, Martin Borggrefe, Domenico Corrado, Jihong Guo, Ihor Gussak, Can Hasdemir, Minoru Horie, Heikki V. Huikuri, Changsheng Ma, Hiroshi Morita, Gi‐Byoung Nam, Frédéric Sacher, Wataru Shimizu, Sami Viskin, Arthur A.M. Wilde
Published 2016Artigo -
4
J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge by Charles Antzelevitch, Gan‐Xin Yan, Michael J. Ackerman, Martin Borggrefe, Domenico Corrado, Jihong Guo, Ihor Gussak, Can Hasdemir, Minoru Horie, Heikki V. Huikuri, Changsheng Ma, Hiroshi Morita, Gi‐Byoung Nam, Frédéric Sacher, Wataru Shimizu, Sami Viskin, Arthur A.M. Wilde
Published 2016Revisão -
5
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans by Hiroshi Watanabe, Tamara T. Koopmann, Solena Le Scouarnec, Tao Yang, Christiana R. Ingram, Jean‐Jacques Schott, Sophie Demolombe, Vincent Probst, Frédéric Anselme, Denis Escande, Ans C.P. Wiesfeld, Arne Pfeufer, Stefan Kääb, Hans Wichmann, Can Hasdemir, Yoshifusa Aizawa, Arthur A.M. Wilde, Dan M. Roden, Connie R. Bezzina
Published 2008Artigo -
6
A Connexin40 Mutation Associated With a Malignant Variant of Progressive Familial Heart Block Type I by Naomasa Makita, Akiko Seki, Naokata Sumitomo, Halina Chkourko, Shigetomo Fukuhara, Hiroshi Watanabe, Wataru Shimizu, Connie R. Bezzina, Can Hasdemir, Hideo Mugishima, Takeru Makiyama, Alban‐Elouen Baruteau, Estelle Baron, Minoru Horie, Nobuhisa Hagiwara, Arthur A.M. Wilde, Vincent Probst, Hervé Le Marec, Dan M. Roden, Naoki Mochizuki, Jean‐Jacques Schott, Mario Delmar
Published 2012Artigo -
7
Mutations in SCN10A Are Responsible for a Large Fraction of Cases of Brugada Syndrome by Dan Hu, Hector Barajas‐Martínez, Ryan Pfeiffer, Fabio Dezi, Jenna Pfeiffer, Thorsten Buch, Matthew J. Betzenhauser, Luiz Belardinelli, Kristopher M. Kahlig, Sridharan Rajamani, Harry DeAntonio, Robert J. Myerburg, Hiroyuki Ito, Pramod Deshmukh, Mark Marieb, Gi‐Byoung Nam, Atul Bhatia, Can Hasdemir, Michel Haı̈ssaguerre, Christian Veltmann, Rainer Schimpf, Martin Borggrefe, Sami Viskin, Charles Antzelevitch
Published 2014Artigo
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