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Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia de réir Gaetano Maria De Ferrari, Veronica Dusi, Carla Spazzolini, J. Martijn Bos, Dominic J. Abrams, Charles I. Berul, Lia Crotti, Andrew M. Davis, Michael Eldar, М. С. Харлап, Asaad Khoury, Andrew D. Krahn, Antoine Leenhardt, Christopher R. Moir, Attilio Odero, Louise R.A. Olde Nordkamp, Thomas Paul, Ferran Rosés‐Noguer, M. А. Shkolnikova, Jan Till, Arthur A.M. Wilde, Michael J. Ackerman, Peter J. Schwartz

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The use of implantable cardioverter defibrillators in pediatric patients de réir Valquíria Pelisser Campagnucci, A Silva, Wilson Lopes Pereira, Alexey Pomares Peroni, Eduardo Gregório Chamlian, Sylvio M. A. Gandra, A Scatolini, Uelra Rita Lourenço, FAC Silva, Luiz Antônio Rivetti

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Catecholaminergic Polymorphic Ventricular Tachycardia de réir Krystien V.V. Lieve, Christian van der Werf, Arthur A.M. Wilde

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Nadolol decreases the incidence and severity of ventricular arrhythmias during exercise stress testing compared with β1-selective β-blockers in patients with catecholaminergic poly... de réir Ida S. Leren, Jørg Saberniak, Eman Majid, Trine F. Håland, Thor Edvardsen, Kristina H. Haugaa

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Antiarrhythmic Effects of Dantrolene in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Replication of the Responses Using iPSC Models de réir Kirsi Penttinen, Heikki Swan, Sari Vanninen, Jere Paavola, Annukka M. Lahtinen, Kimmo Kontula, Katriina Aalto‐Setälä

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Inherited arrhythmias: The cardiac channelopathies de réir ShashankP Behere, StevenN Weindling

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Functional abnormalities in iPSC‐derived cardiomyocytes generated from CPVT1 and CPVT2 patients carrying ryanodine or calsequestrin mutations de réir Atara Novak, Lili Barad, Avraham Lorber, Mihaela Gherghiceanu, Irina Reiter, Binyamin Eisen, Liron Eldor, Joseph Itskovitz‐Eldor, Michael Eldar, Michael Arad, Ofer Binah

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Incidence and Risk Factors of Arrhythmic Events in Catecholaminergic Polymorphic Ventricular Tachycardia de réir Meiso Hayashi, Isabelle Denjoy, Fabrice Extramiana, Alice Maltret, Nathalie Roux Buisson, Jean‐Marc Lupoglazoff, Didier Klug, Miyuki Hayashi, Seiji Takatsuki, E Villain, J Kamblock, A. Messali, Pascale Guicheney, Joël Lunardi, Antoine Leenhardt

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Dantrolene, a Therapeutic Agent for Malignant Hyperthermia, Markedly Improves the Function of Failing Cardiomyocytes by Stabilizing Interdomain Interactions Within the Ryanodine Re... de réir Shigeki Kobayashi, Masafumi Yano, Takeshi Suetomi, Makoto Ono, Hiroki Tateishi, Mamoru Mochizuki, Xiaojuan Xu, Hitoshi Uchinoumi, Shinichi Okuda, Takeshi Yamamoto, Noritaka Koseki, Hiroyuki Kyushiki, Noriaki Ikemoto, Masunori Matsuzaki

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Calmodulin kinase II–mediated sarcoplasmic reticulum Ca2+ leak promotes atrial fibrillation in mice de réir Mihail G. Chelu, Satyam Sarma, Subeena Sood, Sufen Wang, Ralph J. van Oort, Darlene G. Skapura, Na Li, Marco Santonastasi, Frank U. Müller, Wilhelm Schmitz, Ulrich Schotten, Mark E. Anderson, Miguel Valderrábano, Dobromir Dobrev, Xander H.T. Wehrens

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Sudden Death in Familial Polymorphic Ventricular Tachycardia Associated With Calcium Release Channel (Ryanodine Receptor) Leak de réir Stephan E. Lehnart, Xander H.T. Wehrens, Päivi J. Laitinen, Steven Reiken, Shi-Xiang Deng, Zhenzhuang Cheng, Donald W. Landry, Kimmo Kontula, Heikki Swan, Andrew R. Marks

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Cell Model of Catecholaminergic Polymorphic Ventricular Tachycardia Reveals Early and Delayed Afterdepolarizations de réir Kirsi Kujala, Jere Paavola, Anna Lahti, Kim Larsson, Mari Pekkanen-Mattila, Matti Viitasalo, Annukka M. Lahtinen, Lauri Toivonen, Kimmo Kontula, Heikki Swan, Mika Laine, Olli Silvennoinen, Katriina Aalto‐Setälä

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Genetic Testing for Potentially Lethal, Highly Treatable Inherited Cardiomyopathies/Channelopathies in Clinical Practice de réir David J. Tester, Michael J. Ackerman

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Mice with the R176Q cardiac ryanodine receptor mutation exhibit catecholamine-induced ventricular tachycardia and cardiomyopathy de réir Prince J. Kannankeril, Brett M. Mitchell, Sanjeewa A. Goonasekera, Mihail G. Chelu, Wei Zhang, Subeena Sood, Debra L. Kearney, Cristina I. Danila, Mariella De Biasi, Xander H.T. Wehrens, Robia G. Pautler, Dan M. Roden, George E. Taffet, Robert T. Dirksen, Mark E. Anderson, Susan L. Hamilton

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RyR2 mutations linked to ventricular tachycardia and sudden death reduce the threshold for store-overload-induced Ca ²⁺ release (SOICR) de réir Dawei Jiang, Bailong Xiao, Dongmei Yang, Ruiwu Wang, Philip Choi, Lin Zhang, Heping Cheng, S. R. Wayne Chen

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Successful Catheter Ablation of Bidirectional Ventricular Premature Contractions Triggering Ventricular Fibrillation in Catecholaminergic Polymorphic Ventricular Tachycardia With <... de réir Takashi Kaneshiro, Yoshihisa Naruse, Akihiko Nogami, Hiroshi Tada, Kentaro Yoshida, Yukio Sekiguchi, Nobuyuki Murakoshi, Yoshiaki Kato, Hitoshi Horigome, Mihoko Kawamura, Minoru Horie, Kazutaka Aonuma

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A mechanism for sudden infant death syndrome (SIDS): Stress-induced leak via ryanodine receptors de réir David J. Tester, Miroslav Důra, Elisa Carturan, Steven Reiken, Anetta Wronska, Andrew R. Marks, Michael J. Ackerman

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Autosomal Recessive Catecholamine- or Exercise-Induced Polymorphic Ventricular Tachycardia de réir Hadas Lahat, Michael Eldar, Etgar Levy‐Nissenbaum, Tangiz Bahan, Eitan Friedman, Asad Khoury, Avraham Lorber, Daniel L. Kastner, Boleslaw Goldman, Elon Pras

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Ryanodine receptor channelopathies de réir Matthew J. Betzenhauser, Andrew R. Marks

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Drug-Induced Torsade de Pointes. From Molecular Biology to Bedside. de réir Juan Tamargo

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