Impact of Genetics on the Clinical Management of Channelopathies von Schwartz, Peter J., MD, Ackerman, Michael J., MD, PhD, George, Alfred L., MD, Wilde, Arthur A.M., MD, PhD

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Inherited cardiac arrhythmias von Schwartz, Peter J., Ackerman, Michael J., Antzelevitch, Charles, Bezzina, Connie R., Borggrefe, Martin, Cuneo, Bettina F., Wilde, Arthur A. M.

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Brugada Syndrome von Mizusawa, Yuka, Wilde, Arthur A.M

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Diagnosis, management and therapeutic strategies for congenital long QT syndrome von Wilde, Arthur A M, Amin, Ahmad S, Postema, Pieter G

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Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives von Semsarian, Christopher, Ingles, Jodie, Wilde, Arthur A M

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Epidemiology of inherited arrhythmias von Offerhaus, Joost A., Bezzina, Connie R., Wilde, Arthur A. M.

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Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Sodium Channel von Wilde, Arthur A.M, Brugada, Ramon

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Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers: A European Cohort Study von VAN RIJSINGEN, Ingrid A. W, ARBUSTINI, Eloisa, JENKINS, Sharon, ROWLAND, Camilla, ASLAM, Uzma, WILDE, Arthur A. M, PERROT, Andreas, PANKUWEIT, Sabine, ZWINDERMAN, Aeilko H, CHARRON, Philippe, PINTO, Yigal M, ELLIOTT, Perry M, MOGENSEN, Jens, HERMANS-VAN AST, Johanna F, VAN DER KOOI, Anneke J, VAN TINTELEN, J. Peter, VAN DEN BERG, Maarten P, PILOTTO, Andrea, PASOTTI, Michele

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A Mutation in CALM1 Encoding Calmodulin in Familial Idiopathic Ventricular Fibrillation in Childhood and Adolescence von Marsman, Roos F., MD, Barc, Julien, PhD, Beekman, Leander, BSc, Alders, Marielle, PhD, Dooijes, Dennis, PhD, van den Wijngaard, Arthur, PhD, Ratbi, Ilham, MD, Sefiani, Abdelaziz, MD, PhD, Bhuiyan, Zahurul A., MD, PhD, Wilde, Arthur A.M., MD, PhD, Bezzina, Connie R., PhD

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Long-Term Clinical Outcomes of Subcutaneous Versus Transvenous Implantable Defibrillator Therapy von Brouwer, Tom F., MD, Yilmaz, Dilek, MD, Lindeboom, Robert, PhD, Buiten, Maurits S., MD, PhD, Olde Nordkamp, Louise R.A., MD, PhD, Schalij, Martin J., MD, PhD, Wilde, Arthur A., MD, PhD, van Erven, Lieselot, MD, PhD, Knops, Reinoud E., MD

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

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Risk stratification of sudden cardiac death: a review von Tfelt-Hansen, Jacob, Garcia, Rodrigue, Albert, Christine, Merino, Jose, Krahn, Andrew, Marijon, Eloi, Basso, Cristina, Wilde, Arthur A M, Haugaa, Kristina Hermann

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

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Permanent Leadless Cardiac Pacing: Results of the LEADLESS Trial von Reddy, Vivek Y, Knops, Reinoud E, Sperzel, Johannes, Miller, Marc A, Petru, Jan, Simon, Jaroslav, Sediva, Lucie, de Groot, Joris R, Tjong, Fleur V.Y, Jacobson, Peter, Ostrosff, Alan, Dukkipati, Srinivas R, Koruth, Jacob S, Wilde, Arthur A.M, Kautzner, Josef, Neuzil, Petr

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Flecainide Therapy Reduces Exercise-Induced Ventricular Arrhythmias in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia von van der Werf, Christian, MD, Kannankeril, Prince J., MD, MSCI, Sacher, Frederic, MD, Krahn, Andrew D., MD, Viskin, Sami, MD, Leenhardt, Antoine, MD, Shimizu, Wataru, MD, PhD, Sumitomo, Naokata, MD, Fish, Frank A., MD, Bhuiyan, Zahurul A., MD, PhD, Willems, Albert R., MD, PhD, van der Veen, Maurits J., MD, PhD, Watanabe, Hiroshi, MD, PhD, Laborderie, Julien, MD, Haïssaguerre, Michel, MD, Knollmann, Björn C., MD, PhD, Wilde, Arthur A.M., MD, PhD

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Genetic Testing for Long-QT Syndrome: Distinguishing Pathogenic Mutations From Benign Variants von KAPA, Suraj, TESTER, David J, SALISBURY, Benjamin A, HARRIS-KERR, Carole, PUNGLIYA, Manish S, ALDERS, Marielle, WILDE, Arthur A. M, ACKERMAN, Michael J

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Brugada syndrome and reduced right ventricular outflow tract conduction reserve: a final common pathway? von Behr, Elijah R, Ben-Haim, Yael, Ackerman, Michael J, Krahn, Andrew D, Wilde, Arthur A M

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Risk for Life-Threatening Cardiac Events in Patients With Genotype-Confirmed Long-QT Syndrome and Normal-Range Corrected QT Intervals von Goldenberg, Ilan, MD, Horr, Samuel, MA, Moss, Arthur J., MD, Lopes, Coeli M., PhD, Barsheshet, Alon, MD, McNitt, Scott, MS, Zareba, Wojciech, MD, PhD, Andrews, Mark L., BBA, Robinson, Jennifer L., MS, Locati, Emanuela H., MD, Ackerman, Michael J., MD, PhD, Benhorin, Jesaia, MD, Kaufman, Elizabeth S., MD, Napolitano, Carlo, MD, Platonov, Pyotr G., MD, PhD, Priori, Silvia G., MD, PhD, Qi, Ming, MD, Schwartz, Peter J., MD, Shimizu, Wataru, MD, PhD, Towbin, Jeffrey A., MD, Vincent, G. Michael, MD, Wilde, Arthur A.M., MD, PhD, Zhang, Li, MD

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The Response of the QT Interval to the Brief Tachycardia Provoked by Standing: A Bedside Test for Diagnosing Long QT Syndrome von VISKIN, Sami, POSTEMA, Pieter G, GLIKSON, Michael, STRASBERG, Boris, ANTZELEVITCH, Charles, WILDE, Arthur A. M, BHUIYAN, Zahurul A, ROSSO, Raphael, KALMAN, Jonathan M, VOHRA, Jitendra K, GUEVARA-VALDIVIA, Milton E, MARQUEZ, Manlio F, KOGAN, Evgeni, BELHASSEN, Bernard

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Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome von Nademanee, Koonlawee, MD, Raju, Hariharan, PhD, de Noronha, Sofia V., PhD, Papadakis, Michael, MD, Robinson, Laurence, MBBS, Rothery, Stephen, BSc, Makita, Naomasa, MD, Kowase, Shinya, MD, Boonmee, Nakorn, MD, Vitayakritsirikul, Vorapot, MD, Ratanarapee, Samrerng, MD, Sharma, Sanjay, MD, van der Wal, Allard C., MD, Christiansen, Michael, MD, Tan, Hanno L., MD, Wilde, Arthur A., MD, Nogami, Akihiko, MD, Sheppard, Mary N., MD, Veerakul, Gumpanart, MD, Behr, Elijah R., MD

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