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

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

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

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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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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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The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology von Veerman, Christiaan C., Wilde, Arthur A.M., Lodder, Elisabeth M.

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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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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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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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Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene von MOSS, Arthur J, SHIMIZU, Wataru, HOFMAN, Nynke, SETH, Rahul, KAMAKURA, Shiro, MIYAMOTO, Yoshihiro, GOLDENBERG, Ilan, ANDREWS, Mark L, MCNITT, Scott, WILDE, Arthur A. M, TOWBIN, Jeffrey A, ZAREBA, Wojciech, ROBINSON, Jennifer L, MING QI, VINCENT, G. Michael, ACKERMAN, Michael J, KAUFMAN, Elizabeth S

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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 RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative,... von Medeiros-Domingo, Argelia, Bhuiyan, Zahurul A, Tester, David J, Hofman, Nynke, Bikker, Hennie, van Tintelen, J Peter, Mannens, Marcel M A M, Wilde, Arthur A M, Ackerman, Michael J

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Heritability in genetic heart disease: the role of genetic background von Jansweijer, Joeri A, van Spaendonck-Zwarts, Karin Y, Tanck, Michael W T, van Tintelen, J Peter, Christiaans, Imke, van der Smagt, Jasper J, Vermeer, Alexa M C, Bos, J Martijn, Moss, Arthur J, Swan, Heikki, Priori, Sylvia G, Rydberg, Annika, Tfelt-Hansen, Jacob, Ackerman, Michael J, Olivotto, Iacopo, Charron, Philippe, Gimeno, Juan R, van den Berg, Maarten P, Wilde, Arthur AM, Pinto, Yigal M

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The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity von Veerman, Christiaan C, Podliesna, Svitlana, Tadros, Rafik, Lodder, Elisabeth M, Mengarelli, Isabella, de Jonge, Berend, Beekman, Leander, Barc, Julien, Wilders, Ronald, Wilde, Arthur A.M, Boukens, Bastiaan J, Coronel, Ruben, Verkerk, Arie O, Remme, Carol, Bezzina, Connie R

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A New ECG Sign of Proximal LAD Occlusion von Wilde, Arthur A.M, de Winter, Robbert J, Wellens, Hein J.J, Verouden, Niels J.W

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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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Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2: Higher Recurrence of Events Under Metoprolol von CHOCKALINGAM, Priya, CROTTI, Lia, RYDBERG, Annika, CLUR, Sally-Ann B, FISCHER, Markus, DEN HEUVEL, Freek Van, KAAB, Stefan, BLOM, Nico A, ACKERMAN, Michael J, SCHWARTZ, Peter J, WILDE, Arthur A. M, GIRARDENGO, Giulia, JOHNSON, Jonathan N, HARRIS, Katy M, DER HEIJDEN, Jeroen F. Van, HAUER, Richard N. W, BECKMANN, Britt M, SPAZZOLINI, Carla, RORDORF, Roberto

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Sudden cardiac death a matter of genes? von Wilde, Arthur AM

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Genotype-Phenotype Aspects of Type 2 Long QT Syndrome von Shimizu, Wataru, MD, PhD, Moss, Arthur J., MD, Wilde, Arthur A.M., MD, PhD, Towbin, Jeffrey A., MD, Ackerman, Michael J., MD, PhD, January, Craig T., MD, PhD, Tester, David J., BS, Zareba, Wojciech, MD, PhD, Robinson, Jennifer L., MS, Qi, Ming, PhD, Vincent, G. Michael, MD, Kaufman, Elizabeth S., MD, Hofman, Nynke, MSc, Noda, Takashi, MD, PhD, Kamakura, Shiro, MD, PhD, Miyamoto, Yoshihiro, MD, PhD, Shah, Samit, BA, Amin, Vinit, MA, Goldenberg, Ilan, MD, Andrews, Mark L., BBA, McNitt, Scott, MS

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Chronic performance of a leadless cardiac pacemaker: 1-year follow-up of the LEADLESS trial von Knops, Reinoud E, Tjong, Fleur V Y, Neuzil, Petr, Sperzel, Johannes, Miller, Marc A, Petru, Jan, Simon, Jaroslav, Sediva, Lucie, de Groot, Joris R, Dukkipati, Srinivas R, Koruth, Jacob S, Wilde, Arthur A M, Kautzner, Josef, Reddy, Vivek Y

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