Inherited cardiac arrhythmias
Schwartz, Peter J., Ackerman, Michael J., Antzelevitch, Charles, Bezzina, Connie R., Borggrefe, Martin, Cuneo, Bettina F., Wilde, Arthur A. M.
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Epidemiology of inherited arrhythmias
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Published in Nature reviews cardiology (01.04.2020)
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Published in Journal of the American College of Cardiology (31.01.2012)
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A Mutation in CALM1 Encoding Calmodulin in Familial Idiopathic Ventricular Fibrillation in Childhood and Adolescence
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Flecainide Therapy Reduces Exercise-Induced Ventricular Arrhythmias in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
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Published in Journal of the American College of Cardiology (31.05.2011)
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Multimodal explainable artificial intelligence identifies patients with non-ischaemic cardiomyopathy at risk of lethal ventricular arrhythmias
Kolk, Maarten Z. H., Ruipérez-Campillo, Samuel, Allaart, Cornelis P., Wilde, Arthur A. M., Knops, Reinoud E., Narayan, Sanjiv M., Tjong, Fleur V. Y.
Published in Scientific reports (27.06.2024)
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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
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Published in Journal of the American College of Cardiology (04.05.2010)
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Incidence, Causes, and Outcomes of Out-of-Hospital Cardiac Arrest in Children: A Comprehensive, Prospective, Population-Based Study in the Netherlands
BARDAI, Abdennasser, BERDOWSKI, Jocelyn, VAN DER WERF, Christian, BLOM, Marieke T, CEELEN, Manon, VAN LANGEN, Irene M, TIJSSEN, Jan G. P, WILDE, Arthur A. M, KOSTER, Rudolph W, TAN, Hanno L
Published in Journal of the American College of Cardiology (03.05.2011)
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Risk for Life-Threatening Cardiac Events in Patients With Genotype-Confirmed Long-QT Syndrome and Normal-Range Corrected QT Intervals
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
Published in Journal of the American College of Cardiology (04.01.2011)
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The development and validation of an easy to use automatic QT-interval algorithm
Hermans, Ben J M, Vink, Arja S, Bennis, Frank C, Filippini, Luc H, Meijborg, Veronique M F, Wilde, Arthur A M, Pison, Laurent, Postema, Pieter G, Delhaas, Tammo
Published in PloS one (01.09.2017)
Published in PloS one (01.09.2017)
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Prevalence of Mitral Annulus Disjunction and Mitral Valve Prolapse in Patients With Idiopathic Ventricular Fibrillation
Groeneveld, Sanne A., Kirkels, Feddo P., Cramer, Maarten J., Evertz, Reinder, Haugaa, Kristina H., Postema, Pieter G., Prakken, Niek H. J., Teske, Arco J., Wilde, Arthur A. M., Velthuis, Birgitta K., Nijveldt, Robin, Hassink, Rutger J.
Published in Journal of the American Heart Association (16.08.2022)
Published in Journal of the American Heart Association (16.08.2022)
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SCN5A mutations in Brugada syndrome are associated with increased cardiac dimensions and reduced contractility
van Hoorn, Frans, Campian, Maria E, Spijkerboer, Anje, Blom, Marieke T, Planken, R Nils, van Rossum, Albert C, de Bakker, Jacques M T, Wilde, Arthur A M, Groenink, Maarten, Tan, Hanno L
Published in PloS one (02.08.2012)
Published in PloS one (02.08.2012)
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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
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Published in Circulation (New York, N.Y.) (15.05.2007)
Published in Circulation (New York, N.Y.) (15.05.2007)
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Wilde, Arthur A M, Amin, Ahmad S, Postema, Pieter G
Published in Heart (British Cardiac Society) (01.03.2022)
Published in Heart (British Cardiac Society) (01.03.2022)
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Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner
AMIN, Ahmad S, GIUDICESSI, John R, MÜLLER, Martina, WIJNEN, Wino J, TAN, Hanno L, BEZZINA, Connie R, CREEMERS, Esther E, WILDE, Arthur A. M, ACKERMAN, Michael J, PINTO, Yigal M, TIJSEN, Anke J, SPANJAART, Anne M, RECKMAN, Yolan J, KLEMENS, Christine A, TANCK, Michael W, KAPPLINGER, Jamie D, HOFMAN, Nynke, SINNER, Moritz F
Published in European heart journal (01.03.2012)
Published in European heart journal (01.03.2012)
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Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes
Behr, Elijah R, Ritchie, Marylyn D, Tanaka, Toshihiro, Kääb, Stefan, Crawford, Dana C, Nicoletti, Paola, Floratos, Aris, Sinner, Moritz F, Kannankeril, Prince J, Wilde, Arthur A M, Bezzina, Connie R, Schulze-Bahr, Eric, Zumhagen, Sven, Guicheney, Pascale, Bishopric, Nanette H, Marshall, Vanessa, Shakir, Saad, Dalageorgou, Chrysoula, Bevan, Steve, Jamshidi, Yalda, Bastiaenen, Rachel, Myerburg, Robert J, Schott, Jean-Jacques, Camm, A John, Steinbeck, Gerhard, Norris, Kris, Altman, Russ B, Tatonetti, Nicholas P, Jeffery, Steve, Kubo, Michiaki, Nakamura, Yusuke, Shen, Yufeng, George, Jr, Alfred L, Roden, Dan M
Published in PloS one (06.11.2013)
Published in PloS one (06.11.2013)
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