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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An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome von Adler, Arnon, Novelli, Valeria, Amin, Ahmad S., Abiusi, Emanuela, Care, Melanie, Nannenberg, Eline A., Feilotter, Harriet, Amenta, Simona, Mazza, Daniela, Bikker, Hennie, Sturm, Amy C., Garcia, John, Ackerman, Michael J., Hershberger, Raymond E., Perez, Marco V., Zareba, Wojciech, Ware, James S., Wilde, Arthur A.M., Gollob, Michael H.

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Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death von Walsh, Roddy, Adler, Arnon, Amin, Ahmad S, Abiusi, Emanuela, Care, Melanie, Bikker, Hennie, Amenta, Simona, Feilotter, Harriet, Nannenberg, Eline A, Mazzarotto, Francesco, Trevisan, Valentina, Garcia, John, Hershberger, Ray E, Perez, Marco V, Sturm, Amy C, Ware, James S, Zareba, Wojciech, Novelli, Valeria, Wilde, Arthur A M, Gollob, Michael H

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RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium Handling von van den Hoogenhof, Maarten M.G, Beqqali, Abdelaziz, Amin, Ahmad S, van der Made, Ingeborg, Aufiero, Simona, Khan, Mohsin A.F, Schumacher, Cees A, Jansweijer, Joeri A, van Spaendonck-Zwarts, Karin Y, Remme, Carol Ann, Backs, Johannes, Verkerk, Arie O, Baartscheer, Antonius, Pinto, Yigal M, Creemers, Esther E

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Predicting cardiac electrical response to sodium-channel blockade and Brugada syndrome using polygenic risk scores von Tadros, Rafik, Tan, Hanno L, el Mathari, Sulayman, Kors, Jan A, Postema, Pieter G, Lahrouchi, Najim, Beekman, Leander, Radivojkov-Blagojevic, Milena, Amin, Ahmad S, Meitinger, Thomas, Tanck, Michael W, Wilde, Arthur A, Bezzina, Connie R

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Drugs and Brugada syndrome patients: Review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org) von Postema, Pieter G., MD, Wolpert, Christian, MD, Amin, Ahmad S., MD, Probst, Vincent, MD, PhD, Borggrefe, Martin, MD, PhD, Roden, Dan M., MD, Priori, Silvia G., MD, PhD, Tan, Hanno L., MD, PhD, Hiraoka, Masayasu, MD, PhD, Brugada, Josep, MD, PhD, Wilde, Arthur A.M., MD, PhD

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Improving electrocardiogram-based detection of rare genetic heart disease using transfer learning: An application to phospholamban p.Arg14del mutation carriers von Lopes, Ricardo R., Bleijendaal, Hidde, Ramos, Lucas A., Verstraelen, Tom E., Amin, Ahmad S., Wilde, Arthur A.M., Pinto, Yigal M., de Mol, Bas A.J.M., Marquering, Henk A.

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Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand von Makarawate, Pattarapong, Glinge, Charlotte, Khongphatthanayothin, Apichai, Walsh, Roddy, Mauleekoonphairoj, John, Amnueypol, Montawatt, Prechawat, Somchai, Wongcharoen, Wanwarang, Krittayaphong, Rungroj, Anannab, Alisara, Lichtner, Peter, Meitinger, Thomas, Tjong, Fleur V.Y., Lieve, Krystien V.V., Amin, Ahmad S., Sahasatas, Dujdao, Ngarmukos, Tachapong, Wichadakul, Duangdao, Payungporn, Sunchai, Sutjaporn, Boosamas, Wandee, Pharawee, Poovorawan, Yong, Tfelt-Hansen, Jacob, Tanck, Michael W.T., Tadros, Rafik, Wilde, Arthur A.M., Bezzina, Connie R., Veerakul, Gumpanart, Nademanee, Koonlawee

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Long QT syndrome: beyond the causal mutation von Amin, Ahmad S., Pinto, Yigal M., Wilde, Arthur A. M.

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Importance of exercise stress testing in evaluation of unexplained cardiac arrest survivor von Bergeman, Auke T., Robyns, Tomas, Amin, Ahmad S., Wilde, Arthur A. M., van der Werf, Christian

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The Prognostic Significance of Fever-Induced Brugada Syndrome von Mizusawa, Yuka, MD, Morita, Hiroshi, MD, PhD, Adler, Arnon, MD, PhD, Havakuk, Ofer, MD, Thollet, Aurélie, PhD, Maury, Philippe, MD, Wang, Dao W., MD, PhD, Hong, Kui, MD, PhD, Gandjbakhch, Estelle, MD, PhD, Sacher, Frédéric, MD, PhD, Hu, Dan, MD, PhD, Amin, Ahmad S., MD, PhD, Lahrouchi, Najim, MD, Tan, Hanno L., MD, PhD, Antzelevitch, Charles, PhD, Probst, Vincent, MD, PhD, Viskin, Sami, MD, Wilde, Arthur A.M., MD, PhD

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SCN5A -related dilated cardiomyopathy: What do we know? von Amin, Ahmad S., MD, PhD

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Cardiac ion channels in health and disease von Amin, Ahmad S., MD, Tan, Hanno L., MD, PhD, Wilde, Arthur A.M., MD, PhD

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Disease Modifiers of Inherited SCN5A Channelopathy von Verkerk, Arie O, Amin, Ahmad S, Remme, Carol Ann

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Left Axis Deviation in Brugada Syndrome: Vectorcardiographic Evaluation during Ajmaline Provocation Testing Reveals Additional Depolarization Abnormalities von Van der Ree, Martijn H., Vendrik, Jeroen, Kors, Jan A., Amin, Ahmad S., Wilde, Arthur A. M., Tan, Hanno L., Postema, Pieter G.

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SCN5a overlap syndromes—This episode: Long QT syndrome type 3 meets multifocal ectopic Purkinje-related premature contractions von Amin, Ahmad S.

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Clinical Spectrum of SCN5A Mutations: Long QT Syndrome, Brugada Syndrome, and Cardiomyopathy von Wilde, Arthur A M, Amin, Ahmad S

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Exercise-Induced ECG Changes in Brugada Syndrome von Amin, Ahmad S, de Groot, Elisabeth A.A, Ruijter, Jan M, Wilde, Arthur A.M, Tan, Hanno L

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Diagnosis of Brugada Syndrome With a Sodium-Channel-Blocker Test: Who Should Be Tested? Who Should Not? von Viskin, Sami, Chorin, Ehud, Rosso, Raphael, Amin, Ahmad S, Wilde, Arthur A

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Use, misuse, and pitfalls of the drug challenge test in the diagnosis of the Brugada syndrome von Wilde, Arthur A M, Amin, Ahmad S, Morita, Hiroshi, Tadros, Rafik

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