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Nature Reviews. Cardiology|May 23, 2025
Gene therapy for cardiac arrhythmiasSahej Bains, John R Giudicessi, Katja E Odening, et al.Mayo Clinic Proceedings|January 17, 2003
Catecholamine-induced T-wave lability in congenital long QT syndrome: a novel phenomenon associated with syncope and cardiac arrestJan Nemec, Joseph B Hejlik, Win-Kuang Shen, et al.The American Journal of Cardiology|September 16, 2003
Syncope in children and adolescents and the congenital long QT syndromeAnant Khositseth, Matthew W Martinez, David J Driscoll, et al.Heart Rhythm|May 27, 2009
Left cardiac sympathetic denervation for the treatment of long QT syndrome and catecholaminergic polymorphic ventricular tachycardia using video-assisted thoracic surgeryChristopher A Collura, Jonathan N Johnson, Christopher Moir, et al.American Journal of Physiology. Heart and Circulatory Physiology|August 12, 2009
GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5ACarmen R Valdivia, Kazuo Ueda, Michael J Ackerman, et al.Pediatric Cardiology|August 24, 2011
Call for a sudden cardiac death registry: should reporting of sudden cardiac death be mandatory?Robert M Campbell, Stuart Berger, Michael J Ackerman, et al.Pediatric Cardiology|November 19, 2010
Clinical spectrum in a family with tropomyosin-mediated hypertrophic cardiomyopathy and sudden death in childhoodMajd Makhoul, Michael J Ackerman, Dianne L Atkins, et al.Heart Rhythm|May 14, 2020
Phenotype-guided whole genome analysis in a patient with genetically elusive long QT syndrome yields a novel TRDN-encoded triadin pathogenetic substrate for triadin knockout syndrome and reveals a novel primate-specific cardiac TRDN transcriptDaniel J Clemens, David J Tester, Isabelle Marty, et al.Journal of the American College of Cardiology|July 31, 2021
Return-to-Play for Athletes With Long QT Syndrome or Genetic Heart Diseases Predisposing to Sudden DeathKathryn E Tobert, J Martijn Bos, Ramin Garmany, et al.Physiological Genomics|November 28, 2002
A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutationBin Ye, Carmen R Valdivia, Michael J Ackerman, et al.Pageof 73