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Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|October 26, 2012
Brugada phenocopy: new terminology and proposed classificationAdrian Baranchuk, Timothy Nguyen, Min Hyung Ryu, et al.
European Heart Journal|March 11, 2021
Polymorphic ventricular tachycardia, ischaemic ventricular fibrillation, and torsade de pointes: importance of the QT and the coupling interval in the differential diagnosisRaphael Rosso, Aviram Hochstadt, Dana Viskin, et al.
Circulation. Arrhythmia and Electrophysiology|October 14, 2016
Ranolazine for Congenital Long-QT Syndrome Type III: Experimental and Long-Term Clinical DataEhud Chorin, Dan Hu, Charles Antzelevitch, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|April 18, 2026
Regional and Socioeconomic Disparities in the Diagnosis of Primary Electrical Diseases in a Universal Healthcare System: A Nationwide Danish StudyPriya Bhardwaj, Bo Gregers Winkel, Rasmus Bork Dinesen, et al.
Scientific Reports|June 27, 2024
Multimodal explainable artificial intelligence identifies patients with non-ischaemic cardiomyopathy at risk of lethal ventricular arrhythmiasMaarten Z H Kolk, Samuel Ruipérez-Campillo, Cornelis P Allaart, et al.
Heart Rhythm|October 8, 2018
A novel tool to evaluate the implant position and predict defibrillation success of the subcutaneous implantable cardioverter-defibrillator: The PRAETORIAN scoreAnne-Floor B E Quast, Sarah W E Baalman, Tom F Brouwer, et al.
Heart Rhythm|September 20, 2015
Implantable cardioverter-defibrillator harm in young patients with inherited arrhythmia syndromes: A systematic review and meta-analysis of inappropriate shocks and complicationsLouise R A Olde Nordkamp, Pieter G Postema, Reinoud E Knops, et al.
Journal of Cardiovascular Translational Research|April 10, 2015
Enhancing the Predictive Power of Mutations in the C-Terminus of the KCNQ1-Encoded Kv7.1 Voltage-Gated Potassium ChannelJamie D Kapplinger, Andrew S Tseng, Benjamin A Salisbury, et al.
Scientific Reports|August 4, 2016
hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalitiesChristiaan C Veerman, Isabella Mengarelli, Kaomei Guan, et al.
Progress in Biophysics and Molecular Biology|November 26, 2008
An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndromeZahurul A Bhuiyan, Tarek S Momenah, Ahmad S Amin, et al.
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