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International Journal of Cardiology|June 1, 2015
Inappropriate shocks in the subcutaneous ICD: Incidence, predictors and managementLouise R A Olde Nordkamp, Tom F Brouwer, Craig Barr, et al.
Circulation. Cardiovascular Genetics|March 17, 2011
A complex double deletion in LMNA underlies progressive cardiac conduction disease, atrial arrhythmias, and sudden deathRoos F Marsman, Abdennasser Bardai, Alex V Postma, et al.
European Journal of Human Genetics : EJHG|December 17, 2015
Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunctionHideki Itoh, Myriam Berthet, Véronique Fressart, et al.
Journal of the American College of Cardiology|April 18, 2015
Chronic performance of a leadless cardiac pacemaker: 1-year follow-up of the LEADLESS trialReinoud E Knops, Fleur V Y Tjong, Petr Neuzil, et al.
Journal of Cardiovascular Development and Disease|November 24, 2023
TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without AortopathyManal Alaamery, Nour Albesher, Fahad Alhabshan, et al.
Circulation Research|June 23, 2017
The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical HeterogeneityChristiaan C Veerman, Svitlana Podliesna, Rafik Tadros, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|July 20, 2023
Manual vs. automatic assessment of the QT-interval and corrected QTBenjamin Neumann, A Suzanne Vink, Ben J M Hermans, et al.
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