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Circulation|May 26, 2004
Mutation in the KCNQ1 gene leading to the short QT-interval syndromeChloé Bellocq, Antoni C G van Ginneken, Connie R Bezzina, et al.
Circulation|January 18, 2006
Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conductionConnie R Bezzina, Wataru Shimizu, Ping Yang, et al.
Pediatric Cardiology|May 24, 2018
A Potential Diagnostic Approach for Foetal Long-QT Syndrome, Developed and Validated in ChildrenArja Suzanne Vink, Irene M Kuipers, Rianne H A C M De Bruin-Bon, et al.
International Journal of Cardiology|June 9, 2020
Improving the care for female subcutaneous ICD patients: A qualitative study of gender-specific issuesWilleke van der Stuijt, Anne-Floor B E Quast, Sarah W E Baalman, et al.
Cardiovascular Digital Health Journal|January 2, 2023
Accuracy and clinical relevance of the single-lead Apple Watch electrocardiogram to identify atrial fibrillationShari Pepplinkhuizen, Wiert F Hoeksema, Willeke van der Stuijt, et al.
Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|April 17, 2013
Electrocardiographic P wave changes after thoracoscopic pulmonary vein isolation for atrial fibrillationMartina Nassif, Sébastien P J Krul, Antoine H G Driessen, et al.
Journal of Cardiovascular Electrophysiology|August 2, 2007
A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22Zahurul A Bhuiyan, Mohamed A Hamdan, Eman T A Shamsi, et al.
Heart Rhythm|August 14, 2012
The diagnostic and therapeutic aspects of loss-of-function cardiac sodium channelopathies in childrenPriya Chockalingam, Sally-Ann B Clur, Johannes M P J Breur, et al.
Heart Rhythm|September 1, 2009
Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic testJamie D Kapplinger, David J Tester, Benjamin A Salisbury, et al.
Heart Rhythm|June 9, 2007
Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohortTamara T Koopmann, Leander Beekman, Marielle Alders, et al.
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