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Heart Rhythm O2|June 11, 2021
Diagnostic accuracy of the response to the brief tachycardia provoked by standing in children suspected for long QT syndromeArja S Vink, Ben J M Hermans, Joana Pimenta, et al.
Journal of the American Heart Association|July 8, 2023
Diagnostic Accuracy of the Standing Test in Adults Suspected for Congenital Long-QT SyndromeArja S Vink, Ben J M Hermans, Jean-Luc Q Hooglugt, et al.
Science Translational Medicine|April 1, 2011
Use of mutant-specific ion channel characteristics for risk stratification of long QT syndrome patientsChristian Jons, Jin O-Uchi, Arthur J Moss, 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.
Circulation|May 2, 2007
Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 geneArthur J Moss, Wataru Shimizu, Arthur A M Wilde, 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|August 5, 2021
Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association SurveyElijah R Behr, Chiara Scrocco, Arthur A M Wilde, et al.
Circulation|December 21, 2018
Determination and Interpretation of the QT IntervalArja Suzanne Vink, Benjamin Neumann, Krystien V V Lieve, 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|May 23, 2019
Incidence and predictors of implantable cardioverter-defibrillator therapy and its complications in idiopathic ventricular fibrillation patientsLennart J Blom, Marloes Visser, Imke Christiaans, et al.
Journal of the American College of Cardiology|November 21, 2009
Genotype-phenotype aspects of type 2 long QT syndromeWataru Shimizu, Arthur J Moss, Arthur A M Wilde, et al.
European Heart Journal|December 27, 2011
Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific mannerAhmad S Amin, John R Giudicessi, Anke J Tijsen, et al.
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