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International Journal of Cardiology|March 7, 2017
Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillationKrystien V Lieve, Arie O Verkerk, Svitlana Podliesna, et al.
Journal of the American Heart Association|July 26, 2017
Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease-Causing MutationChristiaan C Veerman, Isabella Mengarelli, Elisabeth M Lodder, et al.
Circulation|January 12, 2005
Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndromeLars Eckardt, Vincent Probst, Jeroen P P Smits, et al.
Circulation Research|May 3, 2008
A gain-of-function TBX5 mutation is associated with atypical Holt-Oram syndrome and paroxysmal atrial fibrillationAlex V Postma, Judith B A van de Meerakker, Inge B Mathijssen, et al.
Journal of Molecular and Cellular Cardiology|May 10, 2003
Na+ channel mutation leading to loss of function and non-progressive cardiac conduction defectsLucas J Herfst, Franck Potet, Connie R Bezzina, et al.
BMJ Open Sport & Exercise Medicine|October 25, 2021
Cardiac abnormalities in athletes after SARS-CoV-2 infection: a systematic reviewJuliette C van Hattum, Jessica L Spies, Sjoerd M Verwijs, et al.
European Journal of Human Genetics : EJHG|December 14, 2023
Are disease-specific patient-reported outcomes measures (PROMs) used in cardiogenetics? A systematic reviewSaar van Pottelberghe, Nina Kupper, Esther Scheirlynck, et al.
Journal of Cardiovascular Electrophysiology|June 4, 2009
Mutations in conserved amino acids in the KCNQ1 channel and risk of cardiac events in type-1 long-QT syndromeChristian Jons, Arthur J Moss, Coeli M Lopes, et al.
Journal of Electrocardiology|April 1, 2026
Mobile ECG for QTc assessment in cLQTS: A step toward remote monitoringNicole J van Steijn, Auke T Bergeman, Christian van der Werf, et al.
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