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American Heart Journal|August 25, 2009
Prognosis among survivors of primary ventricular fibrillation in the percutaneous coronary intervention eraJonas S S G de Jong, Roos F Marsman, José P S Henriques, 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|June 28, 2023
Successful defibrillation testing in patients undergoing elective subcutaneous implantable cardioverter-defibrillator generator replacementJolien A de Veld, Shari Pepplinkhuizen, Willeke van der Stuijt, et al.
Circulation Research|January 11, 2003
A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstillW Antoinette Groenewegen, Mehran Firouzi, Connie R Bezzina, et al.
Journal of the American College of Cardiology|July 11, 2002
Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patientsJeroen P P Smits, Lars Eckardt, Vincent Probst, et al.
Neurocritical Care|October 9, 2009
Prevalence and characterization of ECG abnormalities after intracerebral hemorrhageMaurits D R van Bree, Yvo B W E M Roos, Ivo A C van der Bilt, et al.
Plos One|August 10, 2012
SCN5A mutations in Brugada syndrome are associated with increased cardiac dimensions and reduced contractilityFrans van Hoorn, Maria E Campian, Anje Spijkerboer, et al.
Circulation. Arrhythmia and Electrophysiology|October 8, 2009
Nodoventricular accessory pathways in PRKAG2-dependent familial preexcitation syndrome reveal a disorder in cardiac developmentHanno L Tan, Allard C van der Wal, Maria E Campian, et al.
Circulation|August 22, 2013
Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experienceNynke Hofman, Hanno L Tan, Mariëlle Alders, et al.
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