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Cardiac Electrophysiology Clinics|August 14, 2016
Role of Genetic Testing in Patients with Ventricular Arrhythmias in Apparently Normal HeartsNynke Hofman, Arthur A M WildeCurrent Opinion in Cardiology|February 19, 2010
Genetic testing in cardiovascular diseasesNynke Hofman, Irene van Langen, Arthur A M WildeFuture Cardiology|May 14, 2010
Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heartNynke Hofman, Laura T van Lochem, Arthur A M WildeJournal of Cardiovascular Electrophysiology|September 4, 2010
Sodium channelopathies: do we really understand what's going on?Pieter G Postema, Arend Mosterd, Nynke Hofman, et al.Nederlands Tijdschrift Voor Geneeskunde|October 4, 2011
[Premature sudden death--consider serious familial heart rhythm disturbances]Pieter G Postema, Imke Christiaans, Marielle Alders, et al.Journal of the American College of Cardiology|June 2, 2010
Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?Nynke Hofman, Hanno L Tan, Marielle Alders, et al.Pediatrics|October 3, 2007
Contribution of inherited heart disease to sudden cardiac death in childhoodNynke Hofman, Hanno L Tan, Sally-Ann Clur, et al.Circulation|July 7, 2005
Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relativesHanno L Tan, Nynke Hofman, Irene M van Langen, et al.Journal of Cardiovascular Electrophysiology|June 13, 2006
Diagnostic value of flecainide testing in unmasking SCN5A-related Brugada syndromePaola G Meregalli, Jan M Ruijter, Nynke Hofman, et al.Pediatric Cardiology|December 4, 2009
The role of the epinephrine test in the diagnosis and management of children suspected of having congenital long QT syndromeSally-Ann B Clur, Priya Chockalingam, Luc H Filippini, et al.Pageof 4