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European Heart Journal|January 21, 2016
Genotype impacts survival in Marfan syndromeRomy Franken, Maarten Groenink, Vivian de Waard, et al.
The Annals of Thoracic Surgery|April 25, 2006
Favorable long-term outcome of Maze surgery in patients with lone atrial fibrillationMartin E W Hemels, Youlan L Gu, Anton E Tuinenburg, et al.
Journal of the American College of Cardiology|January 24, 2015
The risk for type B aortic dissection in Marfan syndromeAlexander W den Hartog, Romy Franken, Aeilko H Zwinderman, et al.
American Journal of Medical Genetics. Part A|March 31, 2012
Diagnostic yield in adults screened at the Marfan outpatient clinic using the 1996 and 2010 Ghent nosologiesJan J J Aalberts, Chris H L Thio, Agnes G Schuurman, et al.
Heart Rhythm|June 10, 2022
Value of genetic testing in the diagnosis and risk stratification of arrhythmogenic right ventricular cardiomyopathyRemco de Brouwer, Laurens P Bosman, Sophia Gripenstedt, et al.
Circulation|May 12, 2010
Peripartum cardiomyopathy as a part of familial dilated cardiomyopathyKarin Y van Spaendonck-Zwarts, J Peter van Tintelen, Dirk J van Veldhuisen, et al.
Psychosomatic Medicine|November 27, 2004
Prognostic association of depression following myocardial infarction with mortality and cardiovascular events: a meta-analysisJoost P van Melle, Peter de Jonge, Titia A Spijkerman, et al.
International Journal of Cardiology|May 1, 2018
SCN5A mutation type and topology are associated with the risk of ventricular arrhythmia by sodium channel blockersAhmad S Amin, Yolan J Reckman, Elena Arbelo, et al.
Human Mutation|July 2, 2009
A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathyPaul A van der Zwaag, Jan D H Jongbloed, Maarten P van den Berg, et al.
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