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American Journal of Physiology. Heart and Circulatory Physiology|July 18, 2020
Desmin is essential for the structure and function of the sinoatrial node: implications for increased arrhythmogenesisManolis Mavroidis, Nikolaos C Athanasiadis, Pavlos Rigas, et al.
International Journal of Molecular Sciences|September 23, 2022
Towards a Better Understanding of Genotype-Phenotype Correlations and Therapeutic Targets for Cardiocutaneous Genes: The Importance of Functional Studies above PredictionMathilde C S C Vermeer, Daniela Andrei, Luisa Marsili, et al.
European Journal of Heart Failure|March 3, 2015
A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle-specific genesMagdalena Harakalova, Gijs Kummeling, Arjan Sammani, et al.
Open Heart|October 22, 2014
Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathyMarijke Wasielewski, Karin Y van Spaendonck-Zwarts, Nico-Derk L Westerink, et al.
Journal of the American College of Cardiology|July 19, 2005
Developmental aspects of long QT syndrome type 3 and Brugada syndrome on the basis of a single SCN5A mutation in childhoodGertie C M Beaufort-Krol, Maarten P van den Berg, Arthur A M Wilde, et al.
Heart Rhythm|February 7, 2018
Predicting arrhythmic risk in arrhythmogenic right ventricular cardiomyopathy: A systematic review and meta-analysisLaurens P Bosman, Arjan Sammani, Cynthia A James, 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.
European Journal of Medical Genetics|August 28, 2007
Two related Dutch families with a clinically variable presentation of cardioskeletal myopathy caused by a novel S13F mutation in the desmin geneJorieke E H Bergman, Hermine E Veenstra-Knol, Anthonie J van Essen, et al.
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