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European Journal of Heart Failure|January 26, 2013
Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experienceKarin Y van Spaendonck-Zwarts, Ingrid A W van Rijsingen, Maarten P van den Berg, et al.
Advances in Wound Care|August 20, 2025
Management of Diabetic Wounds: Expert Panel Consensus StatementHenry C Hsia, Elof Eriksson, Geoffrey C Gurtner, et al.
European Journal of Heart Failure|June 19, 2019
Definition and treatment of arrhythmogenic cardiomyopathy: an updated expert panel reportPerry M Elliott, Aris Anastasakis, Angeliki Asimaki, et al.
European Heart Journal|September 3, 2025
Clinical care of family members of patients with dilated cardiomyopathyJob A J Verdonschot, Juan Pablo Kaski, Folkert W Asselbergs, et al.
Journal of the American College of Cardiology|January 28, 2012
Risk factors for malignant ventricular arrhythmias in lamin a/c mutation carriers a European cohort studyIngrid A W van Rijsingen, Eloisa Arbustini, Perry M Elliott, et al.
Heart Rhythm|November 3, 2009
Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES geneJ Peter van Tintelen, Isabelle C Van Gelder, Angeliki Asimaki, et al.
Circulation. Genomic and Precision Medicine|August 7, 2019
Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De NovoFreyja H M van Lint, Brittney Murray, Crystal Tichnell, et al.
The New Phytologist|May 12, 2010
Nodulation and nitrogen fixation by Mimosa spp. in the Cerrado and Caatinga biomes of BrazilFábio Bueno Dos Reis, Marcelo F Simon, Eduardo Gross, et al.
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