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Human Molecular Genetics|February 3, 2025
Sudden cardiac death, arrhythmogenic cardiomyopathy and intercalated disc pathology due to reduced filamin C protein levels: a matter of life and deathChristian Holtzhausen, Lorena Heil, Karin Klingel, et al.Science Advances|January 22, 2025
The deubiquitinase USP5 prevents accumulation of protein aggregates in cardiomyocytesYvonne Eibach, Silke Kreher, Mareike S Poetsch, et al.Journal of Cell Science|January 3, 2023
Meeting report - Desmosome dysfunction and disease: Alpine desmosome disease meetingVolker Spindler, Brenda Gerull, Kathleen J Green, et al.Genes|January 22, 2021
The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction CardiomyopathyOlga Kulikova, Andreas Brodehl, Anna Kiseleva, et al.Journal of Molecular and Cellular Cardiology|March 24, 2020
A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomyAndreas Brodehl, Jürgen Weiss, Jana Davina Debus, et al.European Journal of Heart Failure|July 3, 2026
A high proportion of children with severe cardiomyopathies show both myocarditis and genetic predispositionsHendrik Milting, Anna Gärtner, Caroline Wiebe, et al.Circulation. Heart Failure|March 2, 2012
Adipose tissue inflammation and adiponectin resistance in patients with advanced heart failure: correction after ventricular assist device implantationRaffay S Khan, Tomoko S Kato, Aalap Chokshi, et al.Circulation|May 16, 2012
Ventricular assist device implantation corrects myocardial lipotoxicity, reverses insulin resistance, and normalizes cardiac metabolism in patients with advanced heart failureAalap Chokshi, Konstantinos Drosatos, Faisal H Cheema, et al.Heart Failure Reviews|March 24, 2017
Redefining the role of biomarkers in heart failure trials: expert consensus documentFrank Kramer, Hani N Sabbah, James J Januzzi, et al.Heart Rhythm|November 17, 2015
Myocardial expression profiles of candidate molecules in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia compared to those with dilated cardiomyopathy and healthy controlsDeniz Akdis, Argelia Medeiros-Domingo, Anna Gaertner-Rommel, et al.Pageof 16