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Circulation. Arrhythmia and Electrophysiology|September 5, 2012
Epinephrine infusion in the evaluation of unexplained cardiac arrest and familial sudden death: from the cardiac arrest survivors with preserved Ejection Fraction RegistryAndrew D Krahn, Jeffrey S Healey, Vijay S Chauhan, et al.
Circulation. Arrhythmia and Electrophysiology|September 17, 2016
Cardiac Abnormalities in First-Degree Relatives of Unexplained Cardiac Arrest Victims: A Report From the Cardiac Arrest Survivors With Preserved Ejection Fraction RegistryChristian Steinberg, Gareth J Padfield, Jean Champagne, et al.
Cardiovascular Research|May 16, 2022
Spatial transcriptomics unveils ZBTB11 as a regulator of cardiomyocyte degeneration in arrhythmogenic cardiomyopathyCornelis J Boogerd, Grégory P A Lacraz, Ábel Vértesy, et al.
Nature Genetics|October 19, 2004
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathyBrenda Gerull, Arnd Heuser, Thomas Wichter, et al.
Frontiers in Cardiovascular Medicine|May 31, 2023
Ultra-high field cardiac MRI in large animals and humans for translational cardiovascular researchLaura M Schreiber, David Lohr, Steffen Baltes, et al.
Circulation. Cardiovascular Genetics|June 11, 2017
Genetic Testing in the Evaluation of Unexplained Cardiac Arrest: From the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry)Greg Mellor, Zachary W M Laksman, Rafik Tadros, et al.
International Journal of Molecular Sciences|July 2, 2021
The Double Mutation DSG2-p.S363X and TBX20-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case ReportRoman Myasnikov, Andreas Brodehl, Alexey Meshkov, et al.
Journal of Clinical Medicine|April 3, 2020
Desminopathy: Novel Desmin Variants, a New Cardiac Phenotype, and Further Evidence for Secondary Mitochondrial DysfunctionMiloš Kubánek, Tereza Schimerová, Lenka Piherová, et al.
EMBO Molecular Medicine|March 12, 2015
Antisense-mediated exon skipping: a therapeutic strategy for titin-based dilated cardiomyopathyMichael Gramlich, Luna Simona Pane, Qifeng Zhou, et al.
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