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The American Journal of Medicine|December 19, 2023
Prevalence of Cardiac Sarcoidosis in Middle-Aged Adults Diagnosed with High-Grade Atrioventricular BlockLeonid Maizels, Mahmoud Mansour, Arsalan Abu-Much, et al.CJC Open|July 18, 2024
Absence of Pericarditis Recurrence in Rilonacept-Treated Patients With COVID-19 and SARS-CoV-2 Vaccination: Results From the RHAPSODY Long-term ExtensionAntonio Brucato, Lucia Trotta, Michael Arad, et al.Journal of the American Heart Association|August 30, 2021
<i>LAMP2</i> Cardiomyopathy: Consequences of Impaired Autophagy in the HeartRonny Alcalai, Michael Arad, Hiroko Wakimoto, et al.Heart Rhythm|June 25, 2011
Postpacing abnormal repolarization in catecholaminergic polymorphic ventricular tachycardia associated with a mutation in the cardiac ryanodine receptor geneEyal Nof, Bernard Belhassen, Michael Arad, et al.Annals of Clinical and Translational Neurology|February 11, 2023
Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic featuresAmir Dori, Michael Arad, Yishay Wasserstrum, et al.International Journal of Cardiology|June 14, 2020
Reduction in Filamin C transcript is associated with arrhythmogenic cardiomyopathy in Ashkenazi JewsShimrit Oz, Hagith Yonath, Leonid Visochyk, et al.The Journal of Clinical Investigation|April 14, 2007
Aberrant activation of AMP-activated protein kinase remodels metabolic network in favor of cardiac glycogen storageIvan Luptak, Mei Shen, Huamei He, et al.Clinical Chemistry and Laboratory Medicine|September 25, 2023
Amino acid sequence homology of monoclonal serum free light chain dimers and tissue deposited light chains in AL amyloidosis: a pilot studyRivka Goldis, Batia Kaplan, Michael Arad, et al.European Heart Journal|September 9, 2010
Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial DiseasesPhilippe Charron, Michael Arad, Eloisa Arbustini, et al.Journal of Cellular and Molecular Medicine|January 9, 2019
Electrophysiological abnormalities in induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patientsBinyamin Eisen, Ronen Ben Jehuda, Ashley J Cuttitta, et al.Pageof 15