Showing results (591-600 of 723) with videos related to
Sort By:
Pageof 73
Circulation. Arrhythmia and Electrophysiology|September 8, 2022
Substrate Characterization and Outcomes of Catheter Ablation of Ventricular Arrhythmias in Patients With Mitral Annular DisjunctionFatima M Ezzeddine, Konstantinos C Siontis, John Giudicessi, et al.Circulation. Arrhythmia and Electrophysiology|December 7, 2018
Safety of Sports for Young Patients With Implantable Cardioverter-Defibrillators: Long-Term Results of the Multinational ICD Sports RegistryElizabeth Vickers Saarel, Ian Law, Charles I Berul, et al.Journal of Imaging|May 27, 2022
Deep Neural Network for Cardiac Magnetic Resonance Image SegmentationDavid Chen, Huzefa Bhopalwala, Nakeya Dewaswala, et al.Circulation|November 7, 2007
The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratificationLia Crotti, Carla Spazzolini, Peter J Schwartz, et al.Circulation|May 2, 2007
Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 geneArthur J Moss, Wataru Shimizu, Arthur A M Wilde, et al.Circulation|June 28, 2024
Therapeutic Efficacy of Mexiletine for Long QT Syndrome Type 2: Evidence From Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes, Transgenic Rabbits, and PatientsLia Crotti, Raquel Neves, Federica Dagradi, et al.Journal of Neuropathology and Experimental Neurology|March 18, 2011
Dysferlin, annexin A1, and mitsugumin 53 are upregulated in muscular dystrophy and localize to longitudinal tubules of the T-system with stretchLeigh B Waddell, Frances A Lemckert, Xi F Zheng, et al.JAMA Cardiology|April 4, 2019
Development and Validation of a Deep-Learning Model to Screen for Hyperkalemia From the ElectrocardiogramConner D Galloway, Alexander V Valys, Jacqueline B Shreibati, et al.Circulation|October 31, 2007
Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmiasBarry London, Michael Michalec, Haider Mehdi, et al.European Heart Journal|June 14, 2020
An autoantibody profile detects Brugada syndrome and identifies abnormally expressed myocardial proteinsDiptendu Chatterjee, Maurizio Pieroni, Meena Fatah, et al.Pageof 73