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Heart Rhythm|February 2, 2023
Functional characterization and identification of a therapeutic for a novel SCN5A-F1760C variant causing type 3 long QT syndrome refractory to all guideline-directed therapiesMarissa J Stutzman, Xiaozhi Gao, Maengjo Kim, et al.Journal of Cardiovascular Electrophysiology|October 21, 2024
Frequency and Genotype-Dependence of intrinsic chronotropic insufficiency among patients with congenital long QT syndromeVeda K Kulkarni, Alexa M Pinsky, J Martijn Bos, et al.American Journal of Human Genetics|April 6, 2010
Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical recordMarylyn D Ritchie, Joshua C Denny, Dana C Crawford, et al.European Heart Journal|December 17, 2013
Surgical myectomy improves pulmonary hypertension in obstructive hypertrophic cardiomyopathyJeffrey B Geske, Tomas Konecny, Steve R Ommen, et al.IEEE Applied Imagery Pattern Recognition Workshop : [Proceedings]. IEEE Applied Imagery Pattern Recognition Workshop|June 2, 2018
The National Library of Medicine Pill Image Recognition Challenge: An Initial ReportZiv Yaniv, Jessica Faruque, Sally Howe, et al.Heart Rhythm|May 31, 2025
The clinical and electrocardiographic phenotype of patients with genotype-negative long QT syndromeVanessa Karlinski Vizentin, Raquel Neves, Sahej Bains, et al.JACC. Clinical Electrophysiology|February 7, 2025
Incidence and Clinical Management of Supraventricular Arrhythmias in Patients With Catecholaminergic Polymorphic Ventricular TachycardiaBrett C Austin, Gurukripa N Kowlgi, Raquel Almeida Lopes Neves, et al.European Heart Journal|August 10, 2005
Gene-specific modifying effects of pro-LVH polymorphisms involving the renin-angiotensin-aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathyMeghan J Perkins, Sara L Van Driest, Erik G Ellsworth, et al.Channels (Austin, Tex.)|July 10, 2018
Mexiletine rescues a mixed biophysical phenotype of the cardiac sodium channel arising from the SCN5A mutation, N406K, found in LQT3 patientsRou-Mu Hu, David J Tester, Ryan Li, et al.Journal of the American College of Cardiology|November 3, 2004
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathySara L Van Driest, Vlad C Vasile, Steve R Ommen, et al.Pageof 73