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American Journal of Physiology. Heart and Circulatory Physiology|March 21, 2020
Abnormal myocardial expression of SAP97 is associated with arrhythmogenic riskHassan Musa, Cherisse A Marcou, Todd J Herron, et al.Lancet (London, England)|April 2, 2018
Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control studyRoope Männikkö, Leonie Wong, David J Tester, et al.Circulation|March 30, 2012
Mutations in cytoplasmic loops of the KCNQ1 channel and the risk of life-threatening events: implications for mutation-specific response to β-blocker therapy in type 1 long-QT syndromeAlon Barsheshet, Ilan Goldenberg, Jin O-Uchi, et al.Mayo Clinic Proceedings. Digital Health|April 10, 2025
Echocardiographic Diagnosis of Hypertrophic Cardiomyopathy by Machine LearningNasibeh Zanjirani Farahani, Mateo Alzate Aguirre, Vanessa Karlinski Vizentin, et al.British Journal of Sports Medicine|January 11, 2013
Abnormal electrocardiographic findings in athletes: recognising changes suggestive of primary electrical diseaseJonathan A Drezner, Michael J Ackerman, Bryan C Cannon, et al.Circulation|March 26, 2017
Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter RegistryKenichiro Yamagata, Minoru Horie, Takeshi Aiba, et al.Journal of the American College of Cardiology|December 28, 2010
Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervalsIlan Goldenberg, Samuel Horr, Arthur J Moss, et al.Circulation|May 29, 2015
Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic DenervationGaetano M De Ferrari, Veronica Dusi, Carla Spazzolini, et al.British Journal of Sports Medicine|January 11, 2013
Abnormal electrocardiographic findings in athletes: recognising changes suggestive of cardiomyopathyJonathan A Drezner, Euan Ashley, Aaron L Baggish, et al.Circulation|November 14, 2007
Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel functionStephan E Lehnart, Michael J Ackerman, D Woodrow Benson, et al.Pageof 73