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JACC. Clinical Electrophysiology|June 28, 2023
Ventricular Tachycardia and ICD Therapy Burden With Catheter Ablation Versus Escalated Antiarrhythmic Drug TherapyMichelle Samuel, Jeff S Healey, Isabelle Nault, et al.BMC Cardiovascular Disorders|October 22, 2020
The effect of revascularization on mortality and risk of ventricular arrhythmia in patients with ischemic cardiomyopathyAhmad Alkharaza, Mousa Al-Harbi, Ihab El-Sokkari, et al.Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|January 14, 2022
Ventricular tachycardia characteristics and outcomes with catheter ablation vs. antiarrhythmic therapy: insights from the VANISH trialMarc W Deyell, Steve Doucette, Ratika Parkash, et al.Journal of Cardiovascular Electrophysiology|March 5, 2011
Does adenosine response predict clinical recurrence of atrial fibrillation after pulmonary vein isolation?Lorne J Gula, David Massel, Peter Leong-Sit, et al.American Journal of Medical Genetics. Part A|July 15, 2024
Expanding the clinical phenotype and variant spectrum associated with RFX7Talia Sisroe, Attila Dos Santos, Alyssa L Rippert, et al.Journal of Cardiovascular Electrophysiology|October 13, 2009
Expression of a common LQT1 mutation in five apparently unrelated families in a regional inherited arrhythmia clinicChristopher Gray, Lorne J Gula, George J Klein, et al.American Journal of Medical Genetics. Part A|May 2, 2022
MYH7 variants cause complex congenital heart diseaseAlyssa Ritter, Jacqueline Leonard, Christopher Gray, et al.The British Journal of Dermatology|May 25, 2026
Loss-of-function variants in EPHX3 cause nonsyndromic epidermal differentiation disordersKunlun Lv, Karina M Forde, Amanda T Moon, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2019
Clinical utility of exome sequencing in infantile heart failureAlyssa Ritter, Emma Bedoukian, Justin H Berger, et al.American Journal of Medical Genetics. Part A|May 22, 2023
Retrospective identification of patients with SRRM2-related neurodevelopmental disorder in a single tertiary children's hospitalKelly E Regan-Fendt, Alyssa L Rippert, Livija Medne, et al.Pageof 5