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Medrxiv : the Preprint Server for Health Sciences|April 17, 2023
Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditionsKatherine S Josephs, Angharad M Roberts, Pantazis Theotokis, et al.
Circulation. Arrhythmia and Electrophysiology|August 11, 2017
Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?Jason D Roberts, Andrew D Krahn, Michael J Ackerman, et al.
Heart Rhythm|September 1, 2018
Linking the heart and the brain: Neurodevelopmental disorders in patients with catecholaminergic polymorphic ventricular tachycardiaKrystien V V Lieve, Judith M A Verhagen, Jinhong Wei, et al.
Circulation. Arrhythmia and Electrophysiology|February 18, 2020
Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular TachycardiaKrystien V V Lieve, Veronica Dusi, Christian van der Werf, et al.
Circulation. Arrhythmia and Electrophysiology|January 29, 2026
Left Ventricular Late Gadolinium Enhancement for Arrhythmic Risk Prediction in ARVCCorrado De Marco, Babken Asatryan, Anneline S J M Te Riele, et al.
JAMA Cardiology|April 8, 2026
RBM20 Truncating Variants and Human CardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
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