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Circulation. Cardiovascular Genetics|September 13, 2014
Evaluation of genes encoding for the transient outward current (Ito) identifies the KCND2 gene as a cause of J-wave syndrome associated with sudden cardiac deathMark J Perrin, Arnon Adler, Sharon Green, et al.JACC. Advances|June 17, 2026
Clinical Spectrum and Outcomes in Hypertrophic Cardiomyopathy With Apical Aneurysms: A Large Multicenter International CohortEthan J Rowin, Deacon Z J Lee, Mark V Sherrid, et al.Orphanet Journal of Rare Diseases|August 11, 2021
The GoodHope Ehlers Danlos Syndrome Clinic: development and implementation of the first interdisciplinary program for multi-system issues in connective tissue disorders at the Toronto General HospitalNimish Mittal, Daniel Santa Mina, Laura McGillis, et al.Circulation. Arrhythmia and Electrophysiology|July 9, 2021
Management of Congenital Long-QT Syndrome: Commentary From the ExpertsElizabeth S Kaufman, Lee L Eckhardt, Michael J Ackerman, et al.The American Journal of Cardiology|August 14, 2022
Ventricular Septal Myectomy for Obstructive Hypertrophic Cardiomyopathy (Analysis Spanning 60 Years Of Practice): AJC Expert PanelBarry J Maron, Joseph A Dearani, Nicholas G Smedira, et al.Journal of Arrhythmia|October 21, 2016
Erratum to '2015 HRS/EHRA/APHRS/SOLAECE expert consensus statement on optimal implantable cardioverter-defibrillator programming and testing' [Journal of Arrhythmia 32/1 (2016) 1-28]Bruce L Wilkoff, Laurent Fauchier, Martin K Stiles, et al.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.Journal of Medical Genetics|June 26, 2020
Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort studySalma Shickh, Mariana Gutierrez Salazar, Kathleen-Rose Zakoor, et al.Genome Medicine|October 23, 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.Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathyRafik Tadros, Sean L Zheng, Christopher Grace, et al.Pageof 16