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The Journal of Pediatrics|October 1, 2018
Exome-Wide Rare Variant Analyses in Sudden Infant Death SyndromeDavid J Tester, Leonie C H Wong, Pritha Chanana, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2018
Noncardiac genetic predisposition in sudden infant death syndromeBelinda Gray, David J Tester, Leonie Ch Wong, et al.
Brain : a Journal of Neurology|December 17, 2021
Andersen-Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidityVinojini Vivekanandam, Roope Männikkö, Iwona Skorupinska, et al.
Journal of the American College of Cardiology|October 8, 2021
Biventricular Myocardial Fibrosis and Sudden Death in Patients With Brugada SyndromeChris Miles, Angeliki Asimaki, Irina Chis Ster, et al.
Genome Medicine|December 28, 2022
The role of genetic testing in diagnosis and care of inherited cardiac conditions in a specialised multidisciplinary clinicFergus Stafford, Neesha Krishnan, Ebony Richardson, et al.
Heart, Lung & Circulation|July 7, 2023
The New South Wales Sudden Cardiac Arrest Registry: A Data Linkage Cohort StudyFelicity Leslie, Suzanne R Avis, Richard D Bagnall, 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|February 4, 2020
Diagnostic yield of hypertrophic cardiomyopathy in first-degree relatives of decedents with idiopathic left ventricular hypertrophyGherardo Finocchiaro, Harshil Dhutia, Belinda Gray, et al.
Journal of the American College of Cardiology|March 17, 2018
The Diagnostic Yield of Brugada Syndrome After Sudden Death With Normal AutopsyMichael Papadakis, Efstathios Papatheodorou, Greg Mellor, et al.
European Journal of Preventive Cardiology|September 7, 2022
Indications and utility of cardiac genetic testing in athletesSilvia Castelletti, Belinda Gray, Cristina Basso, et al.
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