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Circulation
|
December 7, 2021
An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia
Puck J Peltenburg, Dania Kallas, Johan M Bos, et al.
Circulation
|
October 27, 2023
Flecainide Is Associated With a Lower Incidence of Arrhythmic Events in a Large Cohort of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
Auke T Bergeman, Krystien V V Lieve, Dania Kallas, et al.
Nature Genetics
|
July 23, 2013
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
Connie R Bezzina, Julien Barc, Yuka Mizusawa, et al.
European Heart Journal
|
December 19, 2025
Catecholaminergic polymorphic ventricular tachycardia mediated by ryanodine receptor 2: a validated risk stratification
Krystien V Lieve, Christian van der Werf, Dania Kallas, et al.
Circulation
|
May 21, 2020
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
Najim Lahrouchi, Rafik Tadros, Lia Crotti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
Roddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.
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Showing results (191-200 of 196) with videos related to
Sort By:
Page
of 20
You have reached the last page of results.
This site can display upto 196 results.
Circulation
|
December 7, 2021
An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia
Puck J Peltenburg, Dania Kallas, Johan M Bos, et al.
Circulation
|
October 27, 2023
Flecainide Is Associated With a Lower Incidence of Arrhythmic Events in a Large Cohort of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
Auke T Bergeman, Krystien V V Lieve, Dania Kallas, et al.
Nature Genetics
|
July 23, 2013
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
Connie R Bezzina, Julien Barc, Yuka Mizusawa, et al.
European Heart Journal
|
December 19, 2025
Catecholaminergic polymorphic ventricular tachycardia mediated by ryanodine receptor 2: a validated risk stratification
Krystien V Lieve, Christian van der Werf, Dania Kallas, et al.
Circulation
|
May 21, 2020
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
Najim Lahrouchi, Rafik Tadros, Lia Crotti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
Roddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.
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of 20