Search research articles
Contact Us
Filters
Showing results (411-420 of 428) with videos related to
Page
of 43
Sort By:
Heart Rhythm
|
May 2, 2022
2022 HRS expert consensus statement on evaluation and management of arrhythmic risk in neuromuscular disorders
William J Groh, Deepak Bhakta, Gordon F Tomaselli, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 19, 2024
Multiplexed Assays of Variant Effect and Automated Patch-clamping Improve <i>KCNH2</i>-LQTS Variant Classification and Cardiac Event Risk Stratification
Matthew J O'Neill, Chai-Ann Ng, Takanori Aizawa, et al.
Nature Communications
|
April 20, 2024
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects
Manon Baudic, Hiroshige Murata, Fernanda M Bosada, et al.
European Heart Journal
|
May 31, 2019
Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest
Christian van der Werf, Krystien V Lieve, J Martijn Bos, et al.
Circulation
|
September 24, 2024
Multiplexed Assays of Variant Effect and Automated Patch Clamping Improve <i>KCNH2</i>-LQTS Variant Classification and Cardiac Event Risk Stratification
Matthew J O'Neill, Chai-Ann Ng, Takanori Aizawa, et al.
Journal of the American Heart Association
|
June 17, 2015
Clinical efficacy of thrombus aspiration on 5-year clinical outcomes in patients with ST-segment elevation acute myocardial infarction undergoing percutaneous coronary intervention
Hiroki Watanabe, Hiroki Shiomi, Kenji Nakatsuma, et al.
European Heart Journal
|
June 7, 2019
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry
Lia Crotti, Carla Spazzolini, David J Tester, et al.
Journal of Cardiovascular Translational Research
|
July 7, 2023
A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients
Emilia Nagyova, Edgar T Hoorntje, Wouter P Te Rijdt, et al.
Circulation. Genomic and Precision Medicine
|
November 9, 2020
<i>SCN5A</i> Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in <i>SCN5A</i> Families
Yanushi D Wijeyeratne, Michael W Tanck, Yuka Mizusawa, et al.
Heart Rhythm
|
April 8, 2024
An international multicenter cohort study on implantable cardioverter-defibrillators for the treatment of symptomatic children with catecholaminergic polymorphic ventricular tachycardia
Avani Lamba, Thomas M Roston, Puck J Peltenburg, et al.
Page
of 43
Search research articles
Search
Showing results (411-420 of 428) with videos related to
Sort By:
Page
of 43
Heart Rhythm
|
May 2, 2022
2022 HRS expert consensus statement on evaluation and management of arrhythmic risk in neuromuscular disorders
William J Groh, Deepak Bhakta, Gordon F Tomaselli, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 19, 2024
Multiplexed Assays of Variant Effect and Automated Patch-clamping Improve <i>KCNH2</i>-LQTS Variant Classification and Cardiac Event Risk Stratification
Matthew J O'Neill, Chai-Ann Ng, Takanori Aizawa, et al.
Nature Communications
|
April 20, 2024
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects
Manon Baudic, Hiroshige Murata, Fernanda M Bosada, et al.
European Heart Journal
|
May 31, 2019
Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest
Christian van der Werf, Krystien V Lieve, J Martijn Bos, et al.
Circulation
|
September 24, 2024
Multiplexed Assays of Variant Effect and Automated Patch Clamping Improve <i>KCNH2</i>-LQTS Variant Classification and Cardiac Event Risk Stratification
Matthew J O'Neill, Chai-Ann Ng, Takanori Aizawa, et al.
Journal of the American Heart Association
|
June 17, 2015
Clinical efficacy of thrombus aspiration on 5-year clinical outcomes in patients with ST-segment elevation acute myocardial infarction undergoing percutaneous coronary intervention
Hiroki Watanabe, Hiroki Shiomi, Kenji Nakatsuma, et al.
European Heart Journal
|
June 7, 2019
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry
Lia Crotti, Carla Spazzolini, David J Tester, et al.
Journal of Cardiovascular Translational Research
|
July 7, 2023
A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients
Emilia Nagyova, Edgar T Hoorntje, Wouter P Te Rijdt, et al.
Circulation. Genomic and Precision Medicine
|
November 9, 2020
<i>SCN5A</i> Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in <i>SCN5A</i> Families
Yanushi D Wijeyeratne, Michael W Tanck, Yuka Mizusawa, et al.
Heart Rhythm
|
April 8, 2024
An international multicenter cohort study on implantable cardioverter-defibrillators for the treatment of symptomatic children with catecholaminergic polymorphic ventricular tachycardia
Avani Lamba, Thomas M Roston, Puck J Peltenburg, et al.
Page
of 43