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Seiko Ohno

Showing results (181-190 of 196) with videos related to

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Circulation Journal : Official Journal of the Japanese Circulation Society|October 7, 2021
Electrocardiographic Diagnosis of Hypertrophic Cardiomyopathy in the Pre- and Post-Diagnostic Phases in Children and AdolescentsMasao Yoshinaga, Hitoshi Horigome, Mamoru Ayusawa, 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|May 11, 2026
Ventricular conduction is a marker for arrhythmic risk in SCN5A-E1784K overlap sodium channel diseaseMichael W T Tanck, Yanushi D Wijeyeratne, Julien Barc, et al.
European Heart Journal|May 31, 2019
Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrestChristian 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 StratificationMatthew J O'Neill, Chai-Ann Ng, Takanori Aizawa, 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 StratificationMatthew 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 defectsManon Baudic, Hiroshige Murata, Fernanda M Bosada, et al.
European Heart Journal|June 7, 2019
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, David J Tester, 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> FamiliesYanushi 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 tachycardiaAvani Lamba, Thomas M Roston, Puck J Peltenburg, et al.
European Heart Journal|August 2, 2023
Clinical presentation of calmodulin mutations: the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, Mette Nyegaard, et al.
Pageof 20

Showing results (181-190 of 196) with videos related to

Sort By:
Pageof 20
Circulation Journal : Official Journal of the Japanese Circulation Society|October 7, 2021
Electrocardiographic Diagnosis of Hypertrophic Cardiomyopathy in the Pre- and Post-Diagnostic Phases in Children and AdolescentsMasao Yoshinaga, Hitoshi Horigome, Mamoru Ayusawa, 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|May 11, 2026
Ventricular conduction is a marker for arrhythmic risk in SCN5A-E1784K overlap sodium channel diseaseMichael W T Tanck, Yanushi D Wijeyeratne, Julien Barc, et al.
European Heart Journal|May 31, 2019
Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrestChristian 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 StratificationMatthew J O'Neill, Chai-Ann Ng, Takanori Aizawa, 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 StratificationMatthew 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 defectsManon Baudic, Hiroshige Murata, Fernanda M Bosada, et al.
European Heart Journal|June 7, 2019
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, David J Tester, 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> FamiliesYanushi 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 tachycardiaAvani Lamba, Thomas M Roston, Puck J Peltenburg, et al.
European Heart Journal|August 2, 2023
Clinical presentation of calmodulin mutations: the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, Mette Nyegaard, et al.
Pageof 20