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J Martijn Bos

Showing results (71-80 of 170) with videos related to

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Pediatric Cardiology|April 8, 2015
Phenotype of Children with QT Prolongation Identified Using an Institution-Wide QT Alert SystemHeather N Anderson, J Martijn Bos, Kristina H Haugaa, et al.
The American Journal of Cardiology|September 28, 2015
Frequency and cause of transient QT prolongation after surgeryDaniel D Joyce, J Martijn Bos, Kristina H Haugaa, 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|March 5, 2026
Calcium release channel deficiency syndrome in patients diagnosed with idiopathic ventricular fibrillation and decedents classified as sudden unexplained death in the youngLucilla Giammarino, Raquel Neves, David J Tester, et al.
Heart Rhythm|April 19, 2017
Cardiac transplantation in children and adolescents with long QT syndromeAngela M Kelle, J Martijn Bos, Susan P Etheridge, et al.
The American Journal of Cardiology|February 24, 2020
Cardiac Magnetic Resonance Imaging Features in Hypertrophic Cardiomyopathy Diagnosed at <21 Years of AgeErica D Bonura, J Martijn Bos, Mahmoud A Abdelsalam, et al.
Journal of Cardiovascular Electrophysiology|October 21, 2024
Frequency and Genotype-Dependence of intrinsic chronotropic insufficiency among patients with congenital long QT syndromeVeda K Kulkarni, Alexa M Pinsky, J Martijn Bos, et al.
JACC. Clinical Electrophysiology|February 7, 2025
Incidence and Clinical Management of Supraventricular Arrhythmias in Patients With Catecholaminergic Polymorphic Ventricular TachycardiaBrett C Austin, Gurukripa N Kowlgi, Raquel Almeida Lopes Neves, et al.
Heart Rhythm|May 31, 2025
The clinical and electrocardiographic phenotype of patients with genotype-negative long QT syndromeVanessa Karlinski Vizentin, Raquel Neves, Sahej Bains, et al.
Circulation. Genomic and Precision Medicine|September 7, 2020
Clinical Utility of a Phenotype-Enhanced <i>MYH7</i>-Specific Variant Classification Framework in Hypertrophic Cardiomyopathy Genetic TestingConnor L Mattivi, J Martijn Bos, Richard D Bagnall, et al.
The American Journal of Cardiology|November 10, 2010
Role of family history of sudden death in risk stratification and prevention of sudden death with implantable defibrillators in hypertrophic cardiomyopathyJ Martijn Bos, Barry J Maron, Michael J Ackerman, et al.
Pageof 17

Showing results (71-80 of 170) with videos related to

Sort By:
Pageof 17
Pediatric Cardiology|April 8, 2015
Phenotype of Children with QT Prolongation Identified Using an Institution-Wide QT Alert SystemHeather N Anderson, J Martijn Bos, Kristina H Haugaa, et al.
The American Journal of Cardiology|September 28, 2015
Frequency and cause of transient QT prolongation after surgeryDaniel D Joyce, J Martijn Bos, Kristina H Haugaa, 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|March 5, 2026
Calcium release channel deficiency syndrome in patients diagnosed with idiopathic ventricular fibrillation and decedents classified as sudden unexplained death in the youngLucilla Giammarino, Raquel Neves, David J Tester, et al.
Heart Rhythm|April 19, 2017
Cardiac transplantation in children and adolescents with long QT syndromeAngela M Kelle, J Martijn Bos, Susan P Etheridge, et al.
The American Journal of Cardiology|February 24, 2020
Cardiac Magnetic Resonance Imaging Features in Hypertrophic Cardiomyopathy Diagnosed at <21 Years of AgeErica D Bonura, J Martijn Bos, Mahmoud A Abdelsalam, et al.
Journal of Cardiovascular Electrophysiology|October 21, 2024
Frequency and Genotype-Dependence of intrinsic chronotropic insufficiency among patients with congenital long QT syndromeVeda K Kulkarni, Alexa M Pinsky, J Martijn Bos, et al.
JACC. Clinical Electrophysiology|February 7, 2025
Incidence and Clinical Management of Supraventricular Arrhythmias in Patients With Catecholaminergic Polymorphic Ventricular TachycardiaBrett C Austin, Gurukripa N Kowlgi, Raquel Almeida Lopes Neves, et al.
Heart Rhythm|May 31, 2025
The clinical and electrocardiographic phenotype of patients with genotype-negative long QT syndromeVanessa Karlinski Vizentin, Raquel Neves, Sahej Bains, et al.
Circulation. Genomic and Precision Medicine|September 7, 2020
Clinical Utility of a Phenotype-Enhanced <i>MYH7</i>-Specific Variant Classification Framework in Hypertrophic Cardiomyopathy Genetic TestingConnor L Mattivi, J Martijn Bos, Richard D Bagnall, et al.
The American Journal of Cardiology|November 10, 2010
Role of family history of sudden death in risk stratification and prevention of sudden death with implantable defibrillators in hypertrophic cardiomyopathyJ Martijn Bos, Barry J Maron, Michael J Ackerman, et al.
Pageof 17