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Johan M Bos

Showing results (1-10 of 7) with videos related to

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International Journal of Cardiology|September 17, 2018
Prevalence and clinical phenotype of concomitant long QT syndrome and arrhythmogenic bileaflet mitral valve prolapseJohn R Giudicessi, Ram K Rohatgi, Johan M Bos, et al.
Studies in Health Technology and Informatics|January 25, 2024
Decision Support System Detecting Patients at Risk of Prolonged QT and Associated MortalityPedro J Caraballo, Johan M Bos, Ray Qian, et al.
Acta Cardiologica|March 8, 2018
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathySalma I Patel, Michael J Ackerman, Fadi E Shamoun, et al.
Human Molecular Genetics|January 31, 2012
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutationsEnkhsaikhan Purevjav, Takuro Arimura, Sibylle Augustin, et al.
Circulation|December 7, 2021
An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular TachycardiaPuck J Peltenburg, Dania Kallas, Johan M Bos, et al.
Circulation|July 25, 2024
Vigorous Exercise in Patients With Congenital Long QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS StudyRachel Lampert, Sharlene Day, Barbara Ainsworth, et al.
European Heart Journal|July 31, 2018
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroupsAlban-Elouen Baruteau, Florence Kyndt, Elijah R Behr, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
International Journal of Cardiology|September 17, 2018
Prevalence and clinical phenotype of concomitant long QT syndrome and arrhythmogenic bileaflet mitral valve prolapseJohn R Giudicessi, Ram K Rohatgi, Johan M Bos, et al.
Studies in Health Technology and Informatics|January 25, 2024
Decision Support System Detecting Patients at Risk of Prolonged QT and Associated MortalityPedro J Caraballo, Johan M Bos, Ray Qian, et al.
Acta Cardiologica|March 8, 2018
QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathySalma I Patel, Michael J Ackerman, Fadi E Shamoun, et al.
Human Molecular Genetics|January 31, 2012
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutationsEnkhsaikhan Purevjav, Takuro Arimura, Sibylle Augustin, et al.
Circulation|December 7, 2021
An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular TachycardiaPuck J Peltenburg, Dania Kallas, Johan M Bos, et al.
Circulation|July 25, 2024
Vigorous Exercise in Patients With Congenital Long QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS StudyRachel Lampert, Sharlene Day, Barbara Ainsworth, et al.
European Heart Journal|July 31, 2018
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroupsAlban-Elouen Baruteau, Florence Kyndt, Elijah R Behr, et al.
Pageof 1