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Eric Schulze

Showing results (141-150 of 155) with videos related to

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Circulation. Arrhythmia and Electrophysiology|July 9, 2021
Management of Congenital Long-QT Syndrome: Commentary From the ExpertsElizabeth S Kaufman, Lee L Eckhardt, Michael J Ackerman, 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|April 1, 2025
The diagnostic role of pharmacological provocation testing in cardiac electrophysiology: a clinical consensus statement of the European Heart Rhythm Association and the European Association of Percutaneous Cardiovascular Interventions (EAPCI) of the ESC, the ESC Working Group on Cardiovascular Pharmacotherapy, the Association of European Paediatric and Congenital Cardiology (AEPC), the Paediatric & Congenital Electrophysiology Society (PACES), the Heart Rhythm Society (HRS), the Asia Pacific Heart Rhythm Society (APHRS), and the Latin American Heart Rhythm Society (LAHRS)Elijah R Behr, Bo Gregers Winkel, Bode Ensam, et al.
European Heart Journal|July 2, 2025
Long QT syndrome in children and adolescents: risk factors and outcomes in a large German cohortLea Lippert, Tobias Burkard, Franziska Markel, et al.
Plos One|November 14, 2013
Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizesElijah R Behr, Marylyn D Ritchie, Toshihiro Tanaka, et al.
Journal of the American Society of Nephrology : JASN|October 5, 2021
mTOR-Activating Mutations in <i>RRAGD</i> Are Causative for Kidney Tubulopathy and CardiomyopathyKarl P Schlingmann, François Jouret, Kuang Shen, et al.
Circulation. Cardiovascular Genetics|November 22, 2011
A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointesStefan Kääb, Dana C Crawford, Moritz F Sinner, et al.
JACC. Clinical Electrophysiology|April 14, 2026
Clinical Profile and Mode of Initiation of Spontaneous Ventricular Tachyarrhythmias in Patients With Brugada Syndrome (START-BrS)Anat Milman, Koonlawee Nademanee, Tsukasa Kamakura, et al.
JACC. Clinical Electrophysiology|June 6, 2024
Mode and Characteristics of Arrhythmia Initiation in Idiopathic Ventricular Fibrillation: A THESIS SubstudyBernard Belhassen, Giulio Conte, Christian Steinberg, et al.
European Heart Journal|September 17, 2024
Clinical features and outcomes in carriers of pathogenic desmoplakin variantsAlessio Gasperetti, Richard T Carrick, Alexandros Protonotarios, 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 deathConnie R Bezzina, Julien Barc, Yuka Mizusawa, et al.
Pageof 16

Showing results (141-150 of 155) with videos related to

Sort By:
Pageof 16
Circulation. Arrhythmia and Electrophysiology|July 9, 2021
Management of Congenital Long-QT Syndrome: Commentary From the ExpertsElizabeth S Kaufman, Lee L Eckhardt, Michael J Ackerman, 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|April 1, 2025
The diagnostic role of pharmacological provocation testing in cardiac electrophysiology: a clinical consensus statement of the European Heart Rhythm Association and the European Association of Percutaneous Cardiovascular Interventions (EAPCI) of the ESC, the ESC Working Group on Cardiovascular Pharmacotherapy, the Association of European Paediatric and Congenital Cardiology (AEPC), the Paediatric & Congenital Electrophysiology Society (PACES), the Heart Rhythm Society (HRS), the Asia Pacific Heart Rhythm Society (APHRS), and the Latin American Heart Rhythm Society (LAHRS)Elijah R Behr, Bo Gregers Winkel, Bode Ensam, et al.
European Heart Journal|July 2, 2025
Long QT syndrome in children and adolescents: risk factors and outcomes in a large German cohortLea Lippert, Tobias Burkard, Franziska Markel, et al.
Plos One|November 14, 2013
Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizesElijah R Behr, Marylyn D Ritchie, Toshihiro Tanaka, et al.
Journal of the American Society of Nephrology : JASN|October 5, 2021
mTOR-Activating Mutations in <i>RRAGD</i> Are Causative for Kidney Tubulopathy and CardiomyopathyKarl P Schlingmann, François Jouret, Kuang Shen, et al.
Circulation. Cardiovascular Genetics|November 22, 2011
A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointesStefan Kääb, Dana C Crawford, Moritz F Sinner, et al.
JACC. Clinical Electrophysiology|April 14, 2026
Clinical Profile and Mode of Initiation of Spontaneous Ventricular Tachyarrhythmias in Patients With Brugada Syndrome (START-BrS)Anat Milman, Koonlawee Nademanee, Tsukasa Kamakura, et al.
JACC. Clinical Electrophysiology|June 6, 2024
Mode and Characteristics of Arrhythmia Initiation in Idiopathic Ventricular Fibrillation: A THESIS SubstudyBernard Belhassen, Giulio Conte, Christian Steinberg, et al.
European Heart Journal|September 17, 2024
Clinical features and outcomes in carriers of pathogenic desmoplakin variantsAlessio Gasperetti, Richard T Carrick, Alexandros Protonotarios, 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 deathConnie R Bezzina, Julien Barc, Yuka Mizusawa, et al.
Pageof 16