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Johan Saenen

Showing results (21-30 of 52) with videos related to

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Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|October 2, 2023
Atrial fibrillation cycle-length (AF-CL) inside the pulmonary veins predicts paroxysmal AF ablation success- the INDUCE-AF studyMarco Bergonti, Ciro Ascione, Paolo Compagnucci, et al.
The American Journal of Cardiology|January 17, 2021
Effect of Mitral Regurgitation on Thrombotic Risk in Patients With Nonrheumatic Atrial Fibrillation: A New CHA<sub>2</sub>DS<sub>2</sub>-VASc Score Risk Modifier?Sven L Van Laer, Seppe Verreyen, Koen M Winkler, et al.
The Journal of Molecular Diagnostics : JMD|March 26, 2017
Targeted Next-Generation Sequencing of 51 Genes Involved in Primary Electrical DiseaseDorien Proost, Johan Saenen, Geert Vandeweyer, et al.
Heart Rhythm|September 24, 2013
Life-threatening ventricular arrhythmias during ajmaline challenge in patients with Brugada syndrome: incidence, clinical features, and prognosisGiulio Conte, Juan Sieira, Andrea Sarkozy, et al.
Frontiers in Genetics|September 18, 2023
Variable clinical expression of a Belgian <i>TGFB3</i> founder variant suggests the presence of a genetic modifierMelanie H A M Perik, Emmanuela Govaerts, Steven Laga, et al.
Heart Rhythm|January 14, 2023
Anterior mitral line in patients with persistent atrial fibrillation and anterior scar: A multicenter matched comparison-The MiLine studyMarco Bergonti, Francesco Raffaele Spera, Teba Gonzalez Ferrero, et al.
Journal of Cardiovascular Electrophysiology|April 23, 2023
Microelectrode voltage mapping for substrate assessment in catheter ablation of ventricular tachycardia: A dual-center experienceAntonio Dello Russo, Paolo Compagnucci, Marco Bergonti, et al.
Frontiers in Cardiovascular Medicine|August 28, 2020
Compound Heterozygous <i>SCN5A</i> Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case ReportAleksandra Nijak, Alain J Labro, Hans De Wilde, et al.
Orphanet Journal of Rare Diseases|February 1, 2023
Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian populationEwa Sieliwonczyk, Maaike Alaerts, Eline Simons, et al.
Human Mutation|April 25, 2015
Performant Mutation Identification Using Targeted Next-Generation Sequencing of 14 Thoracic Aortic Aneurysm GenesDorien Proost, Geert Vandeweyer, Josephina A N Meester, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

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Pageof 6
Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|October 2, 2023
Atrial fibrillation cycle-length (AF-CL) inside the pulmonary veins predicts paroxysmal AF ablation success- the INDUCE-AF studyMarco Bergonti, Ciro Ascione, Paolo Compagnucci, et al.
The American Journal of Cardiology|January 17, 2021
Effect of Mitral Regurgitation on Thrombotic Risk in Patients With Nonrheumatic Atrial Fibrillation: A New CHA<sub>2</sub>DS<sub>2</sub>-VASc Score Risk Modifier?Sven L Van Laer, Seppe Verreyen, Koen M Winkler, et al.
The Journal of Molecular Diagnostics : JMD|March 26, 2017
Targeted Next-Generation Sequencing of 51 Genes Involved in Primary Electrical DiseaseDorien Proost, Johan Saenen, Geert Vandeweyer, et al.
Heart Rhythm|September 24, 2013
Life-threatening ventricular arrhythmias during ajmaline challenge in patients with Brugada syndrome: incidence, clinical features, and prognosisGiulio Conte, Juan Sieira, Andrea Sarkozy, et al.
Frontiers in Genetics|September 18, 2023
Variable clinical expression of a Belgian <i>TGFB3</i> founder variant suggests the presence of a genetic modifierMelanie H A M Perik, Emmanuela Govaerts, Steven Laga, et al.
Heart Rhythm|January 14, 2023
Anterior mitral line in patients with persistent atrial fibrillation and anterior scar: A multicenter matched comparison-The MiLine studyMarco Bergonti, Francesco Raffaele Spera, Teba Gonzalez Ferrero, et al.
Journal of Cardiovascular Electrophysiology|April 23, 2023
Microelectrode voltage mapping for substrate assessment in catheter ablation of ventricular tachycardia: A dual-center experienceAntonio Dello Russo, Paolo Compagnucci, Marco Bergonti, et al.
Frontiers in Cardiovascular Medicine|August 28, 2020
Compound Heterozygous <i>SCN5A</i> Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case ReportAleksandra Nijak, Alain J Labro, Hans De Wilde, et al.
Orphanet Journal of Rare Diseases|February 1, 2023
Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian populationEwa Sieliwonczyk, Maaike Alaerts, Eline Simons, et al.
Human Mutation|April 25, 2015
Performant Mutation Identification Using Targeted Next-Generation Sequencing of 14 Thoracic Aortic Aneurysm GenesDorien Proost, Geert Vandeweyer, Josephina A N Meester, et al.
Pageof 6