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Isabelle Denjoy

Showing results (51-60 of 116) with videos related to

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Cardiovascular Research|June 15, 2004
New KCNQ1 mutations leading to haploinsufficiency in a general population; Defective trafficking of a KvLQT1 mutantLaetitia Gouas, Chloe Bellocq, Myriam Berthet, et al.
Heart Rhythm O2|November 24, 2025
Clinical presentation and outcomes of patients with biallelic <i>SCN5A</i> variants: A systematic reviewElodie Surget, Alexis Hermida, Alice Maltret, et al.
Human Mutation|September 3, 2011
Mutational spectrum in the Ca(2+)--activated cation channel gene TRPM4 in patients with cardiac conductance disturbancesBirgit Stallmeyer, Sven Zumhagen, Isabelle Denjoy, et al.
Circulation Research|October 19, 2002
Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardiaAlex V Postma, Isabelle Denjoy, Theo M Hoorntje, 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 11, 2026
Clinical profile and prognosis of brugada syndrome SCN5A variant carriers with negative sodium channel blocker challengeElodie Surget, Gael Clerici, Frédéric Sacher, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|June 30, 2015
A Common Mutation of Long QT Syndrome Type 1 in JapanHideki Itoh, Kenichi Dochi, Wataru Shimizu, et al.
CJC Open|March 29, 2021
Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation StateQuentin Plumereau, Olivier Theriault, Valérie Pouliot, et al.
Archives of Cardiovascular Diseases|May 4, 2024
Wearable electrocardiogram devices in patients with congenital long QT syndrome: The SMART-QT studyAntoine Delinière, Francis Bessière, Leslie Placide, et al.
Archives of Cardiovascular Diseases|November 8, 2024
Automatized quantitative electrocardiography from digitized paper electrocardiograms: A new avenue for risk stratification in patients with Brugada syndromePierre-Léo Laporte, Martino Vaglio, Isabelle Denjoy, et al.
Circulation|February 8, 2006
The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcomePeter J Schwartz, Carla Spazzolini, Lia Crotti, et al.
Pageof 12

Showing results (51-60 of 116) with videos related to

Sort By:
Pageof 12
Cardiovascular Research|June 15, 2004
New KCNQ1 mutations leading to haploinsufficiency in a general population; Defective trafficking of a KvLQT1 mutantLaetitia Gouas, Chloe Bellocq, Myriam Berthet, et al.
Heart Rhythm O2|November 24, 2025
Clinical presentation and outcomes of patients with biallelic <i>SCN5A</i> variants: A systematic reviewElodie Surget, Alexis Hermida, Alice Maltret, et al.
Human Mutation|September 3, 2011
Mutational spectrum in the Ca(2+)--activated cation channel gene TRPM4 in patients with cardiac conductance disturbancesBirgit Stallmeyer, Sven Zumhagen, Isabelle Denjoy, et al.
Circulation Research|October 19, 2002
Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardiaAlex V Postma, Isabelle Denjoy, Theo M Hoorntje, 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 11, 2026
Clinical profile and prognosis of brugada syndrome SCN5A variant carriers with negative sodium channel blocker challengeElodie Surget, Gael Clerici, Frédéric Sacher, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|June 30, 2015
A Common Mutation of Long QT Syndrome Type 1 in JapanHideki Itoh, Kenichi Dochi, Wataru Shimizu, et al.
CJC Open|March 29, 2021
Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation StateQuentin Plumereau, Olivier Theriault, Valérie Pouliot, et al.
Archives of Cardiovascular Diseases|May 4, 2024
Wearable electrocardiogram devices in patients with congenital long QT syndrome: The SMART-QT studyAntoine Delinière, Francis Bessière, Leslie Placide, et al.
Archives of Cardiovascular Diseases|November 8, 2024
Automatized quantitative electrocardiography from digitized paper electrocardiograms: A new avenue for risk stratification in patients with Brugada syndromePierre-Léo Laporte, Martino Vaglio, Isabelle Denjoy, et al.
Circulation|February 8, 2006
The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcomePeter J Schwartz, Carla Spazzolini, Lia Crotti, et al.
Pageof 12