Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A A Wilde

Showing results (61-70 of 78) with videos related to

Pageof 8
Sort By:
Nature Genetics|September 2, 1999
Cardiac conduction defects associate with mutations in SCN5AJ J Schott, C Alshinawi, F Kyndt, et al.
Journal of the American College of Cardiology|June 1, 1990
Ventricular tachycardia in the infarcted, Langendorff-perfused human heart: role of the arrangement of surviving cardiac fibersJ M de Bakker, R Coronel, S Tasseron, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|August 24, 2010
Dronedarone in patients with atrial fibrillationN M S de Groot, C J Kirchhof, I C van Gelder, et al.
Cardiovascular Research|February 26, 2000
Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndromeM B Rook, C Bezzina Alshinawi, W A Groenewegen, et al.
Human Genetics|September 1, 1997
The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 geneM H van den Berg, A A Wilde, E O Robles de Medina, et al.
Journal of the American College of Cardiology|November 6, 2001
Alterations in potassium channel gene expression in atria of patients with persistent and paroxysmal atrial fibrillation: differential regulation of protein and mRNA levels for K+ channelsB J Brundel, I C Van Gelder, R H Henning, et al.
Circulation|March 1, 1988
Reentry as a cause of ventricular tachycardia in patients with chronic ischemic heart disease: electrophysiologic and anatomic correlationJ M de Bakker, F J van Capelle, M J Janse, et al.
Journal of the American College of Cardiology|February 11, 1999
Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1)A A Wilde, R J Jongbloed, P A Doevendans, et al.
Nature|March 10, 2001
A sodium-channel mutation causes isolated cardiac conduction diseaseH L Tan, M T Bink-Boelkens, C R Bezzina, et al.
Circulation|September 6, 2001
De novo mutation in the SCN5A gene associated with early onset of sudden infant deathH Wedekind, J P Smits, E Schulze-Bahr, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Nature Genetics|September 2, 1999
Cardiac conduction defects associate with mutations in SCN5AJ J Schott, C Alshinawi, F Kyndt, et al.
Journal of the American College of Cardiology|June 1, 1990
Ventricular tachycardia in the infarcted, Langendorff-perfused human heart: role of the arrangement of surviving cardiac fibersJ M de Bakker, R Coronel, S Tasseron, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|August 24, 2010
Dronedarone in patients with atrial fibrillationN M S de Groot, C J Kirchhof, I C van Gelder, et al.
Cardiovascular Research|February 26, 2000
Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndromeM B Rook, C Bezzina Alshinawi, W A Groenewegen, et al.
Human Genetics|September 1, 1997
The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 geneM H van den Berg, A A Wilde, E O Robles de Medina, et al.
Journal of the American College of Cardiology|November 6, 2001
Alterations in potassium channel gene expression in atria of patients with persistent and paroxysmal atrial fibrillation: differential regulation of protein and mRNA levels for K+ channelsB J Brundel, I C Van Gelder, R H Henning, et al.
Circulation|March 1, 1988
Reentry as a cause of ventricular tachycardia in patients with chronic ischemic heart disease: electrophysiologic and anatomic correlationJ M de Bakker, F J van Capelle, M J Janse, et al.
Journal of the American College of Cardiology|February 11, 1999
Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1)A A Wilde, R J Jongbloed, P A Doevendans, et al.
Nature|March 10, 2001
A sodium-channel mutation causes isolated cardiac conduction diseaseH L Tan, M T Bink-Boelkens, C R Bezzina, et al.
Circulation|September 6, 2001
De novo mutation in the SCN5A gene associated with early onset of sudden infant deathH Wedekind, J P Smits, E Schulze-Bahr, et al.
Pageof 8