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Nature Genetics
|
September 2, 1999
Cardiac conduction defects associate with mutations in SCN5A
J 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 fibers
J 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 fibrillation
N 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 syndrome
M 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 gene
M 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+ channels
B 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 correlation
J 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 disease
H 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 death
H Wedekind, J P Smits, E Schulze-Bahr, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 78) with videos related to
Sort By:
Page
of 8
Nature Genetics
|
September 2, 1999
Cardiac conduction defects associate with mutations in SCN5A
J 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 fibers
J 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 fibrillation
N 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 syndrome
M 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 gene
M 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+ channels
B 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 correlation
J 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 disease
H 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 death
H Wedekind, J P Smits, E Schulze-Bahr, et al.
Page
of 8