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Duodecim; Laaketieteellinen Aikakauskirja
|
January 1, 1991
[Arrhythmogenic right ventricular dysplasia and idiopathic tachycardia]
H Parikka, L Toivonen, M Viitasalo, et al.
The American Journal of Cardiology
|
September 25, 1999
QT interval and QT dispersion in endurance athletes and in power athletes using large doses of anabolic steroids
A Stolt, T Karila, M Viitasalo, et al.
The American Journal of Cardiology
|
February 15, 1997
Effects of acute alcohol ingestion on heart rate variability in patients with documented coronary artery disease and stable angina pectoris
J Rossinen, M Viitasalo, J Partanen, et al.
Human Genetics
|
October 1, 1995
Linkage of the long QT syndrome to the short arm of chromosome 11: use of five highly polymorphic markers towards more detailed localization of the mutant gene
K Kainulainen, H Swan, H Miettinen, et al.
Journal of the American College of Cardiology
|
August 10, 1999
Angiotensinogen gene M235T polymorphism predicts left ventricular hypertrophy in endurance athletes
J Karjalainen, U M Kujala, A Stolt, et al.
European Heart Journal
|
May 1, 1994
Left ventricular function in children with the Marfan syndrome
A Savolainen, L Nisula, P Keto, et al.
Pacing and Clinical Electrophysiology : PACE
|
October 30, 1998
Magnetocardiographic QT interval dispersion in postmyocardial infarction patients with sustained ventricular tachycardia: validation of automated QT measurements
L Oikarinen, M Paavola, J Montonen, et al.
The American Journal of Cardiology
|
March 29, 2001
Effect of the antimalarial drug halofantrine in the long QT syndrome due to a mutation of the cardiac sodium channel gene SCN5A
K Piippo, S Holmström, H Swan, et al.
Circulation
|
August 8, 2007
Prevalence and prognostic significance of short QT interval in a middle-aged Finnish population
O Anttonen, M J Junttila, H Rissanen, et al.
Human Mutation
|
June 22, 2000
Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects
P Laitinen, H Fodstad, K Piippo, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 69) with videos related to
Sort By:
Page
of 7
Duodecim; Laaketieteellinen Aikakauskirja
|
January 1, 1991
[Arrhythmogenic right ventricular dysplasia and idiopathic tachycardia]
H Parikka, L Toivonen, M Viitasalo, et al.
The American Journal of Cardiology
|
September 25, 1999
QT interval and QT dispersion in endurance athletes and in power athletes using large doses of anabolic steroids
A Stolt, T Karila, M Viitasalo, et al.
The American Journal of Cardiology
|
February 15, 1997
Effects of acute alcohol ingestion on heart rate variability in patients with documented coronary artery disease and stable angina pectoris
J Rossinen, M Viitasalo, J Partanen, et al.
Human Genetics
|
October 1, 1995
Linkage of the long QT syndrome to the short arm of chromosome 11: use of five highly polymorphic markers towards more detailed localization of the mutant gene
K Kainulainen, H Swan, H Miettinen, et al.
Journal of the American College of Cardiology
|
August 10, 1999
Angiotensinogen gene M235T polymorphism predicts left ventricular hypertrophy in endurance athletes
J Karjalainen, U M Kujala, A Stolt, et al.
European Heart Journal
|
May 1, 1994
Left ventricular function in children with the Marfan syndrome
A Savolainen, L Nisula, P Keto, et al.
Pacing and Clinical Electrophysiology : PACE
|
October 30, 1998
Magnetocardiographic QT interval dispersion in postmyocardial infarction patients with sustained ventricular tachycardia: validation of automated QT measurements
L Oikarinen, M Paavola, J Montonen, et al.
The American Journal of Cardiology
|
March 29, 2001
Effect of the antimalarial drug halofantrine in the long QT syndrome due to a mutation of the cardiac sodium channel gene SCN5A
K Piippo, S Holmström, H Swan, et al.
Circulation
|
August 8, 2007
Prevalence and prognostic significance of short QT interval in a middle-aged Finnish population
O Anttonen, M J Junttila, H Rissanen, et al.
Human Mutation
|
June 22, 2000
Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects
P Laitinen, H Fodstad, K Piippo, et al.
Page
of 7