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Proceedings of the National Academy of Sciences of the United States of America
|
September 14, 2000
A common polymorphism associated with antibiotic-induced cardiac arrhythmia
F Sesti, G W Abbott, J Wei, et al.
Human Genetics
|
April 18, 2007
Gene symbol: SCN5A
L Crotti, C Ferrandi, R Insolia, et al.
Human Genetics
|
April 18, 2007
Gene symbol: KCNQ1
L Crotti, R Insolia, M Pedrazzini, et al.
Circulation
|
December 15, 1995
Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy
P J Schwartz, S G Priori, E H Locati, et al.
Journal of the American College of Cardiology
|
November 6, 2001
Sympathetic stimulation produces a greater increase in both transmural and spatial dispersion of repolarization in LQT1 than LQT2 forms of congenital long QT syndrome
Y Tanabe, M Inagaki, T Kurita, et al.
European Heart Journal
|
November 27, 2002
Proposed diagnostic criteria for the Brugada syndrome
A A M Wilde, C Antzelevitch, M Borggrefe, et al.
Circulation
|
March 17, 1999
Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome
Q Chen, D Zhang, R L Gingell, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
September 29, 2000
Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome
E Ficker, D Thomas, P C Viswanathan, et al.
European Heart Journal
|
June 19, 2002
Gene-specific response of dynamic ventricular repolarization to sympathetic stimulation in LQT1, LQT2 and LQT3 forms of congenital long QT syndrome
T Noda, H Takaki, T Kurita, et al.
European Heart Journal
|
March 19, 1999
Genetic and molecular basis of cardiac arrhythmias; impact on clinical management. Study group on molecular basis of arrhythmias of the working group on arrhythmias of the european society of cardiology
S G Priori, J Barhanin, R N Hauer, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 95) with videos related to
Sort By:
Page
of 10
Proceedings of the National Academy of Sciences of the United States of America
|
September 14, 2000
A common polymorphism associated with antibiotic-induced cardiac arrhythmia
F Sesti, G W Abbott, J Wei, et al.
Human Genetics
|
April 18, 2007
Gene symbol: SCN5A
L Crotti, C Ferrandi, R Insolia, et al.
Human Genetics
|
April 18, 2007
Gene symbol: KCNQ1
L Crotti, R Insolia, M Pedrazzini, et al.
Circulation
|
December 15, 1995
Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy
P J Schwartz, S G Priori, E H Locati, et al.
Journal of the American College of Cardiology
|
November 6, 2001
Sympathetic stimulation produces a greater increase in both transmural and spatial dispersion of repolarization in LQT1 than LQT2 forms of congenital long QT syndrome
Y Tanabe, M Inagaki, T Kurita, et al.
European Heart Journal
|
November 27, 2002
Proposed diagnostic criteria for the Brugada syndrome
A A M Wilde, C Antzelevitch, M Borggrefe, et al.
Circulation
|
March 17, 1999
Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome
Q Chen, D Zhang, R L Gingell, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
September 29, 2000
Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome
E Ficker, D Thomas, P C Viswanathan, et al.
European Heart Journal
|
June 19, 2002
Gene-specific response of dynamic ventricular repolarization to sympathetic stimulation in LQT1, LQT2 and LQT3 forms of congenital long QT syndrome
T Noda, H Takaki, T Kurita, et al.
European Heart Journal
|
March 19, 1999
Genetic and molecular basis of cardiac arrhythmias; impact on clinical management. Study group on molecular basis of arrhythmias of the working group on arrhythmias of the european society of cardiology
S G Priori, J Barhanin, R N Hauer, et al.
Page
of 10