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S G Priori
R Bloise
L Crotti

Showing results (71-80 of 95) with videos related to

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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 arrhythmiaF Sesti, G W Abbott, J Wei, et al.
Human Genetics|April 18, 2007
Gene symbol: SCN5AL Crotti, C Ferrandi, R Insolia, et al.
Human Genetics|April 18, 2007
Gene symbol: KCNQ1L 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 therapyP 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 syndromeY Tanabe, M Inagaki, T Kurita, et al.
European Heart Journal|November 27, 2002
Proposed diagnostic criteria for the Brugada syndromeA A M Wilde, C Antzelevitch, M Borggrefe, et al.
Circulation|March 17, 1999
Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndromeQ 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 syndromeE 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 syndromeT 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 cardiologyS G Priori, J Barhanin, R N Hauer, et al.
Pageof 10

Showing results (71-80 of 95) with videos related to

Sort By:
Pageof 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 arrhythmiaF Sesti, G W Abbott, J Wei, et al.
Human Genetics|April 18, 2007
Gene symbol: SCN5AL Crotti, C Ferrandi, R Insolia, et al.
Human Genetics|April 18, 2007
Gene symbol: KCNQ1L 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 therapyP 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 syndromeY Tanabe, M Inagaki, T Kurita, et al.
European Heart Journal|November 27, 2002
Proposed diagnostic criteria for the Brugada syndromeA A M Wilde, C Antzelevitch, M Borggrefe, et al.
Circulation|March 17, 1999
Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndromeQ 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 syndromeE 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 syndromeT 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 cardiologyS G Priori, J Barhanin, R N Hauer, et al.
Pageof 10