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Lancet (London, England)
|
October 31, 2001
Molecular diagnosis in a child with sudden infant death syndrome
P J Schwartz, S G Priori, R Bloise, et al.
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.
Cell Death & Disease
|
October 12, 2013
CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardia
E Di Pasquale, F Lodola, M Miragoli, et al.
Circulation
|
November 15, 2000
Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families
S G Priori, C Napolitano, M Gasparini, 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.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi
|
February 18, 2004
Clinical profile and genetic basis of Brugada syndrome in the Chinese population
N S Mok, S G Priori, C Napolitano, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 85) with videos related to
Sort By:
Page
of 9
Lancet (London, England)
|
October 31, 2001
Molecular diagnosis in a child with sudden infant death syndrome
P J Schwartz, S G Priori, R Bloise, et al.
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.
Cell Death & Disease
|
October 12, 2013
CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardia
E Di Pasquale, F Lodola, M Miragoli, et al.
Circulation
|
November 15, 2000
Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families
S G Priori, C Napolitano, M Gasparini, 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.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi
|
February 18, 2004
Clinical profile and genetic basis of Brugada syndrome in the Chinese population
N S Mok, S G Priori, C Napolitano, et al.
Page
of 9