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Circulation|June 26, 1998
A recessive variant of the Romano-Ward long-QT syndrome?S G Priori, P J Schwartz, C Napolitano, et al.The Journal of Biological Chemistry|June 19, 2001
Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypesI Rivolta, H Abriel, M Tateyama, et al.American Journal of Physiology. Heart and Circulatory Physiology|November 22, 2000
Mechanisms of I(Ks) suppression in LQT1 mutantsL Bianchi, S G Priori, C Napolitano, et al.Circulation Research|April 17, 2001
Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channelH Abriel, C Cabo, X H Wehrens, et al.Human Molecular Genetics|July 13, 1999
Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndromeL Bianchi, Z Shen, A T Dennis, et al.Italian Heart Journal : Official Journal of the Italian Federation of Cardiology|June 1, 2000
Gene-specific differences in the circadian variation of ventricular repolarization in the long QT syndrome: a key to sudden death during sleep?M Stramba-Badiale, S G Priori, C Napolitano, et al.The American Journal of Physiology|June 1, 1990
Mechanisms underlying early and delayed afterdepolarizations induced by catecholaminesS G Priori, P B CorrCardiologia (Rome, Italy)|March 1, 1991
[Variations in arrhythmogenic response to catecholamines in acute myocardial ischemia]S G Priori, P B CorrLancet (London, England)|October 31, 2001
Molecular diagnosis in a child with sudden infant death syndromeP J Schwartz, S G Priori, R Bloise, et al.Circulation|July 1, 1988
Delayed afterdepolarizations elicited in vivo by left stellate ganglion stimulationS G Priori, M Mantica, P J SchwartzPageof 14