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Journal of Cardiovascular Electrophysiology|June 27, 2000
Evidence for a cardiac ion channel mutation underlying drug-induced QT prolongation and life-threatening arrhythmiasC Napolitano, P J Schwartz, A M Brown, et al.Circulation|December 31, 1997
Evaluation of the spatial aspects of T-wave complexity in the long-QT syndromeS G Priori, D W Mortara, C Napolitano, et al.The Annals of Thoracic Surgery|August 1, 1988
Computerized global electrophysiological mapping of the atrium in a patient with multiple supraventricular tachyarrhythmiasT E Canavan, R B Schuessler, M E Cain, et al.Journal of Electrocardiology|July 1, 1991
Evidence that cocaine slows cardiac conduction by an action on both AV nodal and His-Purkinje tissue in the dogC M Tracy, L Bachenheimer, A Solomon, 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.Circulation|June 26, 1998
A recessive variant of the Romano-Ward long-QT syndrome?S G Priori, P J Schwartz, C Napolitano, et al.American Journal of Rhinology|July 7, 1999
Cardiovascular safety of second-generation antihistaminesJ T Barbey, M Anderson, G Ciprandi, et al.Human Molecular Genetics|September 1, 1995
Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmiaQ Wang, J Shen, Z Li, 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.Pageof 15