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S G Priori

Showing results (51-60 of 85) with videos related to

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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.
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.
The New England Journal of Medicine|July 27, 2000
A molecular link between the sudden infant death syndrome and the long-QT syndromeP J Schwartz, S G Priori, R Dumaine, 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.
European Heart Journal|November 1, 1992
Unexplained cardiac arrest. The need for a prospective registryS G Priori, M Borggrefe, A J Camm, et al.
Pageof 9

Showing results (51-60 of 85) with videos related to

Sort By:
Pageof 9
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.
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.
The New England Journal of Medicine|July 27, 2000
A molecular link between the sudden infant death syndrome and the long-QT syndromeP J Schwartz, S G Priori, R Dumaine, 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.
European Heart Journal|November 1, 1992
Unexplained cardiac arrest. The need for a prospective registryS G Priori, M Borggrefe, A J Camm, et al.
Pageof 9