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S G Priori
R Bloise
L Crotti

Showing results (61-70 of 95) with videos related to

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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.
Revista Da Associacao Medica Brasileira (1992)|August 12, 1998
[Polyalveolosis: pathogenesis of congenital lobar emphysema?]R Giudici, L E Leão, L A Moura, 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.
Circulation|January 4, 2001
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmiasP J Schwartz, S G Priori, C Spazzolini, et al.
Human Genetics|October 21, 2010
Gene symbol: KCNH2. Disease: Long QT syndromeLia Crotti, L Crotti, M Pedrazzini, et al.
Human Genetics|April 18, 2007
Gene symbol: KCNH2L Crotti, R Insolia, M Pedrazzini, et al.
Human Genetics|April 18, 2007
Gene symbol: KCNH2L Crotti, M Pedrazzini, C Ferrandi, et al.
Human Genetics|April 18, 2007
Gene symbol: SCN5AL Crotti, C Ferrandi, R Insolia, et al.
Pageof 10

Showing results (61-70 of 95) with videos related to

Sort By:
Pageof 10
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.
Revista Da Associacao Medica Brasileira (1992)|August 12, 1998
[Polyalveolosis: pathogenesis of congenital lobar emphysema?]R Giudici, L E Leão, L A Moura, 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.
Circulation|January 4, 2001
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmiasP J Schwartz, S G Priori, C Spazzolini, et al.
Human Genetics|October 21, 2010
Gene symbol: KCNH2. Disease: Long QT syndromeLia Crotti, L Crotti, M Pedrazzini, et al.
Human Genetics|April 18, 2007
Gene symbol: KCNH2L Crotti, R Insolia, M Pedrazzini, et al.
Human Genetics|April 18, 2007
Gene symbol: KCNH2L Crotti, M Pedrazzini, C Ferrandi, et al.
Human Genetics|April 18, 2007
Gene symbol: SCN5AL Crotti, C Ferrandi, R Insolia, et al.
Pageof 10