Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

R Bloise

Showing results (1-10 of 10) with videos related to

Pageof 1
Sort By:
Recenti Progressi in Medicina|February 24, 2001
[Genetic basis of sudden cardiac death]S G Priori, R Bloise
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 29, 2001
The long QT syndromeS G Priori, R Bloise, L Crotti
Circulation|August 30, 2000
The elusive link between LQT3 and Brugada syndrome: the role of flecainide challengeS G Priori, C Napolitano, P J Schwartz, et al.
Circulation|February 24, 2001
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardiaS G Priori, C Napolitano, N Tiso, 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.
Lancet (London, England)|October 31, 2001
Molecular diagnosis in a child with sudden infant death syndromeP J Schwartz, S G Priori, R Bloise, et al.
Cell Death & Disease|October 12, 2013
CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardiaE 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 familiesS G Priori, C Napolitano, M Gasparini, 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 populationN S Mok, S G Priori, C Napolitano, 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.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Recenti Progressi in Medicina|February 24, 2001
[Genetic basis of sudden cardiac death]S G Priori, R Bloise
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 29, 2001
The long QT syndromeS G Priori, R Bloise, L Crotti
Circulation|August 30, 2000
The elusive link between LQT3 and Brugada syndrome: the role of flecainide challengeS G Priori, C Napolitano, P J Schwartz, et al.
Circulation|February 24, 2001
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardiaS G Priori, C Napolitano, N Tiso, 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.
Lancet (London, England)|October 31, 2001
Molecular diagnosis in a child with sudden infant death syndromeP J Schwartz, S G Priori, R Bloise, et al.
Cell Death & Disease|October 12, 2013
CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardiaE 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 familiesS G Priori, C Napolitano, M Gasparini, 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 populationN S Mok, S G Priori, C Napolitano, 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.
Pageof 1