S G Priori|C Napolitano - JoVE Visualize

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American Heart Journal|July 1, 1988

Ventricular fibrillation induced by the interaction between acute myocardial ischemia and sympathetic hyperactivity: effect of nifedipineS G Priori, G Zuanetti, P J Schwartz

Schweizerische Medizinische Wochenschrift|October 12, 1996

The long QT syndrome: new diagnostic and therapeutic approach in the era of molecular biologyS G Priori, F Cantù, P J Schwartz

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|January 1, 1991

Influence of hypoxia on adrenergic modulation of triggered activity in isolated adult canine myocytesS G Priori, K A Yamada, P B Corr

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.

Circulation|December 15, 1995

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapyP J Schwartz, S G Priori, E H Locati, et al.

Giornale Italiano Di Cardiologia|February 1, 1995

[Idiopathic ventricular fibrillation: from a collection of clinical cases to a prospective evaluation. The U-CARE Steering Committee. Unexplained Cardiac Arrest Registry of Europe]S G Priori, V Paganini, L Boccalatte, et al.

Circulation|March 17, 1999

Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndromeQ Chen, D Zhang, R L Gingell, et al.

American Journal of Physiology. Heart and Circulatory Physiology|September 29, 2000

Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndromeE Ficker, D Thomas, P C Viswanathan, 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.

Pageof 14

Showing results (31-40 of 132) with videos related to

Sort By:

Pageof 14

American Heart Journal|July 1, 1988

Ventricular fibrillation induced by the interaction between acute myocardial ischemia and sympathetic hyperactivity: effect of nifedipineS G Priori, G Zuanetti, P J Schwartz

Schweizerische Medizinische Wochenschrift|October 12, 1996

The long QT syndrome: new diagnostic and therapeutic approach in the era of molecular biologyS G Priori, F Cantù, P J Schwartz

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|January 1, 1991

Influence of hypoxia on adrenergic modulation of triggered activity in isolated adult canine myocytesS G Priori, K A Yamada, P B Corr

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.

Circulation|December 15, 1995

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapyP J Schwartz, S G Priori, E H Locati, et al.

Giornale Italiano Di Cardiologia|February 1, 1995

[Idiopathic ventricular fibrillation: from a collection of clinical cases to a prospective evaluation. The U-CARE Steering Committee. Unexplained Cardiac Arrest Registry of Europe]S G Priori, V Paganini, L Boccalatte, et al.

Circulation|March 17, 1999

Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndromeQ Chen, D Zhang, R L Gingell, et al.

American Journal of Physiology. Heart and Circulatory Physiology|September 29, 2000

Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndromeE Ficker, D Thomas, P C Viswanathan, 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.

Pageof 14