Drug-induced prolongation of the QT interval

DM Roden - New England Journal of Medicine, 2004 - Mass Medical Soc
The single most common cause of the withdrawal or restriction of the use of marketed drugs
has been QT-interval prolongation associated with polymorphic ventricular tachycardia, or …

Genetics of sudden cardiac death

CR Bezzina, N Lahrouchi, SG Priori - Circulation research, 2015 - Am Heart Assoc
Sudden cardiac death occurs in a broad spectrum of cardiac pathologies and is an important
cause of mortality in the general population. Genetic studies conducted during the past 20 …

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership …

MJ Ackerman, SG Priori, S Willems, C Berul… - Europace, 2011 - academic.oup.com
1From Mayo Clinic, Rochester, Minnesota; 2Fondazione Salvatore Maugeri University of
Pavia, Pavia, Italy and New York University, New York, New York; 3University Hospital …

Prevalence of the congenital long-QT syndrome

PJ Schwartz, M Stramba-Badiale, L Crotti… - Circulation, 2009 - Am Heart Assoc
Background—The prevalence of genetic arrhythmogenic diseases is unknown. For the long-
QT syndrome (LQTS), figures ranging from 1: 20 000 to 1: 5000 were published, but none …

[HTML][HTML] Risk stratification in the long-QT syndrome

SG Priori, PJ Schwartz, C Napolitano… - … England Journal of …, 2003 - Mass Medical Soc
Background Mutations in potassium-channel genes KCNQ1 (LQT1 locus) and KCNH2
(LQT2 locus) and the sodium-channel gene SCN5A (LQT3 locus) are the most common …

Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia

SG Priori, C Napolitano, N Tiso, M Memmi, G Vignati… - Circulation, 2001 - Am Heart Assoc
Background—Catecholaminergic polymorphic ventricular tachycardia is a genetic
arrhythmogenic disorder characterized by stress-induced, bidirectional ventricular …

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia

SG Priori, C Napolitano, M Memmi, B Colombi… - Circulation, 2002 - Am Heart Assoc
Background—Mutations in the cardiac ryanodine receptor gene (RyR2) underlie
catecholaminergic polymorphic ventricular tachycardia (CPVT), an inherited arrhythmogenic …

Task force on sudden cardiac death of the European Society of Cardiology

SG Priori, E Aliot, C Blomstrom-Lundqvist… - European heart …, 2001 - academic.oup.com
The members of the Task Force on Sudden Death dedicate this paper to the memory of our
former friend and colleague, Professor Ronald WF Campbell. Ronnie spent his life working …

Spectrum of Mutations in Long-QT Syndrome Genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

I Splawski, J Shen, KW Timothy, MH Lehmann… - Circulation, 2000 - Am Heart Assoc
Background—Long-QT Syndrome (LQTS) is a cardiovascular disorder characterized by
prolongation of the QT interval on ECG and presence of syncope, seizures, and sudden …

The long QT syndrome

PJ Schwartz - Current problems in cardiology, 1997 - Elsevier
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