ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: a report of the American College …

Developed in Collaboration With the European … - Journal of the American …, 2006 - jacc.org
ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and
the Prevention of Sudden Cardiac Death: A Report of the American College of …

Basic mechanisms of cardiac impulse propagation and associated arrhythmias

AG Kléber, Y Rudy - Physiological reviews, 2004 - journals.physiology.org
Kléber, André G., and Yoram Rudy. Basic Mechanisms of Cardiac Impulse Propagation and
Associated Arrhythmias. Physiol Rev 84: 431–488, 2004; 10.1152/physrev. 00025.2003 …

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 …

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias

PJ Schwartz, SG Priori, C Spazzolini, AJ Moss… - Circulation, 2001 - Am Heart Assoc
Background—The congenital long-QT syndrome (LQTS) is caused by mutations on several
genes, all of which encode cardiac ion channels. The progressive understanding of the …

[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 …

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 …

Recommendations for competitive sports participation in athletes with cardiovascular disease: a consensus document from the Study Group of Sports Cardiology of …

A Pelliccia, R Fagard, HH Bjørnstad… - European heart …, 2005 - academic.oup.com
The rationale for offering an expert consensus document concerning the participation in
competitive sports by individuals with cardiovascular (CV) disease is based on the widely …

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 …

Short QT syndrome: a familial cause of sudden death

F Gaita, C Giustetto, F Bianchi, C Wolpert, R Schimpf… - Circulation, 2003 - Am Heart Assoc
Background—A prolonged QT interval is associated with a risk for life-threatening events.
However, little is known about prognostic implications of the reverse—a short QT interval …

Pharmacogenetics and adverse drug reactions

UA Meyer - The Lancet, 2000 - thelancet.com
Polymorphisms in the genes that code for drug-metabolising enzymes, drug transporters,
drug receptors, and ion channels can affect an individual's risk of having an adverse drug …