The main inherited cardiac arrhythmias are long QT syndrome, short QT syndrome,
catecholaminergic polymorphic ventricular tachycardia and Brugada syndrome. These rare …

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 …

1From Mayo Clinic, Rochester, Minnesota; 2Fondazione Salvatore Maugeri University of
Pavia, Pavia, Italy and New York University, New York, New York; 3University Hospital …

Background: Heart rate–corrected QT interval (QTc) prolongation, whether secondary to
drugs, genetics including congenital long QT syndrome, and/or systemic diseases including …

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 …

Sudden unexpected death in epilepsy (SUDEP) is the leading cause of death in patients
with refractory epilepsy, with an estimated 35% lifetime risk in this patient population. There …

Airmail rates available on request.* Canadian 7% Goods and Services Tax, calculated on
US base rate, has been added and will be paid by Mosby to Revenue Canada under GST …

This chapter summarizes the recent advances in the neuropathology of sudden infant death
syndrome (SIDS). In 2015, hippocampal abnormalities were described in SIDS infants …

Although largely neglected in earlier literature, sudden unexpected death in epilepsy
(SUDEP) is the most important epilepsy-related mode of death, and is the leading cause of …

The hereditary Long QT syndrome (LQTS) is a genetic channelopathy with variable
penetrance that is associated with increased propensity for polymorphic ventricular …