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

Background and Purpose: This scientific statement provides an interprofessional,
comprehensive review of evidence and recommendations for indications, duration, and …

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 …

This consensus guideline was prepared on behalf of the International Society for Holter and
Noninvasive Electrocardiology and is cosponsored by the Japanese Circulation Society, the …

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 …

Background—The hypothesis that some cases of sudden infant death syndrome (SIDS)
could be caused by long-QT syndrome (LQTS) has been supported by molecular studies …

The implementation of video-based non-contact technologies to monitor the vital signs of
preterm infants in the hospital presents several challenges, such as the detection of the …

Congenital long QT syndrome (LQTS) is a hereditary cardiac disease characterized by a
prolongation of the QT interval at basal ECG and by a high risk of life-threatening …

Long QT syndrome (LQTS) refers to a group of “channelopathies”–disorders that affect
cardiac ion channels. The “family” concept of syndromes has been applied to the multiple …

Objective Aside from congenital heart block (CHB), sinus bradycardia and prolongation of
the corrected QT (QTc) interval have been reported in infants born to mothers with anti‐SSA …