Background: This study examined the clinical characteristics, genetic basis, healthcare
utilisation and costs of catecholaminergic ventricular tachycardia (CPVT) patients from a …

Introduction Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare cardiac
ion channelopathy. The aim of this study is to examine the clinical characteristics, genetic …

Introduction Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare cardiac
ion channelopathy. The aim of this study is to examine the genetic basis and identify pre …

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare cardiac ion
channelopathy. This was the first systematic review of published works on the clinical …

Background—Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited
arrhythmia syndrome associated with mutations in the cardiac ryanodine receptor gene …

Background Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe
inherited arrhythmic disease associated with a risk of syncope and sudden cardiac death …

Objective The aim of this study was to characterise disease penetrance, course of disease
and use of antiarrhythmic medication and implantable cardioverter-defibrillator (ICD) therapy …

Background: The aim of the study was to assess underlying genetic cause (s), clinical
features, and response to therapy in catecholaminergic polymorphic ventricular tachycardia …

Background: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare,
inherited heart rhythm disorder that is caused by variants in genes responsible for cardiac …

Introduction: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare
inherited cardiac ion channelopathy. The present study aims to examine the clinical …