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

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

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 …

Backgrounds Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare but
lethal cardiac ion channelopathy. Delayed diagnosis and misdiagnosis remain a matter of …

Background Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare and
lethal arrhythmia. Ryanodine receptor 2 (RYR2) mutation accounts for∼ 60% of CPVT …

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

Background: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare
inherited disorder causing life-threatening arrhythmias. Long-term outcome studies of the …

Background: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an
arrhythmo-genic cardiac disease predisposing affected individuals to sudden cardiac death …

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited arrhythmia
syndrome characterised by adenergically mediated bidirectional and/or polymorphic …