Differential Diagnosis Between Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Type 1 ― Modified Schwartz Score ―
Authors:
Open Access
- 24 August 2018
- journal article
- research article
- Published by Japanese Circulation Society in Circulation Journal
- Vol. 82 (9) , 2269-2276
Abstract
Japan's largest platform for academic e-journals: J-STAGE is a full text database for reviewed academic papers published by Japanese societiesKeywords
This publication has 32 references indexed in Scilit:
- Catecholaminergic Polymorphic Ventricular TachycardiaCirculation: Arrhythmia and Electrophysiology, 2012
- Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac DeathThe American Journal of Human Genetics, 2012
- Cardiac Channel Molecular Autopsy: Insights From 173 Consecutive Cases of Autopsy-Negative Sudden Unexplained Death Referred for Postmortem Genetic TestingMayo Clinic Proceedings, 2012
- Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in humanHuman Molecular Genetics, 2012
- Genetic Testing for Potentially Lethal, Highly Treatable Inherited Cardiomyopathies/Channelopathies in Clinical PracticeCirculation, 2011
- Long QT SyndromeJACC, 2008
- Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testingHeart Rhythm, 2005
- Catecholaminergic polymorphic ventricular tachycardia: electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden deathHeart, 2003
- Clinical and Molecular Characterization of Patients With Catecholaminergic Polymorphic Ventricular TachycardiaCirculation, 2002
- Genotype-Phenotype Correlation in the Long-QT SyndromeCirculation, 2001