Idiopathic ventricular fibrillation: the ongoing quest for diagnostic refinement

Prevalence and electrophysiological phenotype of rare SCN5A genetic variants identified in unexplained sudden cardiac arrest survivors

(2020) John R Giudicessi et al.   EUROPACE

Initially Unexplained Cardiac Arrest in Children and Adolescents: A National Experience from the Canadian Pediatric Heart Rhythm Network

(2020) Taylor Cunningham et al.   HEART RHYTHM

Identification of a Novel Homozygous Multi-Exon Duplication in RYR2 Among Children With Exertion-Related Unexplained Sudden Deaths in the Amish Community

(2020) David J. Tester et al.   JAMA Cardiology

Exercise testing oversights underlie missed and delayed diagnosis of catecholaminergic polymorphic ventricular tachycardia in young sudden cardiac arrest survivors

(2019) John R. Giudicessi et al.   HEART RHYTHM

Idiopathic ventricular fibrillation with repetitive activity inducible within the distal Purkinje system

(2019) Michel Haissaguerre et al.   HEART RHYTHM

Long‐Term Follow‐Up of Idiopathic Ventricular Fibrillation in a Pediatric Population: Clinical Characteristics, Management, and Complications

(2019) Antonio Frontera et al.   Journal of the American Heart Association

Out-of-hospital cardiac arrest due to idiopathic ventricular fibrillation in patients with normal electrocardiograms: results from a multicentre long-term registry

(2019) Giulio Conte et al.   EUROPACE

Primary Myocardial Fibrosis as an Alternative Phenotype Pathway of Inherited Cardiac Structural Disorders

(2018) M. Juhani Junttila et al.   CIRCULATION

Localized Structural Alterations Underlying a Subset of Unexplained Sudden Cardiac Death

(2018) Michel Haïssaguerre et al.   Circulation-Arrhythmia and Electrophysiology

Characteristics and clinical assessment of unexplained sudden cardiac arrest in the real-world setting: focus on idiopathic ventricular fibrillation

(2018) Victor Waldmann et al.   EUROPEAN HEART JOURNAL

Role of genetic heart disease in sentinel sudden cardiac arrest survivors across the age spectrum

(2018) John R. Giudicessi et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia?

(2018) Jaakko T. Leinonen et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

The Diagnostic Yield of Brugada Syndrome After Sudden Death With Normal Autopsy

(2018) Michael Papadakis et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Suppression-of-function mutations in the cardiac ryanodine receptor: Emerging evidence for a novel arrhythmia syndrome?

(2017) Thomas M. Roston et al.   HEART RHYTHM

Next-generation sequencing of a large gene panel in patients initially diagnosed with idiopathic ventricular fibrillation

(2017) Marloes Visser et al.   HEART RHYTHM

Genetic Testing in the Evaluation of Unexplained Cardiac ArrestCLINICAL PERSPECTIVE

(2017) Greg Mellor et al.   Circulation-Cardiovascular Genetics

Genetic defects in a His-Purkinje system transcription factor,IRX3, cause lethal cardiac arrhythmias

(2015) Akiko Koizumi et al.   EUROPEAN HEART JOURNAL

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Follow-up From Childhood to Adulthood of Individuals With Family History of Brugada Syndrome and Normal Electrocardiograms

(2014) Giulio Conte et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

(2013) Lia Crotti et al.   CIRCULATION

Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes

(2013) Silvia G. Priori et al.   EUROPACE

The long QT syndrome: a transatlantic clinical approach to diagnosis and therapy

(2013) P. J. Schwartz et al.   EUROPEAN HEART JOURNAL

Familial cardiological and targeted genetic evaluation: Low yield in sudden unexplained death and high yield in unexplained cardiac arrest syndromes

(2013) Saurabh Kumar et al.   HEART RHYTHM

Evolution of clinical diagnosis in patients presenting with unexplained cardiac arrest or syncope due to polymorphic ventricular tachycardia

(2013) Maria Vittoria Matassini et al.   HEART RHYTHM

New Clinical and Electrocardiographic Classification in Patients with Idiopathic Ventricular Fibrillation

(2013) YUKIO SEKIGUCHI et al.   JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY

A Mutation in CALM1 Encoding Calmodulin in Familial Idiopathic Ventricular Fibrillation in Childhood and Adolescence

(2013) Roos F. Marsman et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

A ressonância magnética cardíaca como uma mais-valia no diagnóstico etiológico de arritmias ventriculares

(2013) Nuno Cabanelas et al.   Revista Portuguesa de Cardiologia

Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

(2012) Mette Nyegaard et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Idiopathic Ventricular Fibrillation, Early Repolarization and Other J Wave-Related Ventricular Fibrillation Syndromes

(2012) Gi-Byoung Nam   CIRCULATION JOURNAL

HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)

(2011) M. J. Ackerman et al.   EUROPACE

Unexplained Drownings and the Cardiac Channelopathies: A Molecular Autopsy Series

(2011) David J. Tester et al.   MAYO CLINIC PROCEEDINGS

Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation

(2009) Marielle Alders et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Systematic Assessment of Patients With Unexplained Cardiac Arrest

(2009) Andrew D. Krahn et al.   CIRCULATION

Sudden Cardiac Arrest Associated with Early Repolarization

(2008) Michel Haïssaguerre et al.   NEW ENGLAND JOURNAL OF MEDICINE