Short-coupled ventricular fibrillation represents a distinct phenotype among latent causes of unexplained cardiac arrest: a report from the CASPER registry
Published 2021 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Short-coupled ventricular fibrillation represents a distinct phenotype among latent causes of unexplained cardiac arrest: a report from the CASPER registry
Authors
Keywords
-
Journal
EUROPEAN HEART JOURNAL
Volume -, Issue -, Pages -
Publisher
Oxford University Press (OUP)
Online
2021-04-28
DOI
10.1093/eurheartj/ehab275
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- The mutational constraint spectrum quantified from variation in 141,456 humans
- (2020) Konrad J. Karczewski et al. NATURE
- An International Multi-Center Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2 - Catecholaminergic Polymorphic Ventricular Tachycardia
- (2020) Kevin Ng et al. CIRCULATION
- Quinidine-Responsive Polymorphic Ventricular Tachycardia in Patients with Coronary Heart Disease
- (2019) Sami Viskin et al. CIRCULATION
- Incidence and predictors of implantable cardioverter-defibrillator therapy and its complications in idiopathic ventricular fibrillation patients
- (2019) Lennart J Blom et al. EUROPACE
- Mapping and Ablation of Ventricular Fibrillation Associated with Early Repolarization Syndrome
- (2019) Koonlawee Nademanee et al. CIRCULATION
- 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
- Quinidine-responsive out-of-hospital polymorphic ventricular tachycardia in patients with coronary heart disease
- (2019) Sami Viskin et al. EUROPACE
- Localized Structural Alterations Underlying a Subset of Unexplained Sudden Cardiac Death
- (2018) Michel Haïssaguerre et al. Circulation-Arrhythmia and Electrophysiology
- Four TRPM4 Cation Channel Mutations Found in Cardiac Conduction Diseases Lead to Altered Protein Stability
- (2018) Beatrice Bianchi et al. Frontiers in Physiology
- VarSome: the human genomic variant search engine
- (2018) Christos Kopanos et al. BIOINFORMATICS
- Next-generation sequencing of a large gene panel in patients initially diagnosed with idiopathic ventricular fibrillation
- (2017) Marloes Visser et al. HEART RHYTHM
- The QUIDAM study: Hydroquinidine therapy for the management of Brugada syndrome patients at high arrhythmic risk
- (2017) Antoine Andorin et al. HEART RHYTHM
- Hydroquinidine Prevents Life-Threatening Arrhythmic Events in Patients With Short QT Syndrome
- (2017) Andrea Mazzanti et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- ClinVar: improving access to variant interpretations and supporting evidence
- (2017) Melissa J Landrum et al. NUCLEIC ACIDS RESEARCH
- Cardiac Abnormalities in First-Degree Relatives of Unexplained Cardiac Arrest Victims
- (2016) Christian Steinberg et al. Circulation-Arrhythmia and Electrophysiology
- Idiopathic Ventricular Fibrillation
- (2016) Marloes Visser et al. Circulation-Arrhythmia and Electrophysiology
- Detailed characterization of familial idiopathic ventricular fibrillation linked to the DPP6 locus
- (2016) Judith N. ten Sande et al. HEART RHYTHM
- A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia
- (2016) Belinda Gray et al. HEART RHYTHM
- J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge
- (2016) Charles Antzelevitch et al. HEART RHYTHM
- Short-Coupled Ventricular Fibrillation: Concealed Purkinje Depolarization
- (2016) GREG MELLOR et al. JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY
- Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives
- (2015) C. Semsarian et al. EUROPEAN HEART JOURNAL
- Genetic defects in a His-Purkinje system transcription factor,IRX3, cause lethal cardiac arrhythmias
- (2015) Akiko Koizumi et al. EUROPEAN HEART JOURNAL
- The Early Repolarization Pattern
- (2015) Peter W. Macfarlane et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Use of Whole Exome Sequencing for the Identification of Ito-Based Arrhythmia Mechanism and Therapy
- (2015) A. C. Sturm et al. Journal of the American Heart Association
- Nonsense Mutations in BAG3 are Associated With Early-Onset Dilated Cardiomyopathy in French Canadians
- (2014) Nathalie Chami et al. CANADIAN JOURNAL OF CARDIOLOGY
- MutationTaster2: mutation prediction for the deep-sequencing age
- (2014) Jana Marie Schwarz et al. NATURE METHODS
- Ryanodine Receptor Mutations Presenting as Idiopathic Ventricular Fibrillation: A Report on Two Novel Familial Compound Mutations, c.6224T>C and c.13781A>G, With the Clinical Presentation of Idiopathic Ventricular Fibrillation
- (2014) Christian Paech et al. PEDIATRIC CARDIOLOGY
- Unique Cardiac Purkinje Fiber Transient Outward Current β-Subunit Composition
- (2013) Ling Xiao et al. CIRCULATION RESEARCH
- Ventricular fibrillation associated with complete right bundle branch block
- (2013) Yoshiyasu Aizawa et al. HEART RHYTHM
- HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes
- (2013) Silvia G. Priori et al. HEART RHYTHM
- Quinidine, A Life-Saving Medication for Brugada Syndrome, Is Inaccessible in Many Countries
- (2013) Sami Viskin et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- 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
- SIFT web server: predicting effects of amino acid substitutions on proteins
- (2012) Ngak-Leng Sim et al. NUCLEIC ACIDS RESEARCH
- Predicting the effects of frameshifting indels
- (2012) Jing Hu et al. GENOME BIOLOGY
- Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6
- (2011) P. G. Postema et al. Netherlands Heart Journal
- 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
- Mode of onset of ventricular fibrillation in patients with early repolarization pattern vs. Brugada syndrome
- (2009) G.-B. Nam et al. EUROPEAN HEART JOURNAL
- Long-Term Follow-Up of Idiopathic Ventricular Fibrillation Ablation
- (2009) Sébastien Knecht et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Excellent Long-Term Reproducibility of the Electrophysiologic Efficacy of Quinidine in Patients with Idiopathic Ventricular Fibrillation and Brugada Syndrome
- (2009) BERNARD BELHASSEN et al. PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreDiscover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversation