Associated Papers
Voltage-Gated Sodium Channels: A Therapeutic Target in Ischemic Heart Disease.
Zhang XL et al.
Reviews in Cardiovascular Medicine, 2025
Complex interactions between p.His558Arg and linked variants in the sodium voltage-gated channel alpha subunit 5 (Na V 1.5).
Lopes-Marques M et al.
Peerj, 2022
Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction.
Foddha H et al.
Advances in Clinical and Experimental Medicine : Official Organ Wroclaw Medical University, 2020
Predicting changes to INa from missense mutations in human SCN5A.
Clerx M et al.
Scientific Reports, 2018
Cellular Mechanisms of Sinus Node Dysfunction in Carriers of the SCN5A-E161K Mutation and Role of the H558R Polymorphism.
Wilders R
Frontiers in Physiology, 2018
Compound Heterozygous SCN5A Mutations in a Toddler - Are they Associated with a More Severe Phenotype?
Sacilotto L et al.
Arquivos Brasileiros De Cardiologia, 2017
Epidemiology and genetics of ventricular fibrillation during acute myocardial infarction.
Glinge C et al.
Journal of Geriatric Cardiology : Jgc, 2016
Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect.
Veltmann C et al.
Journal of the American Heart Association, 2016
Unveiling specific triggers and precipitating factors for fatal cardiac events in inherited arrhythmia syndromes.
Nakajima T et al.
Circulation Journal : Official Journal of the Japanese Circulation Society, 2015
SCN5A mutations and polymorphisms in patients with ventricular fibrillation during acute myocardial infarction.
Boehringer T et al.
Molecular Medicine Reports, 2014
Identifying potential functional impact of mutations and polymorphisms: linking heart failure, increased risk of arrhythmias and sudden cardiac death.
Jagu B et al.
Frontiers in Physiology, 2013
Torsades de pointes following acute myocardial infarction: evidence for a deadly link with a common genetic variant.
Crotti L et al.
Heart Rhythm, 2012
Post myocardial ischemia-associated torsades de pointes in a patient carrying a KCNQ1 G643S variant.
Nakajima T et al.
Internal Medicine (tokyo, Japan), 2010
SCN5A mutation associated with acute myocardial infarction.
Oliva A et al.
Legal Medicine (tokyo, Japan), 2009
Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction.
Hu D et al.
Heart Rhythm, 2007
Genetic predisposition and cellular basis for ischemia-induced ST-segment changes and arrhythmias.
Hu D et al.
Journal of Electrocardiology, 0
Susceptibility genes & modifiers for cardiac arrhythmias.
Schulze-Bahr E
Progress in Biophysics and Molecular Biology, 0
Genetic variants in post myocardial infarction patients presenting with electrical storm of unstable ventricular tachycardia.
Rangaraju A et al.
Indian Pacing and Electrophysiology Journal, 0