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Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

https://doi.org/10.1172/jci200318062

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/geno.1996.0236openalex-snapshot

Genomic Organization of the HumanSCN5AGene Encoding the Cardiac Sodium Channel

inferredcites →https://doi.org/10.1007/bf00273316openalex-snapshot

Heterozygote manifestation in recessive generalized myotonia

inferredcites →https://doi.org/10.1016/0002-8703(91)90281-lopenalex-snapshot

Postextrasystolic sinoatrial exit block in human sick sinus syndrome: Demonstration by direct recording of sinus node electrograms

inferredcites →https://doi.org/10.1016/0002-9149(83)90358-2openalex-snapshot

Symptomatic sick sinus syndrome in children and adolescents as the only manifestation of cardiac abnormality or associated with unoperated congenital heart disease

inferredcites →https://doi.org/10.1016/0002-9149(84)90540-xopenalex-snapshot

Familial atrial standstill and inexcitability in childhood

inferredcites →https://doi.org/10.1016/0092-8674(95)90359-3openalex-snapshot

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

inferredcites →https://doi.org/10.1016/s0002-8703(76)80334-1openalex-snapshot

Spectrum of sinus node dysfunction in two siblings

inferredcites →https://doi.org/10.1016/s0008-6363(00)00006-7openalex-snapshot

Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes

inferredcites →https://doi.org/10.1016/s0008-6363(99)00031-0openalex-snapshot

Structure and function of the cardiac sodium channels

inferredcites →https://doi.org/10.1016/s0014-5793(98)00033-7openalex-snapshot

A de novo missense mutation of human cardiac Na+ channel exhibiting novel molecular mechanisms of long QT syndrome

inferredcites →https://doi.org/10.1016/s0896-6273(00)81133-2openalex-snapshot

From Ionic Currents to Molecular Mechanisms

inferredcites →https://doi.org/10.1038/12618openalex-snapshot

Cardiac conduction defects associate with mutations in SCN5A

inferredcites →https://doi.org/10.1038/35059090openalex-snapshot

A sodium-channel mutation causes isolated cardiac conduction disease

inferredcites →https://doi.org/10.1038/376683a0openalex-snapshot

Molecular mechanism for an inherited cardiac arrhythmia

inferredcites →https://doi.org/10.1038/415213aopenalex-snapshot

Cardiac channelopathies

inferredcites →https://doi.org/10.1073/pnas.082121299openalex-snapshot

Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a

inferredcites →https://doi.org/10.1073/pnas.261705699openalex-snapshot

An unexpected role for brain-type sodium channels in coupling of cell surface depolarization to contraction in the heart

inferredcites →https://doi.org/10.1073/pnas.2627986100openalex-snapshot

An unexpected requirement for brain-type sodium channels for control of heart rate in the mouse sinoatrial node

inferredcites →https://doi.org/10.1073/pnas.89.2.554openalex-snapshot

Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel.

inferredcites →https://doi.org/10.1093/hmg/11.3.337openalex-snapshot

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome

inferredcites →https://doi.org/10.1093/hmg/4.9.1603openalex-snapshot

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia

inferredcites →https://doi.org/10.1111/j.1540-8159.1992.tb02960.xopenalex-snapshot

Familial Congenital Sinus Rhythm Anomalies: Clinical and Pathological Correlations

inferredcites →https://doi.org/10.1113/jphysiol.2001.012691openalex-snapshot

The sodium channel -subunit SCN3b modulates the kinetics of SCN5a and is expressed heterogeneously in sheep heart

inferredcites →https://doi.org/10.1136/adc.50.11.879openalex-snapshot

Sick sinus syndrome. Symptomatic cases in children.

inferredcites →https://doi.org/10.1136/adc.51.2.100openalex-snapshot

Sick sinus syndrome in children.

inferredcites →https://doi.org/10.1136/hrt.29.4.469openalex-snapshot

Electrical reversion of cardiac arrhythmias.

inferredcites →https://doi.org/10.1136/hrt.44.6.684openalex-snapshot

Sick sinus syndrome in childhood.

inferredcites →https://doi.org/10.1146/annurev.med.54.073002.182112openalex-snapshot

Genetics and Arrhythmias

inferredcites →https://doi.org/10.1161/01.cir.102.10.1178openalex-snapshot

Spectrum of Mutations in Long-QT Syndrome Genes

inferredcites →https://doi.org/10.1161/01.cir.56.2.235openalex-snapshot

Electrocardiographic recognition of sinus node dysfunction in children and young adults.

inferredcites →https://doi.org/10.1161/01.cir.59.6.1266openalex-snapshot

Sinoatrial conduction in children: an index of sinoatrial node function.

inferredcites →https://doi.org/10.1161/01.cir.68.1.33openalex-snapshot

Persistent sinus nodal electrograms during abnormally prolonged postpacing atrial pauses in sick sinus syndrome in humans: sinoatrial block vs overdrive suppression.

inferredcites →https://doi.org/10.1161/01.res.0000050585.07097.d7openalex-snapshot

A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill

inferredcites →https://doi.org/10.1161/01.res.85.9.803openalex-snapshot

Ionic Mechanisms Responsible for the Electrocardiographic Phenotype of the Brugada Syndrome Are Temperature Dependent

inferredcites →https://doi.org/10.1161/01.res.87.8.e37openalex-snapshot

Enhanced Na + Channel Intermediate Inactivation in Brugada Syndrome

inferredcites →https://doi.org/10.1161/hc0302.102592openalex-snapshot

Clinical, Genetic, and Biophysical Characterization of SCN5A Mutations Associated With Atrioventricular Conduction Block

inferredcites →https://doi.org/10.1161/hc5001.100834openalex-snapshot

NovelSCN5AMutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family

inferredcites →https://doi.org/10.1161/hh1401.095087openalex-snapshot

Homozygous SCN5A Mutation in Long-QT Syndrome With Functional Two-to-One Atrioventricular Block

inferredcites →https://doi.org/10.1172/jci16387openalex-snapshot

Pacemaker channel dysfunction in a patient with sinus node disease

inferredcites →https://doi.org/10.1378/chest.60.3.246openalex-snapshot

Familial Sinus Node Disease

inferredcites →https://doi.org/10.1542/peds.61.4.593openalex-snapshot

Sinus Node Dysfunction in Children, Adolescents, and Young Adults

inferredcites →https://doi.org/10.1542/peds.69.5.590openalex-snapshot

Symptomatic Sinus Node Dysfunction in Children Without Structural Heart Disease

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4640265openalex-extracted

Wnt/β-Catenin Signaling Causes Sinoatrial Node Dysfunction by Inhibition of T-type Calcium Current

inferred← citeshttps://doi.org/10.1001/jama.2013.3219openalex-snapshot

Long QT Syndrome–Associated Mutations in Intrauterine Fetal Death

inferred← citeshttps://doi.org/10.1001/jama.293.4.447openalex-snapshot

Sodium Channel Mutations and Susceptibility to Heart Failure and Atrial Fibrillation

inferred← citeshttps://doi.org/10.1002/9780470015902.a0003634.pub2openalex-snapshot

Brugada Syndrome

inferred← citeshttps://doi.org/10.1002/9780470691977.ch5openalex-snapshot

The Long QT Syndrome

inferred← citeshttps://doi.org/10.1002/9780470750940.refsopenalex-snapshot

References

inferred← citeshttps://doi.org/10.1002/9781119333050.ch3openalex-snapshot

Indications for permanent pacing, device, and lead selection

inferred← citeshttps://doi.org/10.1002/9781119979487.ch30openalex-snapshot

Sinus Node Dysfunction and Sinoatrial Disease

inferred← citeshttps://doi.org/10.1002/acn3.372openalex-snapshot

Biallelic SCN 10A mutations in neuromuscular disease and epileptic encephalopathy

inferred← citeshttps://doi.org/10.1002/ange.202102196openalex-snapshot

Structural Basis for Pore Blockade of the Human Cardiac Sodium Channel Na v 1.5 by the Antiarrhythmic Drug Quinidine**

inferred← citeshttps://doi.org/10.1002/anie.202102196openalex-snapshot

Structural Basis for Pore Blockade of the Human Cardiac Sodium Channel Na v 1.5 by the Antiarrhythmic Drug Quinidine**

inferred← citeshttps://doi.org/10.1002/ar.a.20099openalex-snapshot

Genetics of atrioventricular conduction disease in humans

inferred← citeshttps://doi.org/10.1002/ccr3.1865openalex-snapshot

Pulmonary veins isolation to retard pacemaker implantation

inferred← citeshttps://doi.org/10.1002/cphy.c140069openalex-snapshot

Ion Channels in the Heart

inferred← citeshttps://doi.org/10.1002/humu.21302openalex-snapshot

A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease

inferred← citeshttps://doi.org/10.1002/j.2040-4603.2015.tb00647.xopenalex-snapshot

Ion Channels in the Heart

inferred← citeshttps://doi.org/10.1002/jbt.22993openalex-snapshot

Phenotypes of mutations related to voltage‐dependent sodium channels on children and adolescents

inferred← citeshttps://doi.org/10.1002/joa3.12046openalex-snapshot

Brugada syndrome and sinus node dysfunction

inferred← citeshttps://doi.org/10.1002/joa3.12717openalex-snapshot

European Heart Rhythm Association ( EHRA )/Heart Rhythm Society ( HRS )/Asia Pacific Heart Rhythm Society ( APHRS )/Latin American Heart Rhythm Society ( LAHRS ) Expert Consensus Statement on the state of genetic testing for cardiac diseases

inferred← citeshttps://doi.org/10.1002/joa3.13052openalex-snapshot

JCS / JHRS 2022 Guideline on Diagnosis and Risk Assessment of Arrhythmia

inferred← citeshttps://doi.org/10.1002/joa3.70383openalex-snapshot

Current Topics of Progressive Cardiac Conduction Disease

inferred← citeshttps://doi.org/10.1007/164_2017_43openalex-snapshot

Cardiac Arrhythmias Related to Sodium Channel Dysfunction

inferred← citeshttps://doi.org/10.1007/978-1-4419-6658-2_13openalex-snapshot

Small Animal Models for Arrhythmia Studies

inferred← citeshttps://doi.org/10.1007/978-1-4419-7207-1_18openalex-snapshot

Phenotypic Overlap of Lethal Arrhythmias Associated with Cardiac Sodium Mutations: Individual-Specific or Mutation-Specific?

inferred← citeshttps://doi.org/10.1007/978-1-4419-9461-5_17openalex-snapshot

Dysrhythmias/Channelopathies and Signaling Pathways

inferred← citeshttps://doi.org/10.1007/978-1-4471-4619-3_136openalex-snapshot

Diagnosis of Arrhythmias and Conductive Disorders

inferred← citeshttps://doi.org/10.1007/978-1-4471-4881-4_11openalex-snapshot

Sodium Ion Channelopathies

inferred← citeshttps://doi.org/10.1007/978-1-4471-5316-0_24openalex-snapshot

Cellular Pharmacology of Cardiac Automaticity and Conduction: Implications in Antiarrhythmic Drug Assessment

inferred← citeshttps://doi.org/10.1007/978-1-4471-5316-0_7openalex-snapshot

Understanding the Genetic Basis of Atrial Fibrillation: Towards a Pharmacogenetic Approach for Arrhythmia Treatment

inferred← citeshttps://doi.org/10.1007/978-1-4471-6356-5_12openalex-snapshot

Extracorporeal Life Support

inferred← citeshttps://doi.org/10.1007/978-1-4471-6356-5_27openalex-snapshot

Arrhythmias

inferred← citeshttps://doi.org/10.1007/978-1-4939-2739-5_14openalex-snapshot

Sick Sinus Syndrome

inferred← citeshttps://doi.org/10.1007/978-1-84628-715-2_126openalex-snapshot

Genetic Basis for Cardiac Arrhythmias

inferred← citeshttps://doi.org/10.1007/978-1-84628-854-8_10openalex-snapshot

Sodium Ion Channelopathies

inferred← citeshttps://doi.org/10.1007/978-1-84800-923-3_19openalex-snapshot

Arrhythmias

inferred← citeshttps://doi.org/10.1007/978-1-84996-471-5_13openalex-snapshot

A Molecular Genetic Perspective on Atrial Fibrillation

inferred← citeshttps://doi.org/10.1007/978-3-030-15950-4_32openalex-snapshot

Mass Spectrometry Based Comparative Proteomics Using One Dimensional and Two Dimensional SDS-PAGE of Rat Atria Induced with Obstructive Sleep Apnea

inferred← citeshttps://doi.org/10.1007/978-3-030-35374-2_20openalex-snapshot

Specific Cardiovascular Diseases and Competitive Sports Participation: Channelopathies

inferred← citeshttps://doi.org/10.1007/978-3-030-45457-9_18openalex-snapshot

A Molecular Genetic Perspective on Atrial Fibrillation

inferred← citeshttps://doi.org/10.1007/978-3-031-32625-7_6openalex-snapshot

Antepartum Noninvasive Evaluation of Fetal Myocardial Performance from Continuous Doppler Signals and Its Research Potential

inferred← citeshttps://doi.org/10.1007/978-3-031-33588-4_27openalex-snapshot

Defects in Ankyrin-based Protein Targeting Pathways in Human Arrhythmia

inferred← citeshttps://doi.org/10.1007/978-3-031-33588-4_6openalex-snapshot

Unique Features of the Human Sinoatrial Node Structure, Function, and Arrhythmias: Mechanistic Insights from Integrated 3D Mapping Approaches

inferred← citeshttps://doi.org/10.1007/978-3-319-09102-0_15openalex-snapshot

Differential Diagnosis of Vasovagal Syncope: Sick Sinus Syndrome

inferred← citeshttps://doi.org/10.1007/978-3-319-44203-7_11openalex-snapshot

Brugada Syndrome

inferred← citeshttps://doi.org/10.1007/978-3-319-44203-7_15openalex-snapshot

A Molecular Genetic Perspective on Atrial Fibrillation

inferred← citeshttps://doi.org/10.1007/978-3-319-66114-8_14openalex-snapshot

Inherited Arrhythmias: Brugada Syndrome and Early Repolarisation Syndrome

inferred← citeshttps://doi.org/10.1007/978-3-319-66114-8_15openalex-snapshot

Inherited Conduction Disease and Atrial Fibrillation

inferred← citeshttps://doi.org/10.1007/978-3-319-66816-1_1277-1openalex-snapshot

Sick Sinus Syndrome (SSS): Types 1–3

inferred← citeshttps://doi.org/10.1007/978-3-319-66816-1_1278-1openalex-snapshot

Sick Sinus Syndrome and Myopia

inferred← citeshttps://doi.org/10.1007/978-3-319-77812-9_2openalex-snapshot

Cardiac Sodium Channel (Dys)Function and Inherited Arrhythmia Syndromes

inferred← citeshttps://doi.org/10.1007/978-3-319-77812-9_8openalex-snapshot

Brugada Syndrome: Current Perspectives

inferred← citeshttps://doi.org/10.1007/978-3-319-77812-9_9openalex-snapshot

Sinus Node Disease and Cardiac Conduction Disease

inferred← citeshttps://doi.org/10.1007/978-3-540-72110-9_8openalex-snapshot

Propagation of Pacemaker Activity

inferred← citeshttps://doi.org/10.1007/978-3-642-17575-6_22openalex-snapshot

Molecular Mechanisms of Voltage-Gated Na+ Channel Dysfunction in LQT3 Syndrome

inferred← citeshttps://doi.org/10.1007/978-3-642-17575-6_25openalex-snapshot

Defects in Ankyrin-Based Protein Targeting Pathways in Human Arrhythmia

inferred← citeshttps://doi.org/10.1007/978-981-96-7667-5_3openalex-snapshot

Bradyarrhythmias

inferred← citeshttps://doi.org/10.1007/bf03085988openalex-snapshot

Diversity in cardiac sodium channel disease phenotype in transgenic mice carrying a single SCN5A mutation

inferred← citeshttps://doi.org/10.1007/s00018-016-2400-1openalex-snapshot

Development of the cardiac pacemaker

inferred← citeshttps://doi.org/10.1007/s00109-018-1685-yopenalex-snapshot

Translating emerging molecular genetic insights into clinical practice in inherited cardiomyopathies

inferred← citeshttps://doi.org/10.1007/s00246-012-0303-yopenalex-snapshot

Cardiac Sodium Channel Nav1.5 Mutations and Cardiac Arrhythmia

inferred← citeshttps://doi.org/10.1007/s00246-013-0773-6openalex-snapshot

The SCN5A Mutation A1180V is Associated With Electrocardiographic Features of LQT3

inferred← citeshttps://doi.org/10.1007/s00395-009-0012-8openalex-snapshot

The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium

inferred← citeshttps://doi.org/10.1007/s00395-014-0446-5openalex-snapshot

Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations

inferred← citeshttps://doi.org/10.1007/s00395-015-0468-7openalex-snapshot

Loss of dihydrolipoyl succinyltransferase (DLST) leads to reduced resting heart rate in the zebrafish

inferred← citeshttps://doi.org/10.1007/s00399-007-0564-yopenalex-snapshot

Stroke complicating congenital sick sinus syndrome

inferred← citeshttps://doi.org/10.1007/s00414-026-03720-5openalex-snapshot

SCN5A c.4720G> A: a rare genetic variant associated with familial sick sinus syndrome and sudden cardiac death

inferred← citeshttps://doi.org/10.1007/s00424-007-0216-4openalex-snapshot

Downregulation of neuronal sodium channel subunits Nav1.1 and Nav1.6 in the sinoatrial node from volume-overloaded heart failure rat

inferred← citeshttps://doi.org/10.1007/s00424-009-0761-0openalex-snapshot

Cardiac sodium channelopathies

inferred← citeshttps://doi.org/10.1007/s00424-023-02882-0openalex-snapshot

GPD1L-A306del modifies sodium current in a family carrying the dysfunctional SCN5A-G1661R mutation associated with Brugada syndrome

inferred← citeshttps://doi.org/10.1007/s10330-016-0232-2openalex-snapshot

Retroperitoneal hyaline-vascular variant Castleman Disease in a patient with iron-deficiency anemia and sinus bradycardia: a case report

inferred← citeshttps://doi.org/10.1007/s10840-015-9998-zopenalex-snapshot

The genetic basis for inherited forms of sinoatrial dysfunction and atrioventricular node dysfunction

inferred← citeshttps://doi.org/10.1007/s11427-013-4533-xopenalex-snapshot

Effects of external stimuli on the pacemaker function of the sinoatrial node in sodium channel gene mutations models

inferred← citeshttps://doi.org/10.1007/s11517-006-0102-9openalex-snapshot

Propagation of pacemaker activity

inferred← citeshttps://doi.org/10.1007/s11568-009-9027-3openalex-snapshot

In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs)

inferred← citeshttps://doi.org/10.1007/s12041-018-0902-3openalex-snapshot

Development and diversity of a novel panel of short tandem repeat markers encompassing the SCN5A gene in Iranian population

inferred← citeshttps://doi.org/10.1016/b978-0-12-369420-1.00062-7openalex-snapshot

Genetics and Genomics of Arrhythmias

inferred← citeshttps://doi.org/10.1016/b978-0-12-374934-5.00029-5openalex-snapshot

Genetics and Genomics of Arrhythmias

inferred← citeshttps://doi.org/10.1016/b978-0-12-381510-1.00042-9openalex-snapshot

Genetic Mechanisms of Arrhythmia

inferred← citeshttps://doi.org/10.1016/b978-0-12-383834-6.00057-4openalex-snapshot

The Genetics of Cardiac Electrophysiology in Humans

inferred← citeshttps://doi.org/10.1016/b978-0-12-404599-6.00017-2openalex-snapshot

Post-Genomic Analysis of Dysrhythmias and Sudden Death

inferred← citeshttps://doi.org/10.1016/b978-0-12-405206-2.00007-7openalex-snapshot

Cellular and Molecular Pathobiology of the Cardiac Conduction System

inferred← citeshttps://doi.org/10.1016/b978-0-12-417197-8.00012-2openalex-snapshot

Sodium Channels, Cardiac Arrhythmia, and Therapeutic Strategy

inferred← citeshttps://doi.org/10.1016/b978-0-12-420014-2.00009-0openalex-snapshot

Sick Sinus Syndrome

inferred← citeshttps://doi.org/10.1016/b978-0-12-812532-8.00004-5openalex-snapshot

Genetics of Electrophysiologic Disorders

inferred← citeshttps://doi.org/10.1016/b978-0-12-813704-8.00036-xopenalex-snapshot

Molecular therapies for bradyarrhythmias

inferred← citeshttps://doi.org/10.1016/b978-0-12-817728-0.00063-2openalex-snapshot

Pregnancy in Congenital Long QT and Brugada syndrome patients

inferred← citeshttps://doi.org/10.1016/b978-0-12-823882-0.00002-3openalex-snapshot

Induced pluripotent stem cells for modeling cardiac sodium channelopathies

inferred← citeshttps://doi.org/10.1016/b978-0-323-07307-3.10028-xopenalex-snapshot

Disorders of Cardiac Rhythm

inferred← citeshttps://doi.org/10.1016/b978-0-323-37804-8.00019-5openalex-snapshot

Pacing and Defibrillation Use in Pediatric Patients

inferred← citeshttps://doi.org/10.1016/b978-0-323-44733-1.00028-6openalex-snapshot

Mechanisms of Normal and Dysfunctional Sinoatrial Nodal Excitability and Propagation

inferred← citeshttps://doi.org/10.1016/b978-0-323-44733-1.00050-xopenalex-snapshot

Mechanisms in Heritable Sodium Channel Diseases

inferred← citeshttps://doi.org/10.1016/b978-0-323-44733-1.00072-9openalex-snapshot

Sinus Node Abnormalities

inferred← citeshttps://doi.org/10.1016/b978-0-323-44733-1.00092-4openalex-snapshot

Brugada Syndrome

inferred← citeshttps://doi.org/10.1016/b978-0-323-44733-1.00105-xopenalex-snapshot

Progressive Conduction System Disease

inferred← citeshttps://doi.org/10.1016/b978-0-323-44733-1.00109-7openalex-snapshot

Arrhythmias in the Pediatric Population

inferred← citeshttps://doi.org/10.1016/b978-0-323-99570-2.00006-0openalex-snapshot

Composition and function of ion channels and their effects on cardiac remodeling

inferred← citeshttps://doi.org/10.1016/b978-012373698-7/50017-6openalex-snapshot

Dysrhythmias and Sudden Death

inferred← citeshttps://doi.org/10.1016/b978-032301808-1.50029-8openalex-snapshot

Disorders of Cardiac Rhythm

inferred← citeshttps://doi.org/10.1016/b978-1-4160-2536-8.50018-2openalex-snapshot

Pacing for Sinus Node Disease: Indications, Techniques, and Clinical Trials

inferred← citeshttps://doi.org/10.1016/b978-1-4377-0285-9.00076-4openalex-snapshot

Assessment and Treatment of Fetal Arrhythmias

inferred← citeshttps://doi.org/10.1016/b978-1-4377-0285-9.00079-xopenalex-snapshot

Pacemaker and Implantable Cardioverter-Defibrillator Therapy in Pediatric Patients with and Without Congenital Heart Disease

inferred← citeshttps://doi.org/10.1016/b978-1-4377-0398-6.00009-3openalex-snapshot

Genetics of Cardiac Arrhythmias

inferred← citeshttps://doi.org/10.1016/b978-1-4377-1616-0.00013-8openalex-snapshot

Pacing for Sinus Node Disease

inferred← citeshttps://doi.org/10.1016/b978-1-4557-2856-5.00050-9openalex-snapshot

Mechanisms in Heritable Sodium Channel Diseases

inferred← citeshttps://doi.org/10.1016/b978-1-4557-2856-5.00072-8openalex-snapshot

Sinus Node Abnormalities

inferred← citeshttps://doi.org/10.1016/b978-1-4557-2856-5.00092-3openalex-snapshot

Brugada Syndrome 1992–2012

inferred← citeshttps://doi.org/10.1016/b978-1-4557-2856-5.00105-9openalex-snapshot

Progressive Conduction System Disease

inferred← citeshttps://doi.org/10.1016/b978-141603774-3.10031-0openalex-snapshot

Cardiac Arrhythmias in the Fetus, Infants, Children, and Adolescents with Congenital Heart Disease

inferred← citeshttps://doi.org/10.1016/b978-84-8086-956-0.00009-5openalex-snapshot

10.1016/b978-84-8086-956-0.00009-5

inferred← citeshttps://doi.org/10.1016/bs.ctdb.2024.02.006openalex-snapshot

The cardiac conduction system: History, development, and disease

inferred← citeshttps://doi.org/10.1016/j.ajhg.2020.05.015openalex-snapshot

High-Throughput Reclassification of SCN5A Variants

inferred← citeshttps://doi.org/10.1016/j.bbapap.2015.07.009openalex-snapshot

The multi-faceted aspects of the complex cardiac Nav1.5 protein in membrane function and pathophysiology

inferred← citeshttps://doi.org/10.1016/j.bcp.2022.115206openalex-snapshot

Regulation of cardiac ion channels by transcription factors: Looking for new opportunities of druggable targets for the treatment of arrhythmias

inferred← citeshttps://doi.org/10.1016/j.biopha.2026.119386openalex-snapshot

Beta-cardiotoxin, a funny current inhibitor, and its effect on ion channels involved in heart rate regulation and on calcium transient profile in mouse sinoatrial node cells

inferred← citeshttps://doi.org/10.1016/j.bmcl.2021.128133openalex-snapshot

Identification of aryl sulfonamides as novel and potent inhibitors of NaV1.5

inferred← citeshttps://doi.org/10.1016/j.bpj.2016.02.010openalex-snapshot

Inherited Arrhythmias: Of Channels, Currents, and Swimming

inferred← citeshttps://doi.org/10.1016/j.bpj.2024.04.017openalex-snapshot

Conformational photo-trapping in NaV1.5: Inferring local motions at the “inactivation gate”

inferred← citeshttps://doi.org/10.1016/j.cardiores.2007.01.009openalex-snapshot

SCN5A and sinoatrial node pacemaker function

inferred← citeshttps://doi.org/10.1016/j.cardiores.2007.08.006openalex-snapshot

A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia

inferred← citeshttps://doi.org/10.1016/j.ccell.2008.01.008openalex-snapshot

Congenital Heart Disease and Genetics

inferred← citeshttps://doi.org/10.1016/j.ccep.2010.09.001openalex-snapshot

Genetics of Sick Sinus Syndrome

inferred← citeshttps://doi.org/10.1016/j.ccep.2010.09.007openalex-snapshot

Progressive Conduction Diseases

inferred← citeshttps://doi.org/10.1016/j.ccep.2010.10.004openalex-snapshot

Inherited Cardiac Arrhythmia Syndromes: Role of the Sodium Channel

inferred← citeshttps://doi.org/10.1016/j.ccep.2014.07.001openalex-snapshot

Role of Rare and Common Genetic Variation in SCN5A in Cardiac Electrical Function and Arrhythmia

inferred← citeshttps://doi.org/10.1016/j.ccep.2014.08.002openalex-snapshot

Sodium Current Disorders

inferred← citeshttps://doi.org/10.1016/j.ccep.2014.08.003openalex-snapshot

Sodium Current Disorders

inferred← citeshttps://doi.org/10.1016/j.ccep.2014.08.005openalex-snapshot

Cardiac Sodium Channel Overlap Syndrome

inferred← citeshttps://doi.org/10.1016/j.ccep.2018.02.002openalex-snapshot

Sick Sinus Syndrome

inferred← citeshttps://doi.org/10.1016/j.ccep.2021.06.005openalex-snapshot

Genetic Abnormalities of the Sinoatrial Node and Atrioventricular Conduction

inferred← citeshttps://doi.org/10.1016/j.ccep.2021.06.006openalex-snapshot

Sinus Node Dysfunction

inferred← citeshttps://doi.org/10.1016/j.ccl.2023.03.013openalex-snapshot

Sinus Node Dysfunction

inferred← citeshttps://doi.org/10.1016/j.ccl.2023.03.014openalex-snapshot

Genetic Abnormalities of the Sinoatrial Node and Atrioventricular Conduction

inferred← citeshttps://doi.org/10.1016/j.cpcardiol.2019.100454openalex-snapshot

Update on Brugada Syndrome 2019

inferred← citeshttps://doi.org/10.1016/j.crphys.2021.02.002openalex-snapshot

Investigating myocardial performance in normal and sick fetuses by abdominal Doppler signal derived indices

inferred← citeshttps://doi.org/10.1016/j.disamonth.2023.101637openalex-snapshot

Tachy-brady syndrome: Electrophysiology and evolving principles of management

inferred← citeshttps://doi.org/10.1016/j.ejphar.2005.11.035openalex-snapshot

Pharmacological characterisation of sodium channels in sinoatrial node pacemaking in the rat heart

inferred← citeshttps://doi.org/10.1016/j.ejphar.2015.02.019openalex-snapshot

The effects of A-803467 on cardiac Nav1.5 channels

inferred← citeshttps://doi.org/10.1016/j.forsciint.2008.09.013openalex-snapshot

Molecular genetics of sudden cardiac death

inferred← citeshttps://doi.org/10.1016/j.forsciint.2017.02.038openalex-snapshot

Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene

inferred← citeshttps://doi.org/10.1016/j.fsigen.2025.103237openalex-snapshot

SCN5A missense variants and their contribution to deaths in Sudden Unexplained Nocturnal Death Syndrome (SUNDS)

inferred← citeshttps://doi.org/10.1016/j.gde.2007.04.010openalex-snapshot

Genetic determinants of QT interval variation and sudden cardiac death

inferred← citeshttps://doi.org/10.1016/j.gene.2015.08.062openalex-snapshot

The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology

inferred← citeshttps://doi.org/10.1016/j.gene.2019.143990openalex-snapshot

A newly identified missense mutation in CLCA2 is associated with autosomal dominant cardiac conduction block

inferred← citeshttps://doi.org/10.1016/j.genhosppsych.2014.07.001openalex-snapshot

Electrocardiography changes in bipolar patients during long-term lithium monotherapy

inferred← citeshttps://doi.org/10.1016/j.hrcr.2018.04.015openalex-snapshot

Long-term follow-up of permanent atrial standstill in a German family with mutation in the SCN5A gene

inferred← citeshttps://doi.org/10.1016/j.hrcr.2020.11.016openalex-snapshot

Familial sick sinus syndrome possibly associated with novel SCN5A mutation diagnosed in pregnancy

inferred← citeshttps://doi.org/10.1016/j.hrcr.2021.08.013openalex-snapshot

Incessant atrial and ventricular tachycardias associated with an SCN5A mutation

inferred← citeshttps://doi.org/10.1016/j.hrcr.2023.06.017openalex-snapshot

A novel association between sinus node dysfunction and an SCN5A variant presenting as persistent symptomatic bradycardia in a young adult

inferred← citeshttps://doi.org/10.1016/j.hroo.2025.06.010openalex-snapshot

Clinical presentation and outcomes of patients with biallelic SCN5A variants: A systematic review

inferred← citeshttps://doi.org/10.1016/j.hrthm.2005.01.029openalex-snapshot

Novel Brugada SCN5A mutation causing sudden death in children

inferred← citeshttps://doi.org/10.1016/j.hrthm.2005.06.032openalex-snapshot

Congenital atrial standstill associated with coinheritance of a novel SCN5A mutation and connexin 40 polymorphisms

inferred← citeshttps://doi.org/10.1016/j.hrthm.2007.06.022openalex-snapshot

Long QT and Brugada syndrome gene mutations in New Zealand

inferred← citeshttps://doi.org/10.1016/j.hrthm.2007.09.015openalex-snapshot

Cardiac sodium channel mutation in atrial fibrillation

inferred← citeshttps://doi.org/10.1016/j.hrthm.2008.01.039openalex-snapshot

Polymorphisms in multiple genes are associated with resting heart rate in a stepwise allele-dependent manner

inferred← citeshttps://doi.org/10.1016/j.hrthm.2008.04.014openalex-snapshot

ACC/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities

inferred← citeshttps://doi.org/10.1016/j.hrthm.2009.02.022openalex-snapshot

Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae

inferred← citeshttps://doi.org/10.1016/j.hrthm.2009.04.026openalex-snapshot

Atrial standstill associated with loss of atrial myocytes: A rare cause of fetal bradyarrhythmia

inferred← citeshttps://doi.org/10.1016/j.hrthm.2009.04.034openalex-snapshot

Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A

inferred← citeshttps://doi.org/10.1016/j.hrthm.2009.05.012openalex-snapshot

Compound heterozygous SCN5A mutations: Does the sum of the parts equal the whole?

inferred← citeshttps://doi.org/10.1016/j.hrthm.2010.10.014openalex-snapshot

Homozygous mutation in SCN5A associated with atrial quiescence, recalcitrant arrhythmias, and poor capture thresholds

inferred← citeshttps://doi.org/10.1016/j.hrthm.2011.05.020openalex-snapshot

HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies

inferred← citeshttps://doi.org/10.1016/j.hrthm.2011.06.029openalex-snapshot

Relative contribution of changes in sodium current versus intercellular coupling on reentry initiation in 2-dimensional preparations of plakophilin-2–deficient cardiac cells

inferred← citeshttps://doi.org/10.1016/j.hrthm.2012.02.023openalex-snapshot

Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation

inferred← citeshttps://doi.org/10.1016/j.hrthm.2012.08.033openalex-snapshot

Phenotype, genotype, and cellular physiology: Need for clarity in characterization

inferred← citeshttps://doi.org/10.1016/j.hrthm.2013.09.060openalex-snapshot

Life-threatening ventricular arrhythmias during ajmaline challenge in patients with Brugada syndrome: Incidence, clinical features, and prognosis

inferred← citeshttps://doi.org/10.1016/j.hrthm.2014.04.026openalex-snapshot

Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation

inferred← citeshttps://doi.org/10.1016/j.hrthm.2015.05.032openalex-snapshot

Enhanced fast-inactivated state stability of cardiac sodium channels by a novel voltage sensor SCN5A mutation, R1632C, as a cause of atypical Brugada syndrome

inferred← citeshttps://doi.org/10.1016/j.hrthm.2015.08.021openalex-snapshot

Cardiac sodium channel mutation associated with epinephrine-induced QT prolongation and sinus node dysfunction

inferred← citeshttps://doi.org/10.1016/j.hrthm.2017.01.020openalex-snapshot

Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction

inferred← citeshttps://doi.org/10.1016/j.hrthm.2022.01.034openalex-snapshot

SCN5A mutation in Brugada syndrome is associated with substrate severity detected by electrocardiographic imaging and high-density electroanatomic mapping

inferred← citeshttps://doi.org/10.1016/j.hrthm.2022.03.1223openalex-snapshot

SCN5A overlap syndromes: An open-minded approach

inferred← citeshttps://doi.org/10.1016/j.hrthm.2022.03.1225openalex-snapshot

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases

inferred← citeshttps://doi.org/10.1016/j.hrthm.2024.08.018openalex-snapshot

Systematic analysis of SCN5A variants associated with inherited cardiac diseases

inferred← citeshttps://doi.org/10.1016/j.ijcard.2012.08.032openalex-snapshot

Novel deletion mutation in the cardiac sodium channel inactivation gate causes long QT syndrome

inferred← citeshttps://doi.org/10.1016/j.ijcard.2012.11.062openalex-snapshot

Autosomal recessive paediatric sick sinus syndrome associated with novel compound mutations in SCN5A

inferred← citeshttps://doi.org/10.1016/j.ijcard.2013.11.013openalex-snapshot

Genetic analysis in a family affected by sick sinus syndrome may reduce the sudden death risk in a young aspiring competitive athlete

inferred← citeshttps://doi.org/10.1016/j.ijcard.2016.01.160openalex-snapshot

Autosomal recessive atrial disease presenting with sick sinus syndrome (SSS), right atrial fibrosis and biatrial dilatation: Clinical impact of genetic diagnosis

inferred← citeshttps://doi.org/10.1016/j.ijcard.2017.01.113openalex-snapshot

Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillation

inferred← citeshttps://doi.org/10.1016/j.ijcard.2022.05.071openalex-snapshot

Molecular genetic testing in athletes: Why and when a position statement from the Italian Society of Sports Cardiology

inferred← citeshttps://doi.org/10.1016/j.ijcard.2024.132609openalex-snapshot

Genetic basis and causal relationship between atrial fibrillation and sinus node dysfunction: Evidence from comprehensive genetic analysis

inferred← citeshttps://doi.org/10.1016/j.ijcha.2015.10.003openalex-snapshot

Conduction abnormalities and ventricular arrhythmogenesis: The roles of sodium channels and gap junctions

inferred← citeshttps://doi.org/10.1016/j.ijcha.2020.100468openalex-snapshot

Brugada syndrome: A comprehensive review of pathophysiological mechanisms and risk stratification strategies

inferred← citeshttps://doi.org/10.1016/j.isci.2024.109696openalex-snapshot

Popeye domain containing proteins modulate the voltage-gated cardiac sodium channel Nav1.5

inferred← citeshttps://doi.org/10.1016/j.jacc.2005.02.014openalex-snapshot

Task Force 7: Arrhythmias

inferred← citeshttps://doi.org/10.1016/j.jacc.2005.08.043openalex-snapshot

High Risk for Bradyarrhythmic Complications in Patients With Brugada Syndrome Caused by SCN5AGene Mutations

inferred← citeshttps://doi.org/10.1016/j.jacc.2007.10.060openalex-snapshot

Atrial Fibrillation in Patients With Brugada Syndrome

inferred← citeshttps://doi.org/10.1016/j.jacc.2008.02.032openalex-snapshot

ACC/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities

inferred← citeshttps://doi.org/10.1016/j.jacc.2008.07.013openalex-snapshot

A Novel SCN5A Gain-of-Function Mutation M1875T Associated With Familial Atrial Fibrillation

inferred← citeshttps://doi.org/10.1016/j.jacc.2009.12.005openalex-snapshot

Impact of Genetic Discoveries on the Classification of Lone Atrial Fibrillation

inferred← citeshttps://doi.org/10.1016/j.jacc.2012.11.007openalex-snapshot

2012 ACCF/AHA/HRS Focused Update Incorporated Into the ACCF/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities

inferred← citeshttps://doi.org/10.1016/j.jacc.2013.04.041openalex-snapshot

Provocation of an Autoimmune Response to Cardiac Voltage-Gated Sodium Channel NaV1.5 Induces Cardiac Conduction Defects in Rats

inferred← citeshttps://doi.org/10.1016/j.jacc.2014.05.045openalex-snapshot

HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy

inferred← citeshttps://doi.org/10.1016/j.jacep.2018.03.006openalex-snapshot

Clinical Spectrum of SCN5A Mutations

inferred← citeshttps://doi.org/10.1016/j.jacep.2022.08.003openalex-snapshot

Molecular and Functional Remodeling of Superior and Inferior SAN in a Rat Model of HCM

inferred← citeshttps://doi.org/10.1016/j.jacep.2022.08.022openalex-snapshot

Atrial Standstill in the Pediatric Population

inferred← citeshttps://doi.org/10.1016/j.jacep.2022.11.025openalex-snapshot

Time to Move Forward on Pediatric Atrial Standstill

inferred← citeshttps://doi.org/10.1016/j.jelectrocard.2004.08.002openalex-snapshot

Molecular basis of congenital and acquired long QT syndromes

inferred← citeshttps://doi.org/10.1016/j.jelectrocard.2007.05.033openalex-snapshot

Genetic mutations and arrhythmia: simulation from DNA to electrocardiogram

inferred← citeshttps://doi.org/10.1016/j.jelectrocard.2021.01.019openalex-snapshot

Multiple arrhythmic and cardiomyopathic phenotypes associated with an SCN5A A735E mutation

inferred← citeshttps://doi.org/10.1016/j.jjcc.2012.12.006openalex-snapshot

Sinus node disease in subjects with type 1 ECG pattern of Brugada syndrome

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