(Q33156246)

English

Subepicardial phase 0 block and discontinuous transmural conduction underlie right precordial ST-segment elevation by a SCN5A loss-of-function mutation.

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scholarly article

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6 January 2020

Subepicardial phase 0 block and discontinuous transmural conduction underlie right precordial ST-segment elevation by a SCN5A loss-of-function mutation (English)

1 reference

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6 January 2020

2

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6 January 2020

author name string

Markéta Bébarová

1

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6 January 2020

Jan L M C Geelen

3

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6 January 2020

Roselie J Jongbloed

4

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6 January 2020

Carl Timmermans

5

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6 January 2020

Yvonne H Arens

6

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6 January 2020

Luz-Maria Rodriguez

7

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6 January 2020

Yoram Rudy

8

1 reference

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6 January 2020

Paul G A Volders

9

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6 January 2020

publication date

2 May 2008

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6 January 2020

American Journal of Physiology Heart and Circulatory Physiology

1 reference

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6 January 2020

295

1 reference

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6 January 2020

H48-58

1 reference

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6 January 2020

1

1 reference

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6 January 2020

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Cardiac histological substrate in patients with clinical phenotype of Brugada syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Pathophysiological mechanisms of Brugada syndrome: depolarization disorder, repolarization disorder, or more?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Unconventional intronic splice site mutation in SCN5A associates with cardiac sodium channelopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Ionic current basis of electrocardiographic waveforms: a model study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Na(+) channel mutation that causes both Brugada and long-QT syndrome phenotypes: a simulation study of mechanism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Role of the C-terminal domain in inactivation of brain and cardiac sodium channels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Action potential and contractility changes in [Na(+)](i) overloaded cardiac myocytes: a simulation study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Temperature dependence of early and late currents in human cardiac wild-type and long Q-T DeltaKPQ Na+ channels.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Modulating L-type calcium current affects discontinuous cardiac action potential conduction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Transient outward current prominent in canine ventricular epicardium but not endocardium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Heterogeneity within the ventricular wall. Electrophysiology and pharmacology of epicardial, endocardial, and M cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

21 June 2018

Cardiac sodium channel gene variants and sudden cardiac death in women.

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.91495.2007

21 January 2018

Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction.

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.91495.2007

21 January 2018

The circadian pattern of the development of ventricular fibrillation in patients with Brugada syndrome.

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.91495.2007

21 January 2018

Vagal activity modulates spontaneous augmentation of ST elevation in the daily life of patients with Brugada syndrome.

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.91495.2007

21 January 2018

Cardiac sodium channel dysfunction in sudden infant death syndrome.

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.91495.2007

21 January 2018

Electrical heterogeneity of canine right ventricular transient outward potassium currents

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

31 October 2018

Transmural heterogeneity of action potentials and Ito1 in myocytes isolated from the human right ventricle.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494753

31 October 2018

Linking a genetic defect to its cellular phenotype in a cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.91495.2007

21 January 2018

Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Secondary structure of the human cardiac Na+ channel C terminus: evidence for a role of helical structures in modulation of channel inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late potentials and the Brugada syndrome**Editorials published in the Journal of the American College of Cardiologyreflect the views of the authors and do not necessarily represent the views of JACCor the American College of Cardiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transmural action potential and ionic current remodeling in ventricles of failing canine hearts

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ionic bases for electrophysiological distinctions among epicardial, midmyocardial, and endocardial myocytes from the free wall of the canine left ventricle

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Recurrent ventricular fibrillation, right bundle-branch block and persistent ST segment elevation in V1-V3: a new arrhythmia syndrome? A clinical case report]

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Physiology and pathophysiology of cardiac impulse conduction]

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Idiopathic ventricular fibrillation induced with vagal activity in patients without obvious heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ionic mechanisms of propagation in cardiac tissue. Roles of the sodium and L-type calcium currents during reduced excitability and decreased gap junction coupling

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Slow conduction in cardiac tissue, II: effects of branching tissue geometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of IKr and IKs heterogeneity on action potential duration and its rate dependence: a simulation study

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cryptic 5' splice site activation in SCN5A associated with Brugada syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Action potential propagation in inhomogeneous cardiac tissue: safety factor considerations and ionic mechanism

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two distinct congenital arrhythmias evoked by a multidysfunctional Na(+) channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/18456723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1152/AJPHEART.91495.2007

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18456723%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18456723%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18456723%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

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