Subepicardial phase 0 block and discontinuous transmural conduction underlie right precordial ST-segment elevation by a SCN5A loss-of-function mutation. (Q33156246)

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

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6 January 2020

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6 January 2020

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Markéta Bébarová

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6 January 2020

Jan L M C Geelen

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6 January 2020

Roselie J Jongbloed

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6 January 2020

Carl Timmermans

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6 January 2020

Yvonne H Arens

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6 January 2020

Luz-Maria Rodriguez

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6 January 2020

Yoram Rudy

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6 January 2020

Paul G A Volders

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2 May 2008

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6 January 2020

American Journal of Physiology Heart and Circulatory Physiology

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6 January 2020

295

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6 January 2020

1

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6 January 2020

H48-58

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6 January 2020

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21 June 2018

Cardiac histological substrate in patients with clinical phenotype of Brugada syndrome

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

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21 June 2018

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

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21 June 2018

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

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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

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21 June 2018

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

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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

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21 June 2018

Ionic current basis of electrocardiographic waveforms: a model study

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21 June 2018

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

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21 June 2018

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

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21 June 2018

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

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21 June 2018

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

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21 June 2018

Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes

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21 June 2018

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

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21 June 2018

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

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21 June 2018

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

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21 June 2018

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

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21 June 2018

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

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21 June 2018

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

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21 June 2018

Transient outward current prominent in canine ventricular epicardium but not endocardium

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21 June 2018

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

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21 June 2018

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21 June 2018

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

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

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

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

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Cardiac sodium channel dysfunction in sudden infant death syndrome.

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Electrical heterogeneity of canine right ventricular transient outward potassium currents

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31 October 2018

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

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31 October 2018

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

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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

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12 December 2020

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

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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

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

12 December 2020

based on heuristic

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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

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

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

12 December 2020

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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

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

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

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[Physiology and pathophysiology of cardiac impulse conduction]

1 reference

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

12 December 2020

based on heuristic

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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

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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

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based on heuristic

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1 reference

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

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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

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

1 reference

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Identifiers

10.1152/AJPHEART.91495.2007

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6 January 2020

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6 January 2020

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6 January 2020

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