Cardiac Sodium Channel Diseases (Q35127761)

6 August 2017

1 reference

title

Cardiac sodium channel diseases (English)

1 reference

6 August 2017

Cardiac Sodium Channel Diseases (English)

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

2 January 2024

1

Carlo Napolitano

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12747584

2 January 2024

author name string

Ilaria Rivolta

2

1 reference

6 August 2017

Silvia G. Priori

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12747584

2 January 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12747584

2 January 2024

publication date

1 April 2003

1 reference

full work available at URL

6 August 2017

https://www.degruyter.com/document/doi/10.1515/CCLM.2003.066/pdf

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

Clinical Chemistry and Laboratory Medicine

2 January 2024

published in

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6 August 2017

volume

41

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6 August 2017

issue

4

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6 August 2017

page(s)

439-444

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

6 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Cardiac conduction defects associate with mutations in SCN5A

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Molecular mechanism for an inherited cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

De novo mutation in the SCN5A gene associated with early onset of sudden infant death

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

A mutant cardiac sodium channel with multiple biophysical defects associated with overlapping clinical features of Brugada syndrome and cardiac conduction disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Three-year follow-up of patients with right bundle branch block and ST segment elevation in the right precordial leads: Japanese Registry of Brugada Syndrome. Idiopathic Ventricular Fibrillation Investigators

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Relatively benign clinical course in asymptomatic patients with brugada-type electrocardiogram without family history of sudden death

21 January 2018

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https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G).

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

ETIOLOGY AND PATHOLOGY OF BILATERAL BUNDLE BRANCH BLOCK IN RELATION TO COMPLETE HEART BLOCK.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

A sodium-channel mutation causes isolated cardiac conduction disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Autonomic and antiarrhythmic drug modulation of ST segment elevation in patients with Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Foretelling the future in Brugada syndrome: do we have the crystal ball?

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.066

Novel LQT-3 mutation affects Na+ channel activity through interactions between alpha- and beta1-subunits

21 January 2018

7

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

Modulation of cardiac Na+ current phenotype by beta1-subunit expression

2 January 2024

8

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

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

2 January 2024

9

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

Sodium channel abnormalities are infrequent in patients with long QT syndrome: identification of two novel SCN5A mutations

2 January 2024

12

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

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

2 January 2024

13

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

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

2 January 2024

16

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families

2 January 2024

21

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

Right bundle-branch block and ST-segment elevation in leads V1 through V3: a marker for sudden death in patients without demonstrable structural heart disease

2 January 2024

24

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

Enhanced Na(+) channel intermediate inactivation in Brugada syndrome

2 January 2024

27

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

Accelerated inactivation in a mutant Na(+) channel associated with idiopathic ventricular fibrillation

2 January 2024

29

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

The Pathogenesis of Atrioventricular Block in Coronary Disease

2 January 2024

32

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

Defective cardiac ion channels: from mutations to clinical syndromes

2 January 2024

34

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

2 January 2024

36

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

2 January 2024

37

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

Cellular basis for the Brugada syndrome and other mechanisms of arrhythmogenesis associated with ST-segment elevation

2 January 2024

39

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation

2 January 2024

40

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

The Elusive Link Between LQT3 and Brugada Syndrome

2 January 2024

43

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation

2 January 2024

45

1 reference

https://api.crossref.org/works/10.1515/CCLM.2003.066

2 January 2024

Identifiers

1 reference

6 August 2017

1 reference