(Q36724804)

English

Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome

scientific article published on 16 February 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome (English)

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Michael J Ackerman

3

object named as

Michael J Ackerman

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

author name string

David W Van Norstrand

1

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

David J Tester

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

publication date

16 February 2008

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

5

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

5

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

712-715

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

30 September 2017

Infant mortality statistics from the 2004 period linked birth/infant death data set.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

30 September 2017

A mechanism for sudden infant death syndrome (SIDS): stress-induced leak via ryanodine receptors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

30 September 2017

Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

30 September 2017

Prevalence of long-QT syndrome gene variants in sudden infant death syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

30 September 2017

A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

30 September 2017

Sudden infant death syndrome: how significant are the cardiac channelopathies?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

30 September 2017

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

30 September 2017

A molecular link between the sudden infant death syndrome and the long-QT syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

30 September 2017

Infant sleep position and risk for sudden infant death syndrome: report of meeting held January 13 and 14, 1994, National Institutes of Health, Bethesda, MD.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

30 September 2017

The contribution of changes in the prevalence of prone sleeping position to the decline in sudden infant death syndrome in Tasmania

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

30 September 2017

Near-miss SIDS due to Brugada syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

28 June 2018

Infant sleep position following new AAP guidelines. American Academy of Pediatrics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

28 June 2018

Cardiac sodium channel dysfunction in sudden infant death syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

5 September 2018

Role of SCN5A Y1102 polymorphism in sudden cardiac death in blacks

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

5 September 2018

Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

5 September 2018

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430043

5 September 2018

Molecular diagnosis in a child with sudden infant death syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18452875

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18452875

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

American Academy of Pediatrics AAP Task Force on Infant Positioning and SIDS: Positioning and SIDS

1 reference

https://pubmed.ncbi.nlm.nih.gov/18452875

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic organization of the human SCN5A gene encoding the cardiac sodium channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/18452875

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.HRTHM.2008.02.012

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

ResearchGate publication ID

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