(Q37771900)

22 August 2017

1 reference

title

Gene variants predisposing to SIDS: current knowledge (English)

1 reference

22 August 2017

Siri H Opdal

1

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22 August 2017

Torleiv O Rognum

series ordinal

2

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22 August 2017

publication date

11 July 2010

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Forensic Science Medicine and Pathology

22 August 2017

published in

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22 August 2017

volume

7

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22 August 2017

issue

1

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22 August 2017

page(s)

26-36

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Biochemical and immunological studies in SIDS victims. Clues to understanding the death mechanism

22 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

A perspective on neuropathologic findings in victims of the sudden infant death syndrome: the triple-risk model

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Cardiac sodium channel dysfunction in sudden infant death syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Sleeping position and sudden infant death syndrome (SIDS): effect of an intervention programme to avoid prone sleeping.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Changes in the epidemiological pattern of sudden infant death syndrome in southeast Norway, 1984-1998: implications for future prevention and research

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Major epidemiological changes in sudden infant death syndrome: a 20-year population-based study in the UK.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Sudden infant death syndrome, infection and inflammatory responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

SIDS cases have increased levels of interleukin-6 in cerebrospinal fluid

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Interleukin-1 as intermediary causing prolonged sleep apnea and SIDS during respiratory infections

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Interleukin-6 and the serotonergic system of the medulla oblongata in the sudden infant death syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Brainstem serotonergic deficiency in sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Modulation of serotonin transporter function by interleukin-4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Infectious diseases associated with complement deficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

IL-10 gene polymorphisms are associated with infectious cause of sudden infant death

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Interleukin 10 genotype as a risk factor for sudden infant death syndrome: determination of IL-10 genotype from wax-embedded postmortem samples.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Interleukin-10 and sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

TNF-alpha promoter polymorphisms in sudden infant death

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

TNF-alpha and IL-10 gene polymorphisms versus cardioimmunological responses in sudden infant death.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Distribution of interleukin-1 receptor antagonist genotypes in sudden unexpected death in infancy (SUDI); unexplained SUDI have a higher frequency of allele 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

IL-1 gene cluster polymorphisms and sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Differential regulation of interleukin-10 production by genetic and environmental factors--a twin study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Influence of interleukin-1 receptor antagonist gene polymorphism on disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Interleukin-6 promoter haplotypes and interleukin-6 cytokine responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Allele-specific binding of the ubiquitous transcription factor OCT-1 to the functional single nucleotide polymorphism (SNP) sites in the tumor necrosis factor-alpha gene (TNFA) promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Interaction of Gbeta3s, a splice variant of the G-protein Gbeta3, with Ggamma- and Galpha-proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

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/10.1007%2FS12024-010-9182-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Heterozygous nonsense SCN5A mutation W822X explains a simultaneous sudden infant death syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Contribution of long-QT syndrome genetic variants in sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Cardiac ion channel gene mutations in sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

SNP association and sequence analysis of the NOS1AP gene in SIDS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

The brainstem and serotonin in the sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Medullary serotonin defects and respiratory dysfunction in sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Serotonin transporter gene variation is a risk factor for sudden infant death syndrome in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Serotonin transporter gene variation in sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Multiple serotonergic brainstem abnormalities in sudden infant death syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

No association of serotonin transporter gene variation with sudden infant death syndrome (SIDS) in Caucasians

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Sudden infant death syndrome and sudden intrauterine unexplained death: correlation between hypoplasia of raphé nuclei and serotonin transporter gene promoter polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

HTR2A variation and sudden infant death syndrome: a case-control analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Sudden infant death syndrome: rare mutation in the serotonin system FEV gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase-activating polypeptide (PACAP).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Sudden infant death syndrome is not associated with the mutation of PHOX2B gene, a major causative gene of congenital central hypoventilation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Genetic investigation of the TSPYL1 gene in sudden infant death syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Assessment of growth in sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Functional allelic heterogeneity and pleiotropy of a repeat polymorphism in tyrosine hydroxylase: prediction of catecholamines and response to stress in twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

NHE3 in the human brainstem: implication for the pathogenesis of the sudden infant death syndrome (SIDS)?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Prevalence of medium-chain acyl-coenzyme A dehydrogenase deficiency in the sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Homozygosity for a severe novel medium-chain acyl-CoA dehydrogenase (MCAD) mutation IVS3-1G>C that leads to introduction of a premature termination codon by complete missplicing of the MCAD mRNA and is associated with phenotypic diversity ranging fro

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Identification of novel polymorphisms in the glucokinase and glucose-6-phosphatase genes in infants who died suddenly and unexpectedly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Genetic variation in hepatic glucose-6-phosphatase system genes in cases of sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

An assessment of behavioural characteristics in infants who died of sudden infant death syndrome using the Early Infancy Temperament Questionnaire.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Mitochondrial myopathy with tRNA(Leu(UUR)) mutation and complex I deficiency responsive to riboflavin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Sudden infant death. Overheating and cot death

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Human heat shock protein gene polymorphisms and sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Maternal cigarette smoking, metabolic gene polymorphism, and infant birth weight

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Flavin-containing monooxygenase genetic polymorphism: impact on chemical metabolism and drug development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Copy number variations in three children with sudden infant death.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

The sudden infant death syndrome gene: does it exist?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Sudden infant death syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Mutations in the HERG K+-ion channel: A novel link between long QT syndrome and sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Molecular diagnosis in a child with sudden infant death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

Is the medium-chain acyl-CoA dehydrogenase G985 mutation involved in sudden infant death in Norway?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

The prevalence of the G985 allele of medium-chain acyl-CoA dehydrogenase deficiency among sudden infant death victims and healthy newborns in northern Germany

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12024-010-9182-9

The G protein beta3 subunit splice variant Gbeta3-s causes enhanced chemotaxis of human neutrophils in response to interleukin-8

21 January 2018

1 reference

12 December 2020

Impact of sodium/proton exchanger 3 gene variants on sudden infant death syndrome

1 reference

12 December 2020

Covalent binding properties of the C4A and C4B isotypes of the fourth component of human complement on several C1-bearing cell surfaces

1 reference

12 December 2020

IL6 G-174C associated with sudden infant death syndrome in a Caucasian Australian cohort

1 reference

12 December 2020

[Crib death in the eastern regions of Norway 1984-1992. A survey of risk factors]

1 reference

12 December 2020

Rapid testing for the MCAD G583A mutation, by PCR-mediated site directed mutagenesis, in an Australian population of SIDS patients

1 reference

12 December 2020

IL-6 cerebrospinal fluid levels are related to laryngeal IgA and epithelial HLA-DR response in sudden infant death syndrome

1 reference

12 December 2020

Relationship of sudden infant death syndrome to maternal smoking during and after pregnancy

1 reference

12 December 2020

Increased number of substitutions in the D-loop of mitochondrial DNA in the sudden infant death syndrome

1 reference

12 December 2020

A mitochondrial DNA polymorphism associated with cardiac arrhythmia investigated in sudden infant death syndrome

1 reference

12 December 2020

A founder mutation of the potassium channel KCNQ1 in long QT syndrome: implications for estimation of disease prevalence and molecular diagnostics

1 reference

12 December 2020

Possible role of mtDNA mutations in sudden infant death

1 reference

12 December 2020

A common FMO3 polymorphism may amplify the effect of nicotine exposure in sudden infant death syndrome (SIDS).

1 reference

12 December 2020

Up-regulated epithelial expression of HLA-DR and secretory component in salivary glands: reflection of mucosal immunostimulation in sudden infant death syndrome

1 reference

12 December 2020

Are substitutions in the first hypervariable region of the mitochondrial DNA displacement-loop in sudden infant death syndrome due to maternal inheritance?

1 reference

12 December 2020

Prolonged QT interval and sudden infant death--report of two cases

1 reference

12 December 2020

Sudden infant death: no evidence for linkage to common polymorphisms in the uncoupling protein-1 and the beta3-adrenergic receptor genes

1 reference

12 December 2020

The IL6 -174G/C polymorphism and sudden infant death syndrome

1 reference

12 December 2020

Sudden infant death syndrome victims show local immunoglobulin M response in tracheal wall and immunoglobulin A response in duodenal mucosa

1 reference

12 December 2020

Scottish frequency of the common G985 mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene and the role of MCAD deficiency in sudden infant death syndrome (SIDS)

1 reference

12 December 2020

Genetic variation in the HTR1A gene and sudden infant death syndrome

1 reference

12 December 2020

Possible association of sudden infant death with partial complement C4 deficiency revealed by post-mortem DNA typing of HLA class II and III genes

1 reference

12 December 2020

Sleep and cardiorespiratory characteristics of infant victims of sudden death: a prospective case-control study

1 reference

12 December 2020

Aquaporin-4 gene variation and sudden infant death syndrome

1 reference

12 December 2020

Association of IL-10 genotype with sudden infant death syndrome

1 reference

12 December 2020

The complement component C4 in sudden infant death

1 reference

12 December 2020

Sudden infant death syndrome not caused by Norwegian Jervell and Lange-Nielsen mutations

1 reference

12 December 2020

Incongruent cerebral growth in sudden infant death syndrome

1 reference

12 December 2020

The G protein beta3 subunit 825C allele is associated with sudden infant death due to infection

1 reference

12 December 2020

Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene

1 reference

12 December 2020

Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis

1 reference

12 December 2020

Thermal stress, sleeping position, and the sudden infant death syndrome

1 reference

12 December 2020

Frequency of G-985 mutation in medium chain acyl-coenzyme A dehydrogenase (MCAD) deficiency in sudden infant death syndrome (SIDS)

1 reference

12 December 2020

Surfactant protein A and D gene polymorphisms and protein expression in victims of sudden infant death

1 reference

12 December 2020

The frequency of a disease-causing point mutation in the gene coding for medium-chain acyl-CoA dehydrogenase in sudden infant death syndrome

1 reference

12 December 2020

Interleukin 1-beta responses to bacterial toxins and sudden infant death syndrome

1 reference

12 December 2020

Phenotypic manifestations of the OCTN2 V295X mutation: sudden infant death and carnitine-responsive cardiomyopathy in Roma families

1 reference

12 December 2020

Mitochondrial DNA point mutations detected in four cases of sudden infant death syndrome

1 reference

12 December 2020

Susceptibility to lung cancer in light smokers associated with CYP1A1 polymorphisms in Mexican- and African-Americans

1 reference

12 December 2020

Sudden Infant Death Syndrome: review of implicated genetic factors

1 reference

12 December 2020

Medium-chain acyl-CoA dehydrogenase deficiency does not correlate with apparent life-threatening events and the sudden infant death syndrome: results from phenylpropionate loading tests and DNA analysis

1 reference

12 December 2020

3' UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: haplotype analysis

1 reference

12 December 2020

Mitochondrial tRNA genes and flanking regions in sudden infant death syndrome

1 reference

12 December 2020

Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene

1 reference

12 December 2020

Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential

1 reference

12 December 2020

Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome

1 reference

12 December 2020

Upregulation of reactive oxygen species generation and phagocytosis, and increased apoptosis in human neutrophils during severe sepsis and septic shock

1 reference

12 December 2020

Apolipoprotein E e4 and its prevalence in early childhood death due to sudden infant death syndrome or to recognised causes

1 reference

12 December 2020

Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected death

1 reference

12 December 2020

Analysis of the mitochondrial genome in sudden infant death syndrome

1 reference

12 December 2020

Cytokine gene polymorphisms and sudden infant death syndrome

1 reference

12 December 2020

Association of sudden infant death syndrome with VEGF and IL-6 gene polymorphisms

1 reference

12 December 2020

The A985 to G mutation of the medium-chain acyl-CoA dehydrogenase gene and sudden infant death syndrome in Normandy

1 reference

12 December 2020

Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease

1 reference

12 December 2020

Genetic polymorphism of CYP genes, alone or in combination, as a risk modifier of tobacco-related cancers.

1 reference

12 December 2020

10.1007/S12024-010-9182-9

Identifiers

DOI

1 reference

22 August 2017

1 reference