(Q46665134)

English

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

scientific article published on 2 April 2008

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scholarly article

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

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

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

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Anna Maria Lavezzi

4

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

Stefano Parmigiani

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Stefano Parmigiani

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8

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Luigi Matturri

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

author name string

Francesco Nonnis Marzano

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

Milena Maldini

2

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

Laura Filonzi

3

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

Cinzia Magnani

6

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

Giulio Bevilacqua

7

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

publication date

2 April 2008

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

91

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

485-491

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Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

Multiple serotonergic brainstem abnormalities in sudden infant death syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Thermal insulation and SIDS-an investigation of selected 'Eastern' and 'Western' infant bedding combinations.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Recent trend of the incidence of sudden infant death syndrome in Japan

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Medium-chain acyl-coenzyme A dehydrogenase deficiency and sudden infant death

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Sudden Infant Death Syndrome: review of implicated genetic factors

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Genetics. Crib death exoneration could usher in new gene tests

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Update on sudden infant death syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Serotonergic brainstem abnormalities in Northern Plains Indians with the sudden infant death syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

A serotonin malfunction hypothesis by finding clear mutual relationships between several risk factors and symptoms associated with sudden infant death syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Hypoplasia of the arcuate nucleus and maternal smoking during pregnancy in sudden unexplained perinatal and infant death

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

MAOA promoter polymorphism and attention deficit hyperactivity disorder (ADHD) in indian children

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Allelic Variation of Human Serotonin Transporter Gene Expression

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

A serotonin transporter gene intron 2 polymorphic region, correlated with affective disorders, has allele-dependent differential enhancer-like properties in the mouse embryo

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Population studies of polymorphisms of the serotonin transporter protein gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Robust and tissue-specific expression of TPH2 versus TPH1 in rat raphe and pineal gland

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Association of autism severity with a monoamine oxidase A functional polymorphism.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

DNA extraction from archival formalin-fixed, paraffin-embedded tissue sections based on the antigen retrieval principle: heating under the influence of pH.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Detection of manipulation in doping control urine sample collection: a multidisciplinary approach to determine identical urine samples

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Serotonin and aggressive behavior in rodents and nonhuman primates: predispositions and plasticity

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2008.01.010

7 January 2021

Identifiers

10.1016/J.YGENO.2008.01.010

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

1 reference

Europe PubMed Central

24 December 2017

http://europepmc.org/abstract/MED/18387780

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