(Q44969039)

English

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

scientific article published on 7 July 2004

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scholarly article

1 reference

Europe PubMed Central

7 December 2017

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

1 reference

Europe PubMed Central

7 December 2017

sudden infant death syndrome

1 reference

based on heuristic

inferred from title

Mary L. Marazita

7

object named as

Mary L Marazita

1 reference

Europe PubMed Central

7 December 2017

author name string

Debra E Weese-Mayer

1

1 reference

Europe PubMed Central

7 December 2017

Elizabeth M Berry-Kravis

2

1 reference

Europe PubMed Central

7 December 2017

Lili Zhou

3

1 reference

Europe PubMed Central

7 December 2017

Brion S Maher

4

1 reference

Europe PubMed Central

7 December 2017

Mark E Curran

5

1 reference

Europe PubMed Central

7 December 2017

Jean M Silvestri

6

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Europe PubMed Central

7 December 2017

language of work or name

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publication date

7 July 2004

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Europe PubMed Central

7 December 2017

Pediatric Research

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Europe PubMed Central

7 December 2017

56

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Europe PubMed Central

7 December 2017

3

1 reference

Europe PubMed Central

7 December 2017

391-395

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Europe PubMed Central

7 December 2017

https://scigraph.springernature.com/pub.10.1203/01.pdr.0000136285.91048.4a

0 references

Defining the sudden infant death syndrome (SIDS): deliberations of an expert panel convened by the National Institute of Child Health and Human Development

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Annual summary of vital statistics--2002.

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Decreased serotonergic receptor binding in rhombic lip-derived regions of the medulla oblongata in the sudden infant death syndrome.

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Alteration of serotonergic receptors in the brain stems of human patients with respiratory disorders

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Interaction between bedding and sleeping position in the sudden infant death syndrome: a population based case-control study

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Thermal environment and sudden infant death syndrome: case-control study

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Neurocardiogenic syncope: a model for SIDS.

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Polysomnographic study of the autonomic nervous system in potential victims of sudden infant death syndrome.

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Symptoms, sweating and reactivity of infants who die of SIDS compared with community controls. New Zealand National Cot Death Study Group

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Decreased autonomic responses to obstructive sleep events in future victims of sudden infant death syndrome.

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Case/control family study of autonomic nervous system dysfunction in idiopathic congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Congenital central hypoventilation syndrome: inheritance and relation to sudden infant death syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Molecular analysis of congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

MASH1 maintains competence for BMP2-induced neuronal differentiation in post-migratory neural crest cells

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Mammalian achaete-scute homolog 1 is required for the early development of olfactory and autonomic neurons

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Specification of neurotransmitter identity by Phox2 proteins in neural crest stem cells

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Mutations of the RET-GDNF signaling pathway in Ondine's curse

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Point mutation in exon 12 of the receptor tyrosine kinase proto-oncogene RET in Ondine-Hirschsprung syndrome.

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Congenital central hypoventilation syndrome associated with Hirschsprung's disease: mutation analysis of the RET and endothelin-signaling pathways

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Congenital central hypoventilation syndrome: a novel mutation of the RET gene in an isolated case

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Association of germline mutations and polymorphisms of the RET proto-oncogene with idiopathic congenital central hypoventilation syndrome in 33 patients

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

RET proto-oncogene is important for the development of respiratory CO2 sensitivity.

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Impaired ventilatory responses to hypoxia in mice deficient in endothelin-converting-enzyme-1.

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Rnx deficiency results in congenital central hypoventilation

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Mutational analysis of the RNX gene in congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

Exclusion ofRNX as a major gene in congenital central hypoventilation syndrome (CCHS, Ondine's curse)

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000136285.91048.4A

21 January 2018

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10.1203/01.PDR.0000136285.91048.4A

1 reference

Europe PubMed Central

7 December 2017

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1 reference

Europe PubMed Central

7 December 2017

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