(Q48562005)

English

Functional brain deficits in congenital central hypoventilation syndrome: commentary on the articles by Woo et al. on page 510 and Macey et al. on page 500.

scientific article published on 17 February 2005

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scholarly article

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Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/15718351

Functional brain deficits in congenital central hypoventilation syndrome: commentary on the articles by Woo et al. on page 510 and Macey et al. on page 500. (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/15718351

congenital central hypoventilation syndrome

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author name string

Claude Gaultier

1

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Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/15718351

language of work or name

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publication date

17 February 2005

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Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/15718351

Pediatric Research

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Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/15718351

57

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Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/15718351

4

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/15718351

471-472

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/15718351

https://scigraph.springernature.com/pub.10.1203/01.pdr.0000158667.41282.f1

0 references

FMRI responses to hyperoxia in congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

Aberrant neural responses to cold pressor challenges in congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

Congenital central hypoventilation syndrome: an update.

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

Hypoxic and hypercapnic ventilatory responses in awake children with congenital central hypoventilation syndrome.

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

Heart rate variability in congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

Temporal trends of cardiac and respiratory responses to ventilatory challenges in congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

24-hour BP in children with congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

Ventilatory response to exercise in children with congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

Anxiety and congenital central hypoventilation syndrome.

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

Genetics and early disturbances of breathing control

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

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.0000158667.41282.F1

21 January 2018

PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

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.0000158667.41282.F1

21 January 2018

Phox2b controls the development of peripheral chemoreceptors and afferent visceral pathways.

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

fMRI signal changes in response to forced expiratory loading in congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

Hypoxia reveals posterior thalamic, cerebellar, midbrain, and limbic deficits in congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000158667.41282.F1

21 January 2018

Identifiers

10.1203/01.PDR.0000158667.41282.F1

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/15718351

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/15718351

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