Vagal and sympathetic heart rate and blood pressure control in adult onset PHOX2B mutation-confirmed congenital central hypoventilation syndrome. (Q48467269)

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scientific article published on 31 May 2007

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English	Vagal and sympathetic heart rate and blood pressure control in adult onset PHOX2B mutation-confirmed congenital central hypoventilation syndrome.	scientific article published on 31 May 2007

Statements

scholarly article

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

Vagal and sympathetic heart rate and blood pressure control in adult onset PHOX2B mutation-confirmed congenital central hypoventilation syndrome. (English)

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

congenital central hypoventilation syndrome

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5

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Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

author name string

André Diedrich

1

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

Beth A Malow

2

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

Nick A Antic

3

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

Kyoko Sato

4

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

Christopher J Mathias

6

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

David Robertson

7

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

Elizabeth M Berry-Kravis

8

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Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

Debra E Weese-Mayer

9

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

publication date

31 May 2007

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Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

Clinical Autonomic Research

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Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

17

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Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

3

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Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

177-185

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Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

https://scigraph.springernature.com/pub.10.1007/s10286-007-0421-4

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Ventilatory response to hyperoxia in newborn mice heterozygous for the transcription factor Phox2b.

1 reference

https://api.crossref.org/works/10.1007%2FS10286-007-0421-4

21 January 2018

Effect of viral infections on pulmonary function in patients with chronic obstructive pulmonary diseases

1 reference

https://api.crossref.org/works/10.1007%2FS10286-007-0421-4

21 January 2018

Adult identified with congenital central hypoventilation syndrome--mutation in PHOX2b gene and late-onset CHS.

1 reference

https://api.crossref.org/works/10.1007%2FS10286-007-0421-4

21 January 2018

Heart rate variability in congenital central hypoventilation syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS10286-007-0421-4

21 January 2018

Heart rate variability. Standards of measurement, physiological interpretation, and clinical use. Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital central hypoventilation syndrome: PHOX2B mutations and phenotype.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Short-term blood pressure and heart rate variability in congenital central hypoventilation syndrome (Ondine's curse).

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sleep-disordered breathing in newborn mice heterozygous for the transcription factor Phox2b.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term survival of a patient with congenital central hypoventilation syndrome despite the lack of continuous ventilatory support

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

General characteristics of sympathetic activity in human muscle nerves.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary alveolar hypoventilation and response to the respiratory stimulant almitrine

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatosensory, proprioceptive, and sympathetic activity in human peripheral nerves

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autonomic function in children with congenital central hypoventilation syndrome and their families

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution to the continuous indirect blood pressure measurement

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Twenty-four hour time domain heart rate variability and heart rate: relations to age and gender over nine decades.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Baroreflex regulation of heart rate and sympathetic vasomotor tone in women and men.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of congenital central hypoventilation syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reference values of indices of spontaneous baroreceptor reflex sensitivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression and interactions of the two closely related homeobox genes Phox2a and Phox2b during neurogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Idiopathic congenital central hypoventilation syndrome: diagnosis and management. American Thoracic Society

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In pursuit (and discovery) of a genetic basis for congenital central hypoventilation syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PHOX2B mutation-confirmed congenital central hypoventilation syndrome: presentation in adulthood.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic obstructive pulmonary disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541758

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heart rate variability: Standards of measurement, physiological interpretation, and clinical use

1 reference

27 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1093/OXFORDJOURNALS.EURHEARTJ.A014868

Identifiers

10.1007/S10286-007-0421-4

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

1 reference

Europe PubMed Central

11 February 2018

http://europepmc.org/abstract/MED/17541758

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