Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Neurocognitive monitoring in congenital central hypoventilation syndrome with the NIH Toolbox®.

Pediatric pulmonology - 1 Sept 2022

Welbel Remi Z, Rand Casey M, Zhou Amy, Fadl-Alla Allaa, Chen Maida Lynn, Weese-Mayer Debra E, Zelko Frank A

Abstract excerpt

Congenital central hypoventilation syndrome (CCHS) is a rare neurocristopathy, caused by mutations in the paired-like homeobox gene PHOX2B, which alters control of breathing and autonomic nervous system regulation, necessitating artificial ventilation as life-support. A broad range of neurocognitive performance has been reported in CCHS, including an array of cognitive deficits. We administered the NIH Toolbox®...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Homeodomain Proteins
Share to Hypoventilation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mental Status and Dementia Tests

Share to Mutation

Share to Sleep Apnea, Central

Share to Transcription Factors

Source

Open in PubMed Open full text

Identifiers

PMID: 35574731
DOI: 10.1002/ppul.25973
PMCID: PMC9541049

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Neurocognitive monitoring in congenital central hypoventilation syndrome with the NIH Toolbox®.PMID 35574731Read ↗

Congenital Central Hypoventilation Syndrome: Neurocognition Already Reduced in Preschool-Aged Children.Semantic proximity Read ↗

A nonverbal learning disability in a case of central hypoventilation syndrome without a PHOX2B gene mutation.Semantic proximity Read ↗

Congenital central hypoventilation syndrome: neurocognitive functioning in school age children.Semantic proximity Read ↗

Neurocognitive functioning in individuals with congenital central hypoventilation syndrome.Semantic proximity Read ↗

Neurocognition in Congenital Central Hypoventilation Syndrome: influence of genotype and ventilation method.Semantic proximity Read ↗

Psychometric Properties of the NIH Toolbox Cognition and Emotion Batteries Among Children and Adolescents with Congenital Heart DefectsSemantic proximity Read ↗

An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management.Semantic proximity Read ↗

Remote assessment of the Penn computerised neurocognitive battery in individuals with 22q11.2 deletion syndrome.Semantic proximity Read ↗

Identification of cognitive phenotypes in temporal lobe epilepsy and genetic generalized epilepsy using robotic assessment.Semantic proximity Read ↗

Residual chemosensitivity to ventilatory challenges in genotyped congenital central hypoventilation syndrome.Semantic proximity Read ↗

Later Onset Congenital Central Hypoventilation Syndrome.Semantic proximity Read ↗

Congenital Central Hypoventilation Syndrome (CCHS): Patient Quality of Life and Caregiver BurdenSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.