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

Treating hypoxia in a feeble breather with Rett syndrome.

Brain & development - 1 Mar 2013

Julu Peter O O, Witt Engerström Ingegerd, Hansen Stig, Apartopoulos Flora, Engerström Bengt

Abstract excerpt

Rett syndrome (RS) is a unique X-linked dominant neurodevelopmental disorder affecting 1 in 10,000 females. Mutations in the MECP2 gene located on Xq28 have been identified. Many of the characteristic features evolve due to immaturity of the brain in RS. Cardiorespiratory function should be investigated early to characterise the clinical phenotype of the person with RS because each of the three cardiorespiratory...

Read the complete abstract on PubMed

Topics

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

Share to Autonomic Nervous System
Share to Carbon Dioxide
Share to Methyl-CpG-Binding Protein 2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Respiration

Share to Respiratory Mechanics

Share to Rett Syndrome

Share to Vagus Nerve

Source

Identifiers

PMID: 22617859
DOI: 10.1016/j.braindev.2012.04.004

Genes

MECP2

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

Treating hypoxia in a feeble breather with Rett syndrome.PMID 22617859Read ↗

Systemic oxidative stress in classic Rett syndrome.Semantic proximity Read ↗

Loss of MeCP2 Function Across Several Neuronal Populations Impairs Breathing Response to Acute HypoxiaSemantic proximity Read ↗

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

Assessment of the maturity-related brainstem functions reveals the heterogeneous phenotypes and facilitates clinical management of Rett syndrome.Semantic proximity Read ↗

Hypoventilation in a case of congenital Rett syndromeSemantic proximity Read ↗

Central chemoreception: lessons from mouse and human genetics.Semantic proximity Read ↗

5-HTT polymorphisms in congenital central hypoventilation syndrome contribute to a modified resting CO2 set pointSemantic proximity Read ↗

Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2-/y knockout mice.Semantic proximity Read ↗

The kreisler mutation leads to the loss of intrinsically hypoxia-activated spots in the region of the retrotrapezoid nucleus/parafacial respiratory group.Semantic proximity Read ↗

CO<sub>2</sub>-Sensitive Preinspiratory Neurons of the Parafacial Respiratory Group Express Phox2b in the Neonatal RatSemantic proximity Read ↗

Autonomic nervous system dysregulation: breathing and heart rate perturbation during wakefulness in young girls with Rett syndrome.Semantic proximity Read ↗

Ventilatory responses to hypercapnia and hypoxia in heterozygous c-ret newborn mice.Semantic proximity Read ↗

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