Phenotypic features of children with neurodevelopmental diseases in relation to biogenic amines.

doi:10.1016/j.resp.2014.12.007

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

Back to search

Article

Phenotypic features of children with neurodevelopmental diseases in relation to biogenic amines.

Respiratory physiology & neurobiology - 1 Apr 2015

Szymańska Krystyna, Kuśmierska Katarzyna, Nowacka Maria, Sykut-Cegielska Jolanta, Demkow Urszula

Abstract excerpt

Disruption of monoamines metabolism leads to diverse manifestations, including developmental, movement and respiratory dysfunctions. We aimed to correlate clinical phenotypes of 55 children with neurodevelopmental disorders with dopamine (HVA) and serotonin (5-HIIA) metabolites in CSF. Decreased level of at least one metabolite was documented in 49.1% patients. Both metabolites were significantly lower in...

Topics

Adolescent
Adult
Biogenic Amines
Child
Child, Preschool
Disease Progression
Female
Follow-Up Studies
Humans
Infant
Logistic Models
Male
Multivariate Analysis
Neurodevelopmental Disorders
Phenotype
Young Adult

Source

Open in PubMed

Identifiers

PMID: 25514185
DOI: 10.1016/j.resp.2014.12.007

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics