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

Cerebrospinal fluid monoamines in Prader-Willi syndrome.

Biological psychiatry - 15 Dec 1998

Akefeldt A, Ekman R, Gillberg C, Månsson J E

Abstract excerpt

BACKGROUND: The behavioral phenotype of Prader-Willi syndrome (PWS) suggests hypothalamic dysfunction and altered neurotransmitter regulation. The purpose of this study was to examine whether there was any difference in the concentrations of monoamine metabolites in the cerebrospinal fluid (CSF)...

Topics

Adolescent
Adult
Age Factors
Autistic Disorder
Birth Weight
Body Mass Index
Child
Child, Preschool
Female
Homovanillic Acid
Humans
Hydroxyindoleacetic Acid
Infant

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Intelligence Tests

Male

Methoxyhydroxyphenylglycol

Neurotransmitter Agents

Obesity

Source

Identifiers

PMID: 9861475
DOI: 10.1016/s0006-3223(97)00519-2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9861475-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 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.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cerebrospinal fluid monoamines in Prader-Willi syndrome.PMID 9861475Read ↗

Hypersomnia in the Prader Willi syndrome: clinical-electrophysiological features and underlying factors.Semantic proximity Read ↗

TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome.Semantic proximity Read ↗

[Behavioural phenotypes in Prader-Willi syndrome].Semantic proximity Read ↗

Phenotypic features of children with neurodevelopmental diseases in relation to biogenic amines.Semantic proximity Read ↗

Klinefelter's syndrome and Prader-Willi syndrome: a rare combination.Semantic proximity Read ↗

Psychotic disorders in Prader–Willi syndromeSemantic proximity Read ↗

Catecholamine phenotyping: clues to the diagnosis, treatment, and pathophysiology of neurogenetic disorders.Semantic proximity Read ↗

Increased plasma chemokine levels in children with Prader-Willi syndrome.Semantic proximity Read ↗

The relationship between endogenous oxytocin and vasopressin levels and the Prader-Willi syndrome behaviour phenotype.Semantic proximity Read ↗

Central adrenal insufficiency in young adults with Prader-Willi syndrome.Semantic proximity Read ↗

Monoamine related functional gene variants and relationships to monoamine metabolite concentrations in CSF of healthy volunteers.Semantic proximity Read ↗

Tentative classification of neuropsychiatric disturbances in Prader-Willi syndrome.Semantic proximity Read ↗

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