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

Methionine metabolism and phenotypic variability in X-linked adrenoleukodystrophy.

Neurology - 14 Feb 2006

Linnebank M, Kemp S, Wanders R J A, Kleijer W J, van der Sterre M L T, Gärtner J, Fliessbach K, Semmler A, Sokolowski P, Köhler W, Schlegel U, Schmidt S, Klockgether T, Wüllner U

Abstract excerpt

A combined genotype of polymorphisms of methionine metabolism has been associated with CNS demyelination in methotrexate-treated patients. Within a sample of 86 patients with X-linked adrenoleukodystrophy, this genotype was overrepresented in a subgroup of 15 patients with adrenomyeloneuropathy (...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Adrenoleukodystrophy
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Genetic Variation

Share to Genotype

Share to Methionine

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 16476952
DOI: 10.1212/01.wnl.0000196491.42058.6f

Genes

AMN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16476952-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Methionine metabolism and phenotypic variability in X-linked adrenoleukodystrophy.PMID 16476952Read ↗

Genetic variants of methionine metabolism and X-ALD phenotype generation: results of a new study sample.Semantic proximity Read ↗

The cystathionine beta-synthase variant c.844_845ins68 protects against CNS demyelination in X-linked adrenoleukodystrophy.Semantic proximity Read ↗

[Association of genetic polymorphisms in methionine metabolism genes with X-linked adrenoleukodystrophy].Semantic proximity Read ↗

X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy.Semantic proximity Read ↗

Progress in X-linked adrenoleukodystrophySemantic proximity Read ↗

Clinical aspects of adrenoleukodystrophy and adrenomyeloneuropathy.Semantic proximity Read ↗

Epigenomic signature of adrenoleukodystrophy predicts compromised oligodendrocyte differentiation.Semantic proximity Read ↗

Evolution of phenotypes in adult male patients with X-linked adrenoleukodystrophy.Semantic proximity Read ↗

Cerebral adrenoleukodystrophy (ALD) in only one of monozygotic twins with an identical ALD genotype.Semantic proximity Read ↗

Diagnosis of X-adrenoleucodystrophy phenotypic variants.Semantic proximity Read ↗

Variability of endocrinological dysfunction in 55 patients with X-linked adrenoleucodystrophy: clinical, laboratory and genetic findings.Semantic proximity Read ↗

Phenotypic heterogeneity of an adult form of adrenoleukodystrophy in monozygotic twins.Semantic proximity Read ↗

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