Re.: Clinical, radiological and pathological findings in an autosomal dominant leukodystrophy.

doi:10.1016/s0022-510x(01)00535-4

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

Community

Back to search

Article

Re.: Clinical, radiological and pathological findings in an autosomal dominant leukodystrophy.

Journal of the neurological sciences - 15 Jun 2001

Koeppen A H

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Central Nervous System
Share to Chromosomes, Human, Pair 5
Share to Genes, Dominant
Share to Heredodegenerative Disorders, Nervous System

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mutation

Share to Nerve Fibers, Myelinated

Share to Oligodendroglia

Source

Open in PubMed

Identifiers

PMID: 11486760
DOI: 10.1016/s0022-510x(01)00535-4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Re.: Clinical, radiological and pathological findings in an autosomal dominant leukodystrophy.PMID 11486760Read ↗

Autosomal dominant leukodystrophy caused by lamin B1 duplications a clinical and molecular case study of altered nuclear function and disease.Semantic proximity Read ↗

Radiological findings in siblings with dysferlin mutation with diverse phenotype.Semantic proximity Read ↗

Progeria: a laminopathy of special interest.Semantic proximity Read ↗

A novel mutation of the arylsulfatase A gene in late-onset metachromatic leukodystrophy.Semantic proximity Read ↗

Metachromatic leukodystrophy: Disease spectrum and approaches for treatmentSemantic proximity Read ↗

Leukodystrophy Imaging: Insights for Diagnostic DilemmasSemantic proximity Read ↗

Genetic, clinical, and morphologic heterogeneity in Alport's syndrome.Semantic proximity Read ↗

A monogenetic disorder yet multiple and varied clinical manifestations.Semantic proximity Read ↗

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