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

Neuroferritinopathy: a neurodegenerative disorder associated with L-ferritin mutation.

Best practice & research. Clinical haematology - 1 Jun 2005

Levi Sonia, Cozzi Anna, Arosio Paolo

Abstract excerpt

Neuroferritinopathy is a dominantly inherited movement disorder characterized by deposition of iron and ferritin in the brain, normal or low serum ferritin levels, and highly variable clinical features. The disease, also named dominant adult-onset basal ganglia disease, is associated with a nucle...

Read the complete abstract on PubMed

Topics

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

Share to Apoferritins
Share to Basal Ganglia Diseases
Share to Ferritins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Dominant

Share to Movement Disorders

Share to Neurodegenerative Diseases

Share to Protein Structure, Secondary

Source

Identifiers

PMID: 15737889
DOI: 10.1016/j.beha.2004.08.021

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-15737889-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Neuroferritinopathy: a neurodegenerative disorder associated with L-ferritin mutation.PMID 15737889Read ↗

A novel ferritin light chain mutation in neuroferritinopathy with an atypical presentation.Semantic proximity Read ↗

Oxidative stress and cell death in cells expressing L-ferritin variants causing neuroferritinopathy.Semantic proximity Read ↗

Neuroferritinopathy.Semantic proximity Read ↗

Mutant ferritin L-chains that cause neurodegeneration act in a dominant-negative manner to reduce ferritin iron incorporation.Semantic proximity Read ↗

Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease.Semantic proximity Read ↗

Neuroferritinopathy.Semantic proximity Read ↗

Neuroferritinopathy.Semantic proximity Read ↗

[Clinical features of neuroferritinopathy].Semantic proximity Read ↗

Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights.Semantic proximity Read ↗

A 3'-truncating FTL mutation associated with hypoferritinemia without neuroferritinopathy.Semantic proximity Read ↗

Expression of a mutant form of the ferritin light chain gene induces neurodegeneration and iron overload in transgenic mice.Semantic proximity Read ↗

Neuroferritinopathy: a new inborn error of iron metabolism.Semantic proximity Read ↗

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