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

Autosomal dominant acute necrotizing encephalopathy.

Neurology - 22 Jul 2003

Neilson D E, Eiben R M, Waniewski S, Hoppel C L, Varnes M E, Bangert B A, Wiznitzer M, Warman M L, Kerr D S

Abstract excerpt

OBJECTIVE: To define the clinical and biochemical abnormalities of an autosomal dominant form of acute encephalopathy. METHODS: The clinical details of 11 affected family members in comparison with 63 unaffected relatives were analyzed. RESULTS: Affected children become comatose after onset of a...

Read the complete abstract on PubMed

Topics

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

Share to Diseases in Twins
Share to Electron Transport
Share to Fatal Outcome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Dominant

Share to Infections

Share to Mitochondrial Diseases

Share to Oxidative Phosphorylation

Source

Identifiers

PMID: 12874403
DOI: 10.1212/01.wnl.0000073544.28775.1a

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12874403-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Autosomal dominant acute necrotizing encephalopathy.PMID 12874403Read ↗

Familial acute necrotizing encephalopathy due to mutation in the RANBP2 gene.Semantic proximity Read ↗

Leigh disease with mitochondrial DNA A8344G mutation: case report and brief review.Semantic proximity Read ↗

Leigh-like subacute necrotising encephalopathy in Yorkshire Terriers: neuropathological characterisation, respiratory chain activities and mitochondrial DNA.Semantic proximity Read ↗

Walking difficulties and brainstem dysfunction: a case report of adult onset Leigh syndromeSemantic proximity Read ↗

Autosomal dominant acute necrotising encephalopathy: a case report with possible disease-expression modification by coincidental homocysteinuria.Semantic proximity Read ↗

Familial acute necrotizing encephalopathy temporally associated with SARS-CoV-2 infection: Two case reports and literature review.Semantic proximity Read ↗

Familial acute necrotizing encephalopathy with RANBP2 mutation: The first report in Northeast Asia.Semantic proximity Read ↗

Leigh syndrome: neuropathology and pathogenesis.Semantic proximity Read ↗

Sudden death in Leigh syndrome: an autopsy case.Semantic proximity Read ↗

Two siblings with acute necrotizing encephalopathy associated with variants of LARS1.Semantic proximity Read ↗

Leigh disease with brainstem involvement in complex I deficiency due to assembly factor NDUFAF2 defect.Semantic proximity Read ↗

Pathogenesis and Management of Acute Necrotizing Encephalopathy.Semantic proximity Read ↗

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