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

Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism.

Journal of medical genetics - 1 Mar 2003

Crow Y J, Black D N, Ali M, Bond J, Jackson A P, Lefson M, Michaud J, Roberts E, Stephenson J B P, Woods C G, Lebon P

Abstract excerpt

Aicardi-Goutiéres syndrome (AGS) is an early onset, progressive encephalopathy characterised by calcification of the basal ganglia, white matter abnormalities, and a chronic cerebrospinal fluid (CSF) lymphocytosis. Cree encephalitis shows phenotypic overlap with AGS although the conditions have been considered distinct because of immunological abnormalities observed in Cree encephalitis. We report that levels of...

Read the complete abstract on PubMed

Topics

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

Share to Basal Ganglia Diseases
Share to Calcinosis

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

Share to Chromosomes, Human, Pair 3

Share to Encephalitis

Share to Indians, North American

Share to Interferon-alpha

Share to Lod Score

Share to Lymphocytosis

Source

Open in PubMed Open full text

Identifiers

PMID: 12624136
DOI: 10.1136/jmg.40.3.183
PMCID: PMC1735395

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism.PMID 12624136Read ↗

Interferon-related transcriptome alterations in the cerebrospinal fluid cells of Aicardi-Goutières patients.Semantic proximity Read ↗

Aicardi-Goutières syndrome (AGS).Semantic proximity Read ↗

Aicardi-Goutières syndrome: A monogenic type I interferonopathy.Semantic proximity Read ↗

The prototypical interferonopathy: Aicardi-Goutières syndrome from bedside to bench.Semantic proximity Read ↗

Aicardi-Goutières syndrome: an expanding phenotype.Semantic proximity Read ↗

Clinical and neuroradiologic variability of Aicardi-Goutiéres syndrome: Two siblings with RNASEH2C mutation and a boy with TREX1 mutation.Semantic proximity Read ↗

Aicardi–Goutieres syndrome: from patients to genes and beyondSemantic proximity Read ↗

Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutières syndrome.Semantic proximity Read ↗

Treatments in Aicardi–Goutières syndromeSemantic proximity Read ↗

Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature ReviewSemantic proximity Read ↗

Spastic paraparesis and marked improvement of leukoencephalopathy in Aicardi-Goutières syndrome.Semantic proximity Read ↗

Analysis of clinical characteristics of children with Aicardi-Goutieres syndrome in China.Semantic proximity Read ↗

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