(Q24518290)

English

The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis).

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

1 reference

Europe PubMed Central

The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis). (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

0 references

cerebrospinal fluid

0 references

author name string

Tolmie JL

1

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

Shillito P

2

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

Hughes-Benzie R

3

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

Stephenson JB

4

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

language of work or name

0 references

publication date

1 November 1995

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

32

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

881-884

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

Encephalitis among Cree children in northern Quebec

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

24 March 2017

Autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

27 September 2017

Transmembrane signaling by IFN-alpha.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

27 September 2017

A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

27 September 2017

Idiopathic familial cerebrovascular ferrocalcinosis (Fahr's disease) and review of differential diagnosis of intracranial calcification in children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

27 September 2017

Familial calcification of the basal ganglia with cerebrospinal fluid pleocytosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

27 September 2017

Infantile familial encephalopathy with cerebral calcifications and leukodystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

27 September 2017

Encephalopathy with calcifications of the basal ganglia in children. A reappraisal of Fahr's syndrome with respect to 14 new cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

27 September 2017

Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

27 September 2017

Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly, and retinal degeneration: two sibs confirming a probably distinct entity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

27 September 2017

Microcephaly with extensive calcium deposits and demyelination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

30 May 2018

Two siblings with microcephaly associated with calcification of cerebral white matter

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

30 May 2018

A syndrome with intracranial calcification and microcephaly in two sibs, resembling intrauterine infection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

30 May 2018

Intrathecal synthesis of interferon-alpha in infants with progressive familial encephalopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

30 May 2018

Magnetic resonance imaging in infantile encephalopathy with cerebral calcification and leukodystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

30 May 2018

Encephalopathy of Infancy with Intracerebral Calcification and Chronic Spinal Fluid Lymphocytosis - Another Case of the Aicardi-Goutières Syndrome

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

30 May 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

29 November 2018

Skeletal dysplasia, intracerebral calcifications, optic atrophy, hearing impairment, and mental retardation: nosology of dysosteosclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

30 May 2018

Cerebral calcifications and cerebellar hypoplasia in two children: clinical, radiologic and neuropathological studies--a separate neurodevelopmental entity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051740

29 November 2018

[Syndrome of calcifications of basal ganglia, leukodystrophy and chronic lymphomonocytic pleocytosis of the cerebrospinal fluid: report of a case]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8592332

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Diffuse symmetric calcification in a syndrome including microcephaly and meningoencephalitis]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8592332

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Leukodystrophy with strio-cerebellar calcification, microcephaly and dwarfism]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8592332

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of progressive familial encephalopathy in infancy with calcification of the basal ganglia and chronic cerebrospinal fluid lymphocytosis

1 reference

https://api.crossref.org/works/10.1136%2FJMG.32.11.881

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1136/JMG.32.11.881

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

PMC publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q24518290&oldid=1475449413"