(Q41876433)

English

A case of adult-onset alexander disease featuring severe atrophy of the medulla oblongata and upper cervical cord on magnetic resonance imaging

scientific article published on September 2012

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

0 references

A case of adult-onset alexander disease featuring severe atrophy of the medulla oblongata and upper cervical cord on magnetic resonance imaging (English)

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Alexander disease

1 reference

based on heuristic

inferred from title

Satoshi Kuwabara

6

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

author name string

Tadahiro Yonezu

1

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Shoichi Ito

2

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Kazuaki Kanai

3

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Saeko Masuda

4

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Kazumoto Shibuya

5

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

publication date

1 September 2012

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Case reports in neurology

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

4

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

3

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

202-206

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

5 June 2018

Can MR imaging diagnose adult-onset Alexander disease?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

5 June 2018

Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

5 June 2018

Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

5 June 2018

Alexander disease: diagnosis with MR imaging.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

5 June 2018

Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

5 June 2018

Glial fibrillary acidic protein mutations in adult-onset Alexander disease: clinical features observed in 12 Japanese patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

18 August 2018

An adult form of Alexander disease: a novel mutation in glial fibrillary acidic protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

18 August 2018

Alexander disease: ventricular garlands and abnormalities of the medulla and spinal cord.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

18 August 2018

Adult Alexander's disease without leukoencephalopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

18 August 2018

Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

18 August 2018

Dominantly-inherited adult-onset leukodystrophy with palatal tremor caused by a mutation in the glial fibrillary acidic protein gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

18 August 2018

A case of adult-onset Alexander disease with Arg416Trp human glial fibrillary acidic protein gene mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

18 August 2018

Identification of GFAP gene mutation in hereditary adult-onset Alexander's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3506048

18 August 2018

Identifiers

10.1159/000345303

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

release_iecs57zlrrceni5yanaushxixy

1 reference

https://api.fatcat.wiki/v0/release/iecs57zlrrceni5yanaushxixy

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

ResearchGate publication ID

0 references

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