(Q34144248)

31 July 2017

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title

Alexander disease: a review and the gene (English)

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31 July 2017

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Anne B Johnson

1

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31 July 2017

publication date

1 June 2002

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International Journal of Developmental Neuroscience

31 July 2017

published in

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31 July 2017

volume

20

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31 July 2017

issue

3-5

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31 July 2017

page(s)

391-394

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

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

A novel mutation in glial fibrillary acidic protein gene in a patient with Alexander disease

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Ultrastructural immunogold labeling of glial filaments in osmicated and unosmicated epoxy-embedded tissue.

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Alexander's disease. A disease of astrocytes.

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Advanced lipid peroxidation end-products in Alexander's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Biopsy diagnosis of familial Alexander's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Alexander's disease: unique presentation

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Molecular findings in symptomatic and pre-symptomatic Alexander disease patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Light and electron microscopic observations on Rosenthal fibers in Alexander's disease and in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

A familial disorder associated with palatal myoclonus, other brainstem signs, tetraparesis, ataxia and Rosenthal fibre formation

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Accumulation of alpha B-crystallin in brains of patients with Alexander's disease is not due to an abnormality of the 5'-flanking and coding sequence of the genomic DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Alexander disease and intermediate filaments in astrocytes: a fatal gain of function.

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

On-grid immunogold labeling of glial intermediate filaments in epoxy-embedded tissue

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

GFAP mutations in Alexander disease

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Alexander disease: new insights from genetics

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Alexander's disease: clues to diagnosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Alexander's disease: A report and reappraisal

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

An update on the leukodsytrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Mutant NDUFV1 subunit of mitochondrial complex I causes leukodystrophy and myoclonic epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

Dysmyelinogenic leukodystrophy; report of a case of a new, presumably familial type of leukodystrophy with megalobarencephaly.

1 reference

https://api.crossref.org/works/10.1016%2FS0736-5748%2802%2900045-X

7 January 2021

10.1016/S0736-5748(02)00045-X

Identifiers

DOI

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31 July 2017

1 reference