(Q47615896)

4 February 2018

title

Alexander disease: a leukodystrophy caused by a mutation in GFAP. (English)

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4 February 2018

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Anne B Johnson

1

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4 February 2018

publication date

1 May 2004

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4 February 2018

published in

Neurochemical Research

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4 February 2018

volume

29

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4 February 2018

issue

5

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4 February 2018

page(s)

961-964

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4 February 2018

https://scigraph.springernature.com/pub.10.1023/b:nere.0000021240.30518.2c

exact match

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cites work

GFAP mutations in Alexander disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Alexander's disease: clinical, pathologic, and genetic features

1 reference

12 December 2020

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

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12 December 2020

Alexander disease: new insights from genetics

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12 December 2020

GFAP: functional implications gleaned from studies of genetically engineered mice

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12 December 2020

Targeted deletion in astrocyte intermediate filament (Gfap) alters neuronal physiology

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12 December 2020

Mutations associated with a childhood leukodystrophy, Alexander disease, cause deficiency in dimerization of the cytoskeletal protein GFAP

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12 December 2020

Alexander's disease: unique presentation

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12 December 2020

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

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12 December 2020

Electron microscopic and neurochemical study of Alexander's disease (author's transl)

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12 December 2020

Rosenthal fibers share epitopes with alpha B-crystallin, glial fibrillary acidic protein, and ubiquitin, but not with vimentin. Immunoelectron microscopy with colloidal gold

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12 December 2020

Atypical focal MRI lesions in a case of juvenile Alexander's disease

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12 December 2020

Fluctuation of computed tomographic findings in white matter in Alexander's disease

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12 December 2020

Overexpression and abnormal modification of the stress proteins alpha B-crystallin and HSP27 in Alexander disease

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12 December 2020

Alpha B-crystallin is expressed in non-lenticular tissues and accumulates in Alexander's disease brain

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Advanced glycation modification of Rosenthal fibers in patients with Alexander disease

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12 December 2020

Autosomal dominant palatal myoclonus and spinal cord atrophy

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12 December 2020

Alexander disease: a review and the gene

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12 December 2020

Fatal encephalopathy with astrocyte inclusions in GFAP transgenic mice

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12 December 2020

Alexander's disease in adults and diffuse cerebral gliomatosis in 2 members of the same family

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12 December 2020

Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L.

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12 December 2020

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

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12 December 2020

Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patients

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12 December 2020

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

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12 December 2020

Molecular findings in symptomatic and pre-symptomatic Alexander disease patients

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12 December 2020

Hereditary adult-onset Alexander's disease with palatal myoclonus, spastic paraparesis, and cerebellar ataxia

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12 December 2020

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

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12 December 2020

GFAP is necessary for the integrity of CNS white matter architecture and long-term maintenance of myelination

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12 December 2020

Alexander disease: diagnosis with MR imaging.

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12 December 2020

Diffuse Rosenthal Fiber Formation in the Adult: A Report of Four Cases

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12 December 2020

Alexander's disease. A disease of astrocytes

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12 December 2020

Alexander's disease: clues to diagnosis.

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12 December 2020

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

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12 December 2020

Advanced lipid peroxidation end-products in Alexander's disease

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12 December 2020

Alexander's disease: A report and reappraisal

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12 December 2020

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

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12 December 2020

10.1023/B:NERE.0000021240.30518.2C

Identifiers

DOI

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4 February 2018

Dimensions Publication ID

1027379964

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1 reference

4 February 2018