Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature (Q31169608)

29 June 2017

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title

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

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29 June 2017

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Silvia Romano

4

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Isabella Ceccherini

object named as

Isabella Ceccherini

11

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Caterina Mariotti

3

object named as

Caterina Mariotti

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29 June 2017

Davide Pareyson

1

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29 June 2017

Roberto Fancellu

2

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29 June 2017

Andrea Salmaggi

5

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29 June 2017

Francesco Carella

6

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Floriano Girotti

7

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Grazietta Gattellaro

8

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Maria Rita Carriero

9

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Laura Farina

10

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Mario Savoiardo

12

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29 June 2017

language of work or name

English

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publication date

6 August 2008

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29 June 2017

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131

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Pt 9

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29 June 2017

2321-2331

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Mild functional effects of a novel GFAP mutant allele identified in a familial case of adult-onset Alexander disease

29 June 2017

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

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

21 January 2018

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

A novel GFAP mutation and disseminated white matter lesions: adult Alexander disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

Can MR imaging diagnose adult-onset Alexander disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

Presymptomatic testing in Huntington's disease and autosomal dominant cerebellar ataxias

21 January 2018

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

Medication use in patients with restless legs syndrome compared with a control population

21 January 2018

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

Adult-onset Alexander disease with progressive ataxia and palatal tremor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

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

21 January 2018

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

Propensity for paternal inheritance of de novo mutations in Alexander disease.

21 January 2018

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

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

21 January 2018

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

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

21 January 2018

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

Autosomal dominant palatal myoclonus and spinal cord atrophy

21 January 2018

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

GFAP and its role in Alexander disease

21 January 2018

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

Brainstem signs with progressing atrophy of medulla oblongata and upper cervical spinal cord

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

Valproate-induced parkinsonism, glial cells and Alexander's disease

21 January 2018

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

Alexander disease with hypothermia, microcoria, and psychiatric and endocrine disturbances.

21 January 2018

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

Unusual variants of Alexander's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

The functional alteration of mutant GFAP depends on the location of the domain: morphological and functional studies using astrocytoma-derived cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

Adult-onset Alexander disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWN178

21 January 2018

Identifiers

DOI

10.1093/BRAIN/AWN178

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29 June 2017

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