(Q30676384)

26 June 2017

title

Autosomal dominant palatal myoclonus and spinal cord atrophy (English)

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26 June 2017

Yuji Okamoto

1

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26 June 2017

Hideo Mitsuyama

2

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26 June 2017

Manabu Jonosono

3

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26 June 2017

Keiko Hirata

4

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26 June 2017

Kimiyoshi Arimura

5

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26 June 2017

Mitsuhiro Osame

6

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26 June 2017

Masanori Nakagawa

7

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26 June 2017

publication date

1 March 2002

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Journal of the Neurological Sciences

26 June 2017

published in

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26 June 2017

volume

195

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26 June 2017

issue

1

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26 June 2017

page(s)

71-76

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Symptomatic and essential rhythmic palatal myoclonus.

26 June 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

Hereditary branchial myoclonus with spastic paraparesis and cerebellar ataxia: A new autosomal dominant disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

Palatal tremor, progressive multiple cranial nerve palsies, and cerebellar ataxia: a case report and review of literature of palatal tremors in neurodegenerative disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

Clinical phenotype in X-linked Charcot-Marie-Tooth disease with an entire deletion of the connexin 32 coding sequence

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

Prevalence of triplet repeat expansion in ataxia patients from Hokkaido, the northernmost island of Japan

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

Characterization of human cDNA and genomic clones for glial fibrillary acidic protein.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

Alexander's disease: A report and reappraisal

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

Alexander's disease. A disease of astrocytes.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

Alexander disease--classification revisited and isolation of a neonatal form

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900687-6

10.1016/S0022-510X(01)00687-6

7 January 2021

Identifiers

DOI

1 reference

26 June 2017

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