(Q48147320)

9 February 2018

title

Autosomal dominant juvenile amyotrophic lateral sclerosis. (English)

1 reference

9 February 2018

juvenile amyotrophic lateral sclerosis

main subject

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amyotrophic lateral sclerosis

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Rabin BA

1

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9 February 2018

Griffin JW

2

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9 February 2018

Crain BJ

3

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9 February 2018

Scavina M

4

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9 February 2018

Chance PF

5

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9 February 2018

Cornblath DR

6

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9 February 2018

language of work or name

English

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publication date

1 August 1999

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9 February 2018

published in

Brain

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9 February 2018

volume

122 ( Pt 8)

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9 February 2018

page(s)

1539-1550

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9 February 2018

Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Neuropathological changes in two lines of mice carrying a transgene for mutant human Cu,Zn SOD, and in mice overexpressing wild type human SOD: a model of familial amyotrophic lateral sclerosis (FALS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

An inherited disease similar to amyotrophic lateral sclerosis with a pattern of posterior column involvement. An intermediate form?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Hereditary spastic paraplegia with amyotrophy and pes cavus

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Peroneal muscular atrophy with pyramidal features

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Familial amyotrophic lateral sclerosis. A subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Epidemiologic investigations of amyotrophic lateral sclerosis. 2. Familial aggregations indicative of dominant inheritance. I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

NERVE CONDUCTION AND OTHER STUDIES IN FAMILIES WITH CHARCOT-MARIE-TOOTH DISEASE

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Molecular genetic basis of familial ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Familial amyotrophic lateral sclerosis with a mutation in the Cu/Zn superoxide dismutase gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Distal amyotrophy of predominantly the upper limbs with pyramidal features in a large kinship

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvement.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2F122.8.1539

21 January 2018

Identifiers

DOI

10.1093/BRAIN/122.8.1539

1 reference

9 February 2018

1 reference

9 February 2018