Prominent sensory and autonomic disturbances in familial amyotrophic lateral sclerosis with a Gly93Ser mutation in the SOD1 gene (Q74142838)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9455983%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

Prominent sensory and autonomic disturbances in familial amyotrophic lateral sclerosis with a Gly93Ser mutation in the SOD1 gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9455983%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

9 November 2019

main subject

1 reference

A Kawata

1

1 reference

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9 November 2019

S Kato

series ordinal

2

1 reference

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9 November 2019

H Hayashi

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9455983%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

S Hirai

series ordinal

4

1 reference

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9 November 2019

publication date

1 December 1997

1 reference

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Journal of the Neurological Sciences

9 November 2019

published in

1 reference

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9 November 2019

volume

153

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9 November 2019

issue

1

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9 November 2019

page(s)

82-85

1 reference

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Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: a possible new subtype of familial ALS

9 November 2019

cites work

1 reference

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Variance of age at onset in a Japanese family with amyotrophic lateral sclerosis associated with a novel Cu/Zn superoxide dismutase mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2900176-7

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2900176-7

Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2900176-7

Identification of two novel mutations and a new polymorphism in the gene for Cu/Zn superoxide dismutase in patients with amyotrophic lateral sclerosis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2900176-7

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2900176-7

Architecture and anatomy of the chromosomal locus in human chromosome 21 encoding the Cu/Zn superoxide dismutase.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2900176-7

Familial adult motor neuron disease: amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2900176-7

Reevaluation of assay methods and establishment of kit for superoxide dismutase activity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2900176-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2900176-7

Circulatory collapse and sudden death in respirator-dependent amyotrophic lateral sclerosis.

7 January 2021

1 reference

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Genetics of amyotrophic lateral sclerosis

7 January 2021

1 reference

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Haplotype analysis of familial amyloidotic polyneuropathy

7 January 2021

1 reference

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10.1016/S0022-510X(97)00176-7

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9455983%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference