(Q47830573)

English

Hereditary motor and sensory neuropathy associated with cerebellar atrophy (HMSNCA): clinical and neuropathological features of a Japanese family.

scientific article published in June 1998

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

Hereditary motor and sensory neuropathy associated with cerebellar atrophy (HMSNCA): clinical and neuropathological features of a Japanese family. (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

hereditary motor and sensory neuropathy

0 references

author name string

Sekijima Y

1

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

Ohara S

2

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

Nakagawa S

3

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

Tabata K

4

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

Yoshida K

5

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

Ishigame H

6

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

Shimizu Y

7

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

Yanagisawa N

8

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

publication date

1 June 1998

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

Journal of the Neurological Sciences

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

158

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

1

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

30-37

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900103-8

7 January 2021

Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900103-8

7 January 2021

Hereditary motor and sensory neuropathy associated with cerebellar atrophy (HMSNCA): a new disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900103-8

7 January 2021

Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900103-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900103-8

7 January 2021

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900103-8

7 January 2021

The neuropathology of "typical" Friedreich's ataxia in Quebec.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900103-8

7 January 2021

Hereditary ataxia with sensory neuronopathy: Biemond's ataxia.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900103-8

7 January 2021

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900103-8

7 January 2021

Brain Lesions in Friedreich's Ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900103-8

7 January 2021

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900103-8

7 January 2021

Identifiers

10.1016/S0022-510X(98)00103-8

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9667774

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