(Q28507600)

24 January 2017

title

Genetic and age related models of neurodegeneration in mice: dystrophic axons (English)

1 reference

ATPase, aminophospholipid transporter-like, class I, type 8A, member 2

24 January 2017

main subject

1 reference

GOA release 2020-03-11

Dystonin

1 reference

GOA release 2020-03-11

1 reference

R. T. Bronson

1

1 reference

24 January 2017

H. O. Sweet

series ordinal

2

1 reference

24 January 2017

C. A. Spencer

series ordinal

3

1 reference

24 January 2017

M. T. Davisson

series ordinal

4

1 reference

24 January 2017

publication date

1 May 1992

1 reference

24 January 2017

published in

Journal of Neurogenetics

1 reference

24 January 2017

volume

8

1 reference

24 January 2017

issue

2

1 reference

24 January 2017

page(s)

71–83

1 reference

Axonal dystrophy in the gracile nucleus of man

24 January 2017

cites work

1 reference

https://api.crossref.org/works/10.3109%2F01677069209084153

Systemic neuroaxonal dystrophy in Suffolk sheep.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01677069209084153

CLINICAL AND PATHOLOGICAL STUDIES OF AN HEREDITARY NEUROPATHY IN MICE (DYSTONIA MUSCULORUM)

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01677069209084153

Cerebellar alterations in the weaver mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01677069209084153

Infantile neuroaxonal dystrophy and its relationship to Hallervorden-Spatz disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01677069209084153

Ultrastructural studies of an hereditary sensory neuropathy in mice (dystonia musculorum)

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01677069209084153

Scrapie as a model for neuroaxonal dystrophy: ultrastructural studies

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01677069209084153

Neuroaxonal dystrophy in childhood. Report of two second cousins with Hallerworden-Spatz disease, and a case of Seitelberger's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01677069209084153

Pathological Findings in Shambling, A Hereditary Neuropathy of Mice*†

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01677069209084153

Infantile neuroaxonal dystrophy: perinatal onset with symptoms of diencephalic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01677069209084153

Stargazer: a new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01677069209084153

Infantile neuroaxonal dystrophy: cortical axonic and presynaptic changes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01677069209084153

Gracile axonal dystrophy (GAD), a new neurological mutant in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F01677069209084153

10.3109/01677069209084153

21 January 2018

Identifiers

DOI

0 references

1 reference