(Q41364983)

29 September 2017

1 reference

title

Clinicopathology of spinocerebellar degeneration: its correlation to the unstable CAG repeat of the affected gene (English)

1 reference

29 September 2017

Yagishita S

1

1 reference

PubMed ID

9051687

29 September 2017

Inoue M

series ordinal

2

1 reference

PubMed ID

9051687

29 September 2017

language of work or name

1 reference

1 January 1997

1 reference

29 September 2017

Pathology International

1 reference

29 September 2017

47

1 reference

29 September 2017

1

1 reference

29 September 2017

1-15

1 reference

Machado disease: A hereditary ataxia in Portuguese emigrants to Massachusetts

29 September 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1827.1997.TB04429.X

Autosomal dominant striatonigral degeneration. A clinical, pathologic, and biochemical study of a new genetic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1827.1997.TB04429.X

Family with dominantly inherited ataxia, amyotrophy, and peripheral sensory loss. Spinopontine atrophy or Machado-Joseph Azorean disease in another non-Portuguese family?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1827.1997.TB04429.X

Autosomal dominant system degeneration in Portuguese families of the Azores Islands. A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1827.1997.TB04429.X

Analysis of spinocerebellar ataxia type 1 (SCA1)-related CAG trinucleotide expansion in Japan

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1827.1997.TB04429.X

Olivopontocerebellar degeneration. Clinical and ultrastructural abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1827.1997.TB04429.X

Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1827.1997.TB04429.X

Familial chorea and myoclonus epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1827.1997.TB04429.X

A neurological syndrome associated with orthostatic hypotension: a clinical-pathologic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1827.1997.TB04429.X

Olivopontocerebellar atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1827.1997.TB04429.X

Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1827.1997.TB04429.X

10.1111/J.1440-1827.1997.TB04429.X

21 January 2018

Identifiers

DOI

1 reference

29 September 2017

1 reference

PubMed ID

9051687