(Q44113919)

29 November 2017

title

Machado-Joseph disease in New England: clinical description and distinction from the olivopontocerebellar atrophies (English)

1 reference

29 November 2017

main subject

Machado-Joseph disease

1 reference

Sudarsky L

1

1 reference

29 November 2017

Corwin L

series ordinal

2

1 reference

29 November 2017

Dawson DM

series ordinal

3

1 reference

29 November 2017

language of work or name

English

0 references

publication date

1 January 1992

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29 November 2017

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29 November 2017

volume

7

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29 November 2017

issue

3

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29 November 2017

page(s)

204-208

1 reference

Machado disease: A hereditary ataxia in Portuguese emigrants to Massachusetts

29 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FMDS.870070303

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/10.1002%2FMDS.870070303

Machado-Joseph-Azorean disease. A ten-year study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FMDS.870070303

A new family with Joseph disease in Japan. Homovanillic acid, magnetic resonance, and sleep apnea studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FMDS.870070303

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/10.1002%2FMDS.870070303

21 January 2018

Identifiers

DOI

10.1002/MDS.870070303

1 reference

29 November 2017

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