(Q49096728)

English

Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-I, Machado-Joseph disease, or Dentato-Rubro-Pallido-Luysian atrophy locus.

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scholarly article

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/8684388

Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-I, Machado-Joseph disease, or Dentato-Rubro-Pallido-Luysian atrophy locus. (English)

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/8684388

Machado-Joseph disease

1 reference

based on heuristic

inferred from title

author name string

Subramony SH

1

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/8684388

Fratkin JD

2

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/8684388

Manyam BV

3

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/8684388

Currier RD

4

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/8684388

language of work or name

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publication date

1 March 1996

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/8684388

Movement Disorders

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/8684388

11

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/8684388

2

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/8684388

174-180

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/8684388

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

1 reference

https://api.crossref.org/works/10.1002%2FMDS.870110210

21 January 2018

Dominant spinopontine atrophy. Report of two additional members of family W

1 reference

https://api.crossref.org/works/10.1002%2FMDS.870110210

21 January 2018

Morphometric studies in dominant olivopontocerebellar atrophy. Comparison of cell losses with amino acid decreases

1 reference

https://api.crossref.org/works/10.1002%2FMDS.870110210

21 January 2018

Joseph disease: a multisystem degenerative disorder of the nervous system

1 reference

https://api.crossref.org/works/10.1002%2FMDS.870110210

21 January 2018

Identifiers

10.1002/MDS.870110210

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/8684388

1 reference

Europe PubMed Central

18 February 2018

http://europepmc.org/abstract/MED/8684388

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