(Q28237850)

English

A large kindred with autosomal dominant Parkinson's disease

scientific article (publication date: March 1990)

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title

A large kindred with autosomal dominant Parkinson's disease (English)

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L I Golbe

1

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G Di Iorio

series ordinal

2

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V Bonavita

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3

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D C Miller

series ordinal

4

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R C Duvoisin

series ordinal

5

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language of work or name

English

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publication date

March 1990

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published in

Annals of Neurology

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volume

27

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page(s)

276-82

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issue

3

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cites work

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

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reference URL

https://api.crossref.org/works/10.1002%2FANA.410270309

retrieved

21 January 2018

Hereditary Mental Depression and Parkinsonism With Taurine Deficiency

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.410270309

retrieved

21 January 2018

Joseph disease: a multisystem degenerative disorder of the nervous system

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stated in

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reference URL

https://api.crossref.org/works/10.1002%2FANA.410270309

retrieved

21 January 2018

Neuropathologic changes in ataxia-telangiectasia

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reference URL

https://api.crossref.org/works/10.1002%2FANA.410270309

retrieved

21 January 2018

Familial amyotrophic lateral sclerosis. A subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.410270309

retrieved

21 January 2018

Hereditary amyotrophic lateral sclerosis. Histochemical and electron microscopic study of hyaline inclusions in motor neurons

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.410270309

retrieved

21 January 2018

Case-control study of early life dietary factors in Parkinson's disease

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stated in

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reference URL

https://api.crossref.org/works/10.1002%2FANA.410270309

retrieved

21 January 2018

Identifiers

DOI

10.1002/ANA.410270309

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PubMed ID

2158268

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(Q28237850)

A large kindred with autosomal dominant Parkinson's disease

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