(Q48453426)

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Cognitive impairment in families with pure autosomal dominant hereditary spastic paraparesis

scientific article published in May 1998

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Europe PubMed Central

PubMed publication ID

9619194

retrieved

11 February 2018

reference URL

http://europepmc.org/abstract/MED/9619194

title

Cognitive impairment in families with pure autosomal dominant hereditary spastic paraparesis (English)

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Europe PubMed Central

PubMed publication ID

9619194

retrieved

11 February 2018

reference URL

http://europepmc.org/abstract/MED/9619194

main subject

cognitive dysfunction

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2

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Europe PubMed Central

PubMed publication ID

9619194

retrieved

11 February 2018

reference URL

http://europepmc.org/abstract/MED/9619194

author name string

Webb S

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1

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Europe PubMed Central

PubMed publication ID

9619194

retrieved

11 February 2018

reference URL

http://europepmc.org/abstract/MED/9619194

language of work or name

English

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publication date

1 May 1998

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Europe PubMed Central

PubMed publication ID

9619194

retrieved

11 February 2018

reference URL

http://europepmc.org/abstract/MED/9619194

published in

Brain

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Europe PubMed Central

PubMed publication ID

9619194

retrieved

11 February 2018

reference URL

http://europepmc.org/abstract/MED/9619194

volume

121 ( Pt 5)

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Europe PubMed Central

PubMed publication ID

9619194

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11 February 2018

reference URL

http://europepmc.org/abstract/MED/9619194

page(s)

923-929

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Europe PubMed Central

PubMed publication ID

9619194

retrieved

11 February 2018

reference URL

http://europepmc.org/abstract/MED/9619194

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DOI

10.1093/BRAIN/121.5.923

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stated in

Europe PubMed Central

PubMed publication ID

9619194

retrieved

11 February 2018

reference URL

http://europepmc.org/abstract/MED/9619194

PubMed publication ID

9619194

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9619194

retrieved

11 February 2018

reference URL

http://europepmc.org/abstract/MED/9619194

ResearchGate publication ID

13665677

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(Q48453426)

Cognitive impairment in families with pure autosomal dominant hereditary spastic paraparesis

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