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Psychosis in spinocerebellar ataxias: a case series and study of tyrosine hydroxylase in substantia nigra

Spinocerebellar ataxias are a genetically heterogeneous group of degenerative diseases typically characterized by progressive ataxia and to various degrees, neuropathy, amyotrophy, and ocular abnormalities. There is increasing evidence for non-motor manifestations associated with cerebellar syndrome...

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Podrobná bibliografie
Vydáno v:Cerebellum
Hlavní autoři: Turk, Katherine W, Flanagan, Margaret E, Josephson, Samuel, Keene, C Dirk, Jayadev, Suman, Bird, Thomas D
Médium: Artigo
Jazyk:Inglês
Vydáno: 2018
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5843512/
https://ncbi.nlm.nih.gov/pubmed/28887803
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12311-017-0882-5
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