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ataxie spinocerebelárne

  1. Subject h.ataxie spinocerebelárne
    Subject h.Spinocerebellar Ataxias
    Entry termsataxia spinocerebelárna, typ 1
    ataxia spinocerebelárna, typ 2
    ataxia spinocerebelárna, typ 4
    ataxia spinocerebelárna, typ 5
    ataxia spinocerebelárna, typ 6
    ataxia spinocerebelárna, typ 7
    atrofie spinocerebelárne
    English X referencesSpinocerebellar Ataxia Type 1
    Spinocerebellar Ataxia Type 2
    Spinocerebellar Ataxia Type 4
    Spinocerebellar Ataxia Type 5
    Spinocerebellar Ataxia Type 6
    Spinocerebellar Ataxia Type 7
    Spinocerebellar Atrophies
    Scope note in EnglishA group of predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
    See also reference (FX) in Slovak ataxín-1
    ataxín-2
    ataxín-3
    ataxín-7
    ataxíny
    See also reference (FX) in English Ataxin-1
    Ataxin-2
    Ataxin-3
    Ataxin-7
    Ataxins
    Links (12) - ARTICLES
    (5) - MeSH descriptor
    (1) - BOOKS
    subject heading

    subject heading

Number of the records: 1  

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