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Neuroepidemiology
Volumn 32, Issue 3, 2009, Pages 184-185
Spinocerebellar degenerations in Japan: New insights from an epidemiological study
Author keywords

[No Author keywords available]
Indexed keywords

AUTOSOMAL DOMINANT DISORDER; CEREBELLAR ATAXIA; HUMAN; JAPAN; MACHADO JOSEPH DISEASE; MORBIDITY; NOTE; PREVALENCE; SPINOCEREBELLAR DEGENERATION;
EID: 58349091920     PISSN: 02515350     EISSN: None     Source Type: Journal    
DOI: 10.1159/000195687     Document Type: Note
Times cited : (13)
References (14)
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  • 2
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  • 4
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    • Idiopathic' late onset cerebellar ataxia: A clinical and genetic study of 36 cases
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    • Harding, A.E.1
  • 5
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    • Pure cerebello-olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline and chorea
    • Fox SH, Nieves A, Bergeron C, Lang AE: Pure cerebello-olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline and chorea. Mov Disord 2003;18:1550-1554.
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  • 6
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    • The hereditary spinocerebellar ataxias in Japan
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  • 8
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    • Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: A study of 113 Japanese families
    • Basri R, Yabe I, Soma H, Sasaki H: Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families. J Hum Genet 2007;52:848-855.
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  • 9
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  • 10
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  • 11
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  • 12
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.