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Journal Abstract Search

285 related items for PubMed ID: 17030774

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  • 3. Clinical and genetic epidemiological study of 16q22.1-linked autosomal dominant cerebellar ataxia in western Japan.
    Hayashi M, Adachi Y, Mori M, Nakano T, Nakashima K.
    Acta Neurol Scand; 2007 Aug; 116(2):123-7. PubMed ID: 17661799
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  • 6. Clinical and genetic characterization of 16q-linked autosomal dominant spinocerebellar ataxia in South Kyushu, Japan.
    Hirano R, Takashima H, Okubo R, Okamoto Y, Maki Y, Ishida S, Suehara M, Hokezu Y, Arimura K.
    J Hum Genet; 2009 Jul; 54(7):377-81. PubMed ID: 19444286
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  • 8. Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia.
    Amino T, Ishikawa K, Toru S, Ishiguro T, Sato N, Tsunemi T, Murata M, Kobayashi K, Inazawa J, Toda T, Mizusawa H.
    J Hum Genet; 2007 Jul; 52(8):643-649. PubMed ID: 17611710
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  • 12. Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.
    Hirano R, Takashima H, Okubo R, Tajima K, Okamoto Y, Ishida S, Tsuruta K, Arisato T, Arata H, Nakagawa M, Osame M, Arimura K.
    Neurogenetics; 2004 Dec; 5(4):215-21. PubMed ID: 15455264
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  • 16. A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxia.
    Nagaoka U, Takashima M, Ishikawa K, Yoshizawa K, Yoshizawa T, Ishikawa M, Yamawaki T, Shoji S, Mizusawa H.
    Neurology; 2000 May 23; 54(10):1971-5. PubMed ID: 10822439
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