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100 related items for PubMed ID: 19444286

  • 1. 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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  • 2. Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.
    Nozaki H, Ikeuchi T, Kawakami A, Kimura A, Koide R, Tsuchiya M, Nakmura Y, Mutoh T, Yamamoto H, Nakao N, Sahashi K, Nishizawa M, Onodera O.
    Mov Disord; 2007 Apr 30; 22(6):857-62. PubMed ID: 17357132
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  • 3. 16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study.
    Ouyang Y, Sakoe K, Shimazaki H, Namekawa M, Ogawa T, Ando Y, Kawakami T, Kaneko J, Hasegawa Y, Yoshizawa K, Amino T, Ishikawa K, Mizusawa H, Nakano I, Takiyama Y.
    J Neurol Sci; 2006 Sep 25; 247(2):180-6. PubMed ID: 16780885
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  • 4. Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese.
    Onodera Y, Aoki M, Mizuno H, Warita H, Shiga Y, Itoyama Y.
    Neurology; 2006 Oct 10; 67(7):1300-2. PubMed ID: 17030774
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  • 6. Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan.
    Li M, Ishikawa K, Toru S, Tomimitsu H, Takashima M, Goto J, Takiyama Y, Sasaki H, Imoto I, Inazawa J, Toda T, Kanazawa I, Mizusawa H.
    J Hum Genet; 2003 Oct 10; 48(3):111-8. PubMed ID: 12624721
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  • 7. A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan.
    Takashima M, Ishikawa K, Nagaoka U, Shoji S, Mizusawa H.
    J Hum Genet; 2001 Oct 10; 46(4):167-71. PubMed ID: 11322654
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  • 8. Severity and progression rate of cerebellar ataxia in 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA) in the endemic Nagano Area of Japan.
    Yoshida K, Shimizu Y, Morita H, Okano T, Sakai H, Ohata T, Matsumoto N, Nakamura K, Tazawa K, Ohara S, Tabata K, Inoue A, Sato S, Shimojima Y, Hattori T, Ushiyama M, Ikeda S.
    Cerebellum; 2009 Mar 10; 8(1):46-51. PubMed ID: 18855094
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  • 10. 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 Mar 10; 52(8):643-649. PubMed ID: 17611710
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  • 13. [Autosomal dominant cortical cerebellar atrophy (ADCCA) linked to chromosome 16q].
    Ishikawa K.
    Rinsho Shinkeigaku; 2001 Dec 10; 41(12):1117-9. PubMed ID: 12235813
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  • 14. Severe symptoms of 16q-ADCA coexisting with SCA8 repeat expansion.
    Ohnari K, Aoki M, Uozumi T, Tsuji S.
    J Neurol Sci; 2008 Oct 15; 273(1-2):15-8. PubMed ID: 18684474
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  • 18. Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.
    Sato K, Yabe I, Fukuda Y, Soma H, Nakahara Y, Tsuji S, Sasaki H.
    Arch Neurol; 2010 Oct 15; 67(10):1257-62. PubMed ID: 20937954
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  • 20. 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.
    J Hum Genet; 2007 Oct 15; 52(10):848-855. PubMed ID: 17805477
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