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Journal Abstract Search

285 related items for PubMed ID: 17030774

  • 1. 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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  • 2. 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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  • 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 25; 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 25; 54(7):377-81. PubMed ID: 19444286
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  • 7. 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 Jul 25; 48(3):111-8. PubMed ID: 12624721
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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 25; 5(4):215-21. PubMed ID: 15455264
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  • 14. A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano.
    Ohata T, Yoshida K, Sakai H, Hamanoue H, Mizuguchi T, Shimizu Y, Okano T, Takada F, Ishikawa K, Mizusawa H, Yoshiura KI, Fukushima Y, Ikeda SI, Matsumoto N.
    J Hum Genet; 2006 Dec 25; 51(5):461-466. PubMed ID: 16614795
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  • 15. [Autosomal dominant cortical cerebellar atrophy (ADCCA) linked to chromosome 16q].
    Ishikawa K.
    Rinsho Shinkeigaku; 2001 Dec 25; 41(12):1117-9. PubMed ID: 12235813
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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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  • 20. 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 23; 67(10):1257-62. PubMed ID: 20937954
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