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333 related items for PubMed ID: 17661799

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 4. A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.
    Owada K, Ishikawa K, Toru S, Ishida G, Gomyoda M, Tao O, Noguchi Y, Kitamura K, Kondo I, Noguchi E, Arinami T, Mizusawa H.
    Neurology; 2005 Aug 23; 65(4):629-32. PubMed ID: 16116133
    [Abstract] [Full Text] [Related]

  • 5. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
    Waters MF, Fee D, Figueroa KP, Nolte D, Müller U, Advincula J, Coon H, Evidente VG, Pulst SM.
    Neurology; 2005 Oct 11; 65(7):1111-3. PubMed ID: 16135769
    [Abstract] [Full Text] [Related]

  • 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 11; 54(7):377-81. PubMed ID: 19444286
    [Abstract] [Full Text] [Related]

  • 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 11; 48(3):111-8. PubMed ID: 12624721
    [Abstract] [Full Text] [Related]

  • 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 11; 8(1):46-51. PubMed ID: 18855094
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. 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 Apr 30; 46(4):167-71. PubMed ID: 11322654
    [Abstract] [Full Text] [Related]

  • 11. Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis.
    Infante J, Combarros O, Volpini V, Corral J, Llorca J, Berciano J.
    Acta Neurol Scand; 2005 Jun 30; 111(6):391-9. PubMed ID: 15876341
    [Abstract] [Full Text] [Related]

  • 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 30; 5(4):215-21. PubMed ID: 15455264
    [Abstract] [Full Text] [Related]

  • 13. Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I.
    Benomar A, Le Guern E, Dürr A, Ouhabi H, Stevanin G, Yahyaoui M, Chkili T, Agid Y, Brice A.
    Ann Neurol; 1994 Apr 30; 35(4):439-44. PubMed ID: 8154871
    [Abstract] [Full Text] [Related]

  • 14. Prevalence of spinocerebellar degenerations in the Hokuriku district in Japan.
    Shibata-Hamaguchi A, Ishida C, Iwasa K, Yamada M.
    Neuroepidemiology; 2009 Apr 30; 32(3):176-83. PubMed ID: 19169038
    [Abstract] [Full Text] [Related]

  • 15. Genetic heterogeneity of autosomal dominant nonprogressive congenital ataxia.
    Jen JC, Lee H, Cha YH, Nelson SF, Baloh RW.
    Neurology; 2006 Nov 14; 67(9):1704-6. PubMed ID: 17101914
    [Abstract] [Full Text] [Related]

  • 16. Cerebellar ataxia with spasmodic cough: a new form of dominant ataxia.
    Coutinho P, Cruz VT, Tuna A, Silva SE, Guimarães J.
    Arch Neurol; 2006 Apr 14; 63(4):553-5. PubMed ID: 16606768
    [Abstract] [Full Text] [Related]

  • 17. 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 14; 67(10):1257-62. PubMed ID: 20937954
    [Abstract] [Full Text] [Related]

  • 18. 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 Oct 14; 51(5):461-466. PubMed ID: 16614795
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. [Autosomal dominant cerebellar ataxias in the Netherlands: a national inventory].
    van de Warrenburg BP.
    Ned Tijdschr Geneeskd; 2001 May 19; 145(20):962-7. PubMed ID: 11396263
    [Abstract] [Full Text] [Related]

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