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312 related items for PubMed ID: 17357132

  • 21. 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; 48(3):111-8. PubMed ID: 12624721
    [Abstract] [Full Text] [Related]

  • 22. Cognitive impairment in SCA-19.
    Schelhaas HJ, van de Warrenburg BP, Hageman G, Ippel EE, van Hout M, Kremer B.
    Acta Neurol Belg; 2003 Dec; 103(4):199-205. PubMed ID: 15008504
    [Abstract] [Full Text] [Related]

  • 23. Spinocerebellar ataxia type 15: diagnostic assessment, frequency, and phenotypic features.
    Synofzik M, Beetz C, Bauer C, Bonin M, Sanchez-Ferrero E, Schmitz-Hübsch T, Wüllner U, Nägele T, Riess O, Schöls L, Bauer P.
    J Med Genet; 2011 Jun; 48(6):407-12. PubMed ID: 21367767
    [Abstract] [Full Text] [Related]

  • 24. 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 Jun; 52(10):848-855. PubMed ID: 17805477
    [Abstract] [Full Text] [Related]

  • 25. [Autosomal dominant cortical cerebellar atrophy (ADCCA) linked to chromosome 16q].
    Ishikawa K.
    Rinsho Shinkeigaku; 2001 Dec; 41(12):1117-9. PubMed ID: 12235813
    [Abstract] [Full Text] [Related]

  • 26. Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15.
    Weissbach A, Djarmati A, Klein C, Dragasević N, Zühlke C, Raković A, Guzvić M, Butz E, Tönnies H, Siebert R, Petrović I, Svetel M, Kostić VS, Lohmann K.
    Mov Disord; 2010 Aug 15; 25(11):1577-82. PubMed ID: 20589871
    [Abstract] [Full Text] [Related]

  • 27. New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14.
    Klebe S, Durr A, Rentschler A, Hahn-Barma V, Abele M, Bouslam N, Schöls L, Jedynak P, Forlani S, Denis E, Dussert C, Agid Y, Bauer P, Globas C, Wüllner U, Brice A, Riess O, Stevanin G.
    Ann Neurol; 2005 Nov 15; 58(5):720-9. PubMed ID: 16193476
    [Abstract] [Full Text] [Related]

  • 28. Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3.
    Verbeek DS, van de Warrenburg BP, Wesseling P, Pearson PL, Kremer HP, Sinke RJ.
    Brain; 2004 Nov 15; 127(Pt 11):2551-7. PubMed ID: 15306549
    [Abstract] [Full Text] [Related]

  • 29. 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 Nov 15; 52(8):643-649. PubMed ID: 17611710
    [Abstract] [Full Text] [Related]

  • 30. Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients.
    Dragasević NT, Culjković B, Klein C, Ristić A, Keckarević M, Topisirović I, Vukosavić S, Svetel M, Kock N, Stefanova E, Romac S, Kostić VS.
    Mov Disord; 2006 Feb 15; 21(2):187-91. PubMed ID: 16149098
    [Abstract] [Full Text] [Related]

  • 31. Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
    Jiang H, Tang BS, Xu B, Zhao GH, Shen L, Tang JG, Li QH, Xia K.
    Chin Med J (Engl); 2005 May 20; 118(10):837-43. PubMed ID: 15989765
    [Abstract] [Full Text] [Related]

  • 32. The CNTN4 c.4256C>T mutation is rare in Japanese with inherited spinocerebellar ataxia.
    Tanaka E, Maruyama H, Morino H, Nakajima E, Kawakami H.
    J Neurol Sci; 2008 Mar 15; 266(1-2):180-1. PubMed ID: 17915252
    [Abstract] [Full Text] [Related]

  • 33. Mutational screening of 320 Brazilian patients with autosomal dominant spinocerebellar ataxia.
    Cintra VP, Lourenço CM, Marques SE, de Oliveira LM, Tumas V, Marques W.
    J Neurol Sci; 2014 Dec 15; 347(1-2):375-9. PubMed ID: 25466696
    [Abstract] [Full Text] [Related]

  • 34. Spinocerebellar ataxias.
    Teive HA.
    Arq Neuropsiquiatr; 2009 Dec 15; 67(4):1133-42. PubMed ID: 20069236
    [Abstract] [Full Text] [Related]

  • 35. [Spinocerebellar ataxia 1--clinical study of 17 patients in a large pedigree].
    Sasaki H, Wakisaka A, Koyama T, Hamada T, Shima K, Tashiro K, Hashimoto K, Miyagishi T.
    No To Shinkei; 1993 Jun 15; 45(6):502-8. PubMed ID: 8363844
    [Abstract] [Full Text] [Related]

  • 36. Clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypes.
    Maschke M, Oehlert G, Xie TD, Perlman S, Subramony SH, Kumar N, Ptacek LJ, Gomez CM.
    Mov Disord; 2005 Nov 15; 20(11):1405-12. PubMed ID: 16037936
    [Abstract] [Full Text] [Related]

  • 37. Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families.
    Jiang H, Tang B, Xia K, Zhou Y, Xu B, Zhao G, Li H, Shen L, Pan Q, Cai F.
    J Neurol Sci; 2005 Sep 15; 236(1-2):25-9. PubMed ID: 15979648
    [Abstract] [Full Text] [Related]

  • 38. 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 15; 5(4):215-21. PubMed ID: 15455264
    [Abstract] [Full Text] [Related]

  • 39. 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 Dec 15; 46(4):167-71. PubMed ID: 11322654
    [Abstract] [Full Text] [Related]

  • 40. [Molecular genetics and its clinical application in the diagnosis of spinocerebellar ataxias].
    Xie QY, Liang XL, Li XH.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb 15; 22(1):71-3. PubMed ID: 15696485
    [Abstract] [Full Text] [Related]

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