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Journal Abstract Search

356 related items for PubMed ID: 18627481

  • 1. Chromosome 16q22.1-linked autosomal dominant cerebellar ataxia: an autopsy case report with some new observations on cerebellar pathology.
    Shintaku M, Kaneda D.
    Neuropathology; 2009 Jun; 29(3):285-92. PubMed ID: 18627481
    [Abstract] [Full Text] [Related]

  • 2. The chromosome 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell: The 50th Anniversary of Japanese Society of Neuropathology.
    Ishikawa K, Mizusawa H.
    Neuropathology; 2010 Oct; 30(5):490-4. PubMed ID: 20667009
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  • 3. 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
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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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  • 5. Mesenchymal stem cells rescue Purkinje cells and improve motor functions in a mouse model of cerebellar ataxia.
    Jones J, Jaramillo-Merchán J, Bueno C, Pastor D, Viso-León M, Martínez S.
    Neurobiol Dis; 2010 Nov 10; 40(2):415-23. PubMed ID: 20638477
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  • 6. 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 10; 116(2):123-7. PubMed ID: 17661799
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  • 7. The toppler mouse: a novel mutant exhibiting loss of Purkinje cells.
    Duchala CS, Shick HE, Garcia J, Deweese DM, Sun X, Stewart VJ, Macklin WB.
    J Comp Neurol; 2004 Aug 16; 476(2):113-29. PubMed ID: 15248193
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  • 8. Sequence of cellular events in cerebellar ontogeny relevant to expression of neuronal abnormalities in ataxia-telangiectasia.
    Vinters HV, Gatti RA, Rakic P.
    Kroc Found Ser; 1985 Aug 16; 19():233-55. PubMed ID: 3864938
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  • 10. On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA.
    Ishikawa K, Mizusawa H.
    Neuropathology; 2006 Aug 16; 26(4):352-60. PubMed ID: 16961073
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  • 11. An autopsy case of spinocerebellar ataxia type 6 with mental symptoms of schizophrenia and dementia.
    Tashiro H, Suzuki SO, Hitotsumatsu T, Iwaki T.
    Clin Neuropathol; 1999 Aug 16; 18(4):198-204. PubMed ID: 10442462
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  • 12. Moderate loss of cerebellar Purkinje cells after chronic bilateral common carotid artery occlusion in rats.
    Kántor O, Schmitz C, Feiser J, Brasnjevic I, Korr H, Busto R, Ginsberg MD, Schmidt-Kastner R.
    Acta Neuropathol; 2007 May 16; 113(5):549-58. PubMed ID: 17308915
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  • 16. Preliminary characterization of hereditary cerebellar ataxia in rats.
    La Regina MC, Yates-Siilata K, Woods L, Tolbert D.
    Lab Anim Sci; 1992 Feb 16; 42(1):19-26. PubMed ID: 1316503
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  • 17. Canine inherited ataxia.
    Cork LC, Troncoso JC, Price DL.
    Ann Neurol; 1981 May 16; 9(5):492-8. PubMed ID: 7271243
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  • 18. [Cerebellar cortical degeneration in an American Staffordshire terrier].
    Buijtels JJ, Kroeze EJ, Voorhout G, Schellens CJ, van Nes JJ.
    Tijdschr Diergeneeskd; 1981 May 16; 131(14-15):518-22. PubMed ID: 16916197
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