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Journal Abstract Search

793 related items for PubMed ID: 9124808

  • 1. Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1.
    Hashida H, Goto J, Kurisaki H, Mizusawa H, Kanazawa I.
    Ann Neurol; 1997 Apr; 41(4):505-11. PubMed ID: 9124808
    [Abstract] [Full Text] [Related]

  • 2. Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and Machado-Joseph disease.
    Lopes-Cendes I, Maciel P, Kish S, Gaspar C, Robitaille Y, Clark HB, Koeppen AH, Nance M, Schut L, Silveira I, Coutinho P, Sequeiros J, Rouleau GA.
    Ann Neurol; 1996 Aug; 40(2):199-206. PubMed ID: 8773601
    [Abstract] [Full Text] [Related]

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  • 4. Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph disease.
    Cancel G, Gourfinkel-An I, Stevanin G, Didierjean O, Abbas N, Hirsch E, Agid Y, Brice A.
    Hum Mutat; 1998 Aug; 11(1):23-7. PubMed ID: 9450899
    [Abstract] [Full Text] [Related]

  • 5. [Molecular basis of heterogeneities of clinical presentation of dentatorubral pallidoluysian atrophy (DRPLA)].
    Tsuji S.
    Rinsho Shinkeigaku; 1994 Dec; 34(12):1227-9. PubMed ID: 7774119
    [Abstract] [Full Text] [Related]

  • 6. Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease.
    Matilla T, McCall A, Subramony SH, Zoghbi HY.
    Ann Neurol; 1995 Jul; 38(1):68-72. PubMed ID: 7611728
    [Abstract] [Full Text] [Related]

  • 7. Mendelian segregation of normal CAG trinucleotide repeat alleles at three autosomal loci.
    MacMillan JC, Voisey J, Healey SC, Martin NG.
    J Med Genet; 1999 Mar; 36(3):258-9. PubMed ID: 10204858
    [Abstract] [Full Text] [Related]

  • 8. Molecular pathology of dentatorubral-pallidoluysian atrophy.
    Kanazawa I.
    Philos Trans R Soc Lond B Biol Sci; 1999 Jun 29; 354(1386):1069-74. PubMed ID: 10434307
    [Abstract] [Full Text] [Related]

  • 9. Dentatorubral-pallidoluysian atrophy (DRPLA). Molecular basis for wide clinical features of DRPLA.
    Ikeuchi T, Koide R, Onodera O, Tanaka H, Oyake M, Takano H, Tsuji S.
    Clin Neurosci; 1995 Jun 29; 3(1):23-7. PubMed ID: 7614090
    [Abstract] [Full Text] [Related]

  • 10. Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.
    Dürr A, Stevanin G, Cancel G, Duyckaerts C, Abbas N, Didierjean O, Chneiweiss H, Benomar A, Lyon-Caen O, Julien J, Serdaru M, Penet C, Agid Y, Brice A.
    Ann Neurol; 1996 Apr 29; 39(4):490-9. PubMed ID: 8619527
    [Abstract] [Full Text] [Related]

  • 11. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
    Oda M, Maruyama H, Komure O, Morino H, Terasawa H, Izumi Y, Imamura T, Yasuda M, Ichikawa K, Ogawa M, Matsumoto M, Kawakami H.
    Arch Neurol; 2004 Feb 29; 61(2):209-12. PubMed ID: 14967767
    [Abstract] [Full Text] [Related]

  • 12. Differential pattern in tissue-specific somatic mosaicism of expanded CAG trinucleotide repeats in dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and X-linked recessive spinal and bulbar muscular atrophy.
    Tanaka F, Sobue G, Doyu M, Ito Y, Yamamoto M, Shimada N, Yamamoto K, Riku S, Hshizume Y, Mitsuma T.
    J Neurol Sci; 1996 Jan 29; 135(1):43-50. PubMed ID: 8926495
    [Abstract] [Full Text] [Related]

  • 13. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
    Tang B, Xia J, Wang D, Tang X, Shen L, Liu C, Dai H, Yan X, Pan Q, Xiao J, Zhang B, Ou Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct 29; 16(5):281-4. PubMed ID: 10514531
    [Abstract] [Full Text] [Related]

  • 14. [Molecular and clinical features in spinocerebellar ataxia type 6 (SCA6) in Japanese].
    Ikeuchi T.
    Nihon Rinsho; 1999 Apr 29; 57(4):891-5. PubMed ID: 10222785
    [Abstract] [Full Text] [Related]

  • 15. Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat.
    Ikeuchi T, Koide R, Tanaka H, Onodera O, Igarashi S, Takahashi H, Kondo R, Ishikawa A, Tomoda A, Miike T.
    Ann Neurol; 1995 Jun 29; 37(6):769-75. PubMed ID: 7778850
    [Abstract] [Full Text] [Related]

  • 16. [A sporadic case of dentatorubral-pallidoluysian atrophy (DRPLA) having an elderly age of onset].
    Horikawa H, Futamura N, Uetakagaito M.
    Rinsho Shinkeigaku; 1996 Apr 29; 36(4):584-6. PubMed ID: 8810854
    [Abstract] [Full Text] [Related]

  • 17. Long-term disability and prognosis in dentatorubral-pallidoluysian atrophy: a correlation with CAG repeat length.
    Hasegawa A, Ikeuchi T, Koike R, Matsubara N, Tsuchiya M, Nozaki H, Homma A, Idezuka J, Nishizawa M, Onodera O.
    Mov Disord; 2010 Aug 15; 25(11):1694-700. PubMed ID: 20589872
    [Abstract] [Full Text] [Related]

  • 18. [Autosomal dominant spinocerebellar ataxia].
    Legros B, Manto MU.
    Rev Med Brux; 1999 Dec 15; 20(6):495-503. PubMed ID: 10672773
    [Abstract] [Full Text] [Related]

  • 19. Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain.
    Yazawa I, Nukina N, Hashida H, Goto J, Yamada M, Kanazawa I.
    Nat Genet; 1995 May 15; 10(1):99-103. PubMed ID: 7647802
    [Abstract] [Full Text] [Related]

  • 20. Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).
    Koide R, Ikeuchi T, Onodera O, Tanaka H, Igarashi S, Endo K, Takahashi H, Kondo R, Ishikawa A, Hayashi T.
    Nat Genet; 1994 Jan 15; 6(1):9-13. PubMed ID: 8136840
    [Abstract] [Full Text] [Related]

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