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Journal Abstract Search

176 related items for PubMed ID: 8780110

  • 1. A family with Machado-Joseph disease, previously diagnosed as dentatorubral-pallidoluysian atrophy.
    Sakai T, Antoku Y, Kawakami H, Maruyama H, Nakamura S, Tanaka K.
    Neurology; 1996 Apr; 46(4):1154-6. PubMed ID: 8780110
    [Abstract] [Full Text] [Related]

  • 2. [Machado-Joseph disease].
    Yuasa T.
    No To Shinkei; 1995 Oct; 47(10):939-45. PubMed ID: 7577138
    [No Abstract] [Full Text] [Related]

  • 3. Somatic mosaicism of the expanded CAG trinucleotide repeat in mRNAs for the responsible gene of Machado-Joseph disease (MJD), dentatorubral-pallidoluysian atrophy (DRPLA), and spinal and bulbar muscular atrophy (SBMA).
    Ito Y, Tanaka F, Yamamoto M, Doyu M, Nagamatsu M, Riku S, Mitsuma T, Sobue G.
    Neurochem Res; 1998 Jan; 23(1):25-32. PubMed ID: 9482263
    [Abstract] [Full Text] [Related]

  • 4. Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients.
    Silveira I, Lopes-Cendes I, Kish S, Maciel P, Gaspar C, Coutinho P, Botez MI, Teive H, Arruda W, Steiner CE, Pinto-Júnior W, Maciel JA, Jerin S, Sack G, Andermann E, Sudarsky L, Rosenberg R, MacLeod P, Chitayat D, Babul R, Sequeiros J, Rouleau GA.
    Neurology; 1996 Jan; 46(1):214-8. PubMed ID: 8559378
    [Abstract] [Full Text] [Related]

  • 5. Does homozygosity advance the onset of dentatorubral-pallidoluysian atrophy?
    Sato K, Kashihara K, Okada S, Ikeuchi T, Tsuji S, Shomori T, Morimoto K, Hayabara T.
    Neurology; 1995 Oct; 45(10):1934-6. PubMed ID: 7477999
    [Abstract] [Full Text] [Related]

  • 6. [Dentatorubral-pallidoluysian atrophy (DRPLA: differential diagnosis of chorea)].
    Tsuji S.
    Ryoikibetsu Shokogun Shirizu; 1999 Oct; (27 Pt 2):101-3. PubMed ID: 10434603
    [No Abstract] [Full Text] [Related]

  • 7. [Dentatorubral-pallidoluysian atrophy (DRPLA: Naito-Oyanagi disease)].
    Tsuji S.
    Ryoikibetsu Shokogun Shirizu; 1999 Oct; (27 Pt 2):275-9. PubMed ID: 10434650
    [No Abstract] [Full Text] [Related]

  • 8. Dentatorubral-pallidoluysian atrophy (DRPLA): clinical features and molecular genetics.
    Tsuji S.
    Adv Neurol; 1999 Oct; 79():399-409. PubMed ID: 10514829
    [No Abstract] [Full Text] [Related]

  • 9. 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; 135(1):43-50. PubMed ID: 8926495
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  • 13. Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotide repeat expansion in families with autosomal dominant motor disorders, including the Drew family of Walworth.
    Giunti P, Sweeney MG, Harding AE.
    Brain; 1995 Oct; 118 ( Pt 5)():1077-85. PubMed ID: 7496771
    [Abstract] [Full Text] [Related]

  • 14. Genetic analysis of a dentatorubral-pallidoluysian atrophy family: relevance to apparent sporadic cases.
    Hattori M, Yuasa H, Takada K, Yamada T, Yamada K, Kamimoto K, Uchida M.
    Intern Med; 1999 Mar; 38(3):287-9. PubMed ID: 10337944
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  • 15. Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease.
    Higgins JJ, Nee LE, Vasconcelos O, Ide SE, Lavedan C, Goldfarb LG, Polymeropoulos MH.
    Neurology; 1996 Jan; 46(1):208-13. PubMed ID: 8559377
    [Abstract] [Full Text] [Related]

  • 16. [A case of juvenile type dentatorubral-pallidoluysian atrophy (DRPLA) with psychomotor retardation since infancy].
    Wada Y, Matsuoka T, Imai K, Taniike M, Mano T, Ono J, Okada S, Kondo I.
    No To Hattatsu; 1998 Nov; 30(6):543-8. PubMed ID: 9844421
    [Abstract] [Full Text] [Related]

  • 17. [Genes for human brain diseases--dentatorubral-pallidoluysian atrophy].
    Naito H, Tsuji S.
    Tanpakushitsu Kakusan Koso; 1995 Apr; 40(6):829-33. PubMed ID: 7754068
    [No Abstract] [Full Text] [Related]

  • 18. 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 Apr; 3(1):23-7. PubMed ID: 7614090
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  • 20. Single sperm analysis of the CAG repeats in the gene for dentatorubral-pallidoluysian atrophy (DRPLA): the instability of the CAG repeats in the DRPLA gene is prominent among the CAG repeat diseases.
    Takiyama Y, Sakoe K, Amaike M, Soutome M, Ogawa T, Nakano I, Nishizawa M.
    Hum Mol Genet; 1999 Mar; 8(3):453-7. PubMed ID: 9949204
    [Abstract] [Full Text] [Related]

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