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Journal Abstract Search

176 related items for PubMed ID: 8780110

  • 21. High-intensity proton and T2-weighted MRI signals in the globus pallidus in juvenile-type of dentatorubral and pallidoluysian atrophy.
    Imamura A, Ito R, Tanaka S, Fukutomi O, Shimozawa N, Nishimura M, Suzuki Y, Kondo N, Yamada M, Orii T.
    Neuropediatrics; 1994 Oct; 25(5):234-7. PubMed ID: 7885531
    [Abstract] [Full Text] [Related]

  • 22. Progressive atrophy of cerebellum and brainstem as a function of age and the size of the expanded CAG repeats in the MJD1 gene in Machado-Joseph disease.
    Onodera O, Idezuka J, Igarashi S, Takiyama Y, Endo K, Takano H, Oyake M, Tanaka H, Inuzuka T, Hayashi T, Yuasa T, Ito J, Miyatake T, Tsuji S.
    Ann Neurol; 1998 Mar; 43(3):288-96. PubMed ID: 9506544
    [Abstract] [Full Text] [Related]

  • 23. [Molecular genetics of hereditary spinocerebellar ataxia].
    Tsuji S.
    No To Shinkei; 1995 Oct; 47(10):955-61. PubMed ID: 7577140
    [No Abstract] [Full Text] [Related]

  • 24. Clinical and electroencephalographic findings in juvenile type DRPLA.
    Saitoh S, Momoi MY, Yamagata T, Miyao M, Suwa K.
    Pediatr Neurol; 1998 Mar; 18(3):265-8. PubMed ID: 9568927
    [Abstract] [Full Text] [Related]

  • 25. Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: the mutant allele is preferentially transmitted in male meiosis.
    Ikeuchi T, Igarashi S, Takiyama Y, Onodera O, Oyake M, Takano H, Koide R, Tanaka H, Tsuji S.
    Am J Hum Genet; 1996 Apr; 58(4):730-3. PubMed ID: 8644735
    [Abstract] [Full Text] [Related]

  • 26. [Sisters with early onset hereditary dentatorubral-pallidoluysian atrophy of childhood--DNA analysis and clinicopathological findings].
    Yamashita S, Iwamoto H, Hara M, Kondo I, Shimasaki Y, Higashi K, Miyake S, Yamada M.
    No To Hattatsu; 1995 Nov; 27(6):473-9. PubMed ID: 8534513
    [Abstract] [Full Text] [Related]

  • 27. [Genetic analysis including predictive DNA testing in a Japanese family with dentatorubral-pallidoluysian atrophy].
    Nishio H, Wada H, Lee MJ, Matsuo T.
    No To Hattatsu; 1998 Nov; 30(6):512-6. PubMed ID: 9844416
    [Abstract] [Full Text] [Related]

  • 28. Mutation detection in Machado-Joseph disease using repeat expansion detection.
    Lindblad K, Lunkes A, Maciel P, Stevanin G, Zander C, Klockgether T, Ratzlaff T, Brice A, Rouleau GA, Hudson T, Auburger G, Schalling M.
    Mol Med; 1996 Jan; 2(1):77-85. PubMed ID: 8900536
    [Abstract] [Full Text] [Related]

  • 29. Maternal anticipation in Machado-Joseph disease (MJD): some maternal factors independent of the number of CAG repeat units may play a role in genetic anticipation in a Japanese MJD family.
    Takiyama Y, Shimazaki H, Morita M, Soutome M, Sakoe K, Esumi E, Muramatsu S, Yoshida M, Igarashi S, Tanaka H, Tsuji S, Sasaki H, Wakisaka A, Nakano I, Nishizawa M.
    J Neurol Sci; 1998 Mar 05; 155(2):141-5. PubMed ID: 9562258
    [Abstract] [Full Text] [Related]

  • 30. 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 05; 41(4):505-11. PubMed ID: 9124808
    [Abstract] [Full Text] [Related]

  • 31. Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigrees.
    Becher MW, Rubinsztein DC, Leggo J, Wagster MV, Stine OC, Ranen NG, Franz ML, Abbott MH, Sherr M, MacMillan JC, Barron L, Porteous M, Harper PS, Ross CA.
    Mov Disord; 1997 Jul 05; 12(4):519-30. PubMed ID: 9251070
    [Abstract] [Full Text] [Related]

  • 32.
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  • 33. 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 05; 36(3):258-9. PubMed ID: 10204858
    [Abstract] [Full Text] [Related]

  • 34. Machado-Joseph disease: cerebellar ataxia and autonomic dysfunction in a patient with the shortest known expanded allele (56 CAG repeat units) of the MJD1 gene.
    Takiyama Y, Sakoe K, Nakano I, Nishizawa M.
    Neurology; 1997 Aug 05; 49(2):604-6. PubMed ID: 9270607
    [Abstract] [Full Text] [Related]

  • 35. Dentatorubro-pallidoluysian atrophy of the myoclonus epilepsy type with posterior column degeneration.
    Pfeiffer RF, McComb RD.
    Mov Disord; 1990 Aug 05; 5(2):134-8. PubMed ID: 2109190
    [Abstract] [Full Text] [Related]

  • 36. 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]

  • 37. 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 29; 38(1):68-72. PubMed ID: 7611728
    [Abstract] [Full Text] [Related]

  • 38. [Molecular genetics of Machado-Joseph disease].
    Kawakami H, Maruyama H, Nakamura S.
    Nihon Rinsho; 1996 Mar 29; 54(3):854-60. PubMed ID: 8904248
    [Abstract] [Full Text] [Related]

  • 39. 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]

  • 40.
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