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Journal Abstract Search

131 related items for PubMed ID: 8836972

  • 1. The relationship between trinucleotide repeat length and phenotypic variation in Machado-Joseph disease.
    Matsumura R, Takayanagi T, Fujimoto Y, Murata K, Mano Y, Horikawa H, Chuma T.
    J Neurol Sci; 1996 Jul; 139(1):52-7. PubMed ID: 8836972
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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; 39(4):490-9. PubMed ID: 8619527
    [Abstract] [Full Text] [Related]

  • 4. Muscle excitability abnormalities in Machado-Joseph disease.
    França MC, D'Abreu A, Nucci A, Lopes-Cendes I.
    Arch Neurol; 2008 Apr; 65(4):525-9. PubMed ID: 18413477
    [Abstract] [Full Text] [Related]

  • 5. [Some problems on the clinical phenotype of Machado-Joseph disease in relation between their ages at onset].
    Iwabuchi K, Kogure T, Oda T, Kato Y, Ohtani K, Endo K, Kosaka K, Amano N, Yagishita S.
    No To Shinkei; 1993 Mar; 45(3):246-54. PubMed ID: 8323819
    [Abstract] [Full Text] [Related]

  • 6. 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 Mar; 11(1):23-7. PubMed ID: 9450899
    [Abstract] [Full Text] [Related]

  • 7. 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; 61(2):209-12. PubMed ID: 14967767
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Machado-Joseph disease.
    Sudarsky L, Coutinho P.
    Clin Neurosci; 1995 Mar; 3(1):17-22. PubMed ID: 7614089
    [Abstract] [Full Text] [Related]

  • 10. Analysis of CAG trinucleotide expansion associated with Machado-Joseph disease.
    Watanabe M, Abe K, Aoki M, Kameya T, Kaneko J, Shoji M, Ikeda M, Shizuka M, Ikeda Y, Iizuka T, Hirai S, Itoyama Y.
    J Neurol Sci; 1996 Mar; 136(1-2):101-7. PubMed ID: 8815156
    [Abstract] [Full Text] [Related]

  • 11. Machado-Joseph disease/SCA3 and myotonic dystrophy type 1 in a single patient.
    Miura S, Ohyagi Y, Miike T, Noda K, Motomura K, Ayabe M, Aizawa H, Taniwaki T.
    Clin Neurol Neurosurg; 2009 Dec; 111(10):791-4. PubMed ID: 19713033
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Cognitive impairments in Machado-Joseph disease.
    Kawai Y, Takeda A, Abe Y, Washimi Y, Tanaka F, Sobue G.
    Arch Neurol; 2004 Nov; 61(11):1757-60. PubMed ID: 15534186
    [Abstract] [Full Text] [Related]

  • 14. Machado-Joseph shoe.
    Liu CS, Hsieh M, Chen YY, Lo MC.
    Mov Disord; 2005 Jan; 20(1):66-8. PubMed ID: 15390034
    [Abstract] [Full Text] [Related]

  • 15. Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation.
    Schöls L, Amoiridis G, Epplen JT, Langkafel M, Przuntek H, Riess O.
    J Neurol Neurosurg Psychiatry; 1996 Nov; 61(5):466-70. PubMed ID: 8937340
    [Abstract] [Full Text] [Related]

  • 16. Progression of ataxia in patients with Machado-Joseph disease.
    França MC, D'Abreu A, Nucci A, Cendes F, Lopes-Cendes I.
    Mov Disord; 2009 Jul 15; 24(9):1387-90. PubMed ID: 19441132
    [Abstract] [Full Text] [Related]

  • 17. 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 15; 36(3):258-9. PubMed ID: 10204858
    [Abstract] [Full Text] [Related]

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  • 19. [Molecular genetics of Machado-Joseph disease].
    Kawakami H, Maruyama H, Nakamura S.
    Nihon Rinsho; 1996 Mar 15; 54(3):854-60. PubMed ID: 8904248
    [Abstract] [Full Text] [Related]

  • 20. [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 15; 16(5):281-4. PubMed ID: 10514531
    [Abstract] [Full Text] [Related]

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