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Journal Abstract Search

520 related items for PubMed ID: 19065526

  • 1.
    ; . PubMed ID:
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  • 2. Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic.
    Wang YG, Du J, Wang JL, Chen J, Chen C, Luo YY, Xiao ZQ, Jiang H, Yan XX, Xia K, Pan Q, Tang BS, Shen L.
    J Neurol Sci; 2009 Oct 15; 285(1-2):121-4. PubMed ID: 19608203
    [Abstract] [Full Text] [Related]

  • 3. Machado-Joseph disease/spinocerebellar ataxia type 3.
    Paulson H.
    Handb Clin Neurol; 2012 Oct 15; 103():437-49. PubMed ID: 21827905
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  • 5. Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): a two-case report.
    Bettencourt C, Santos C, Coutinho P, Rizzu P, Vasconcelos J, Kay T, Cymbron T, Raposo M, Heutink P, Lima M.
    BMC Neurol; 2011 Oct 24; 11():131. PubMed ID: 22023810
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  • 7. Ataxin-3 protein modification as a treatment strategy for spinocerebellar ataxia type 3: removal of the CAG containing exon.
    Evers MM, Tran HD, Zalachoras I, Pepers BA, Meijer OC, den Dunnen JT, van Ommen GJ, Aartsma-Rus A, van Roon-Mom WM.
    Neurobiol Dis; 2013 Oct 24; 58():49-56. PubMed ID: 23659897
    [Abstract] [Full Text] [Related]

  • 8. Polyglutamine diseases: the special case of ataxin-3 and Machado-Joseph disease.
    Matos CA, de Macedo-Ribeiro S, Carvalho AL.
    Prog Neurobiol; 2011 Sep 15; 95(1):26-48. PubMed ID: 21740957
    [Abstract] [Full Text] [Related]

  • 9. [Clinical features and gene mutation analysis in Machado-Joseph disease of spinocerebellar ataxia type 3 in littoral of Zhejiang].
    Jin YY, Zeng AP, Cai HB, Wu F, Feng Z, Hong Q, Zhang L, Jiang ZK.
    Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi; 2009 Apr 15; 23(2):132-4. PubMed ID: 20104758
    [Abstract] [Full Text] [Related]

  • 10. A mutant ataxin-3 fragment results from processing at a site N-terminal to amino acid 190 in brain of Machado-Joseph disease-like transgenic mice.
    Colomer Gould VF, Goti D, Pearce D, Gonzalez GA, Gao H, Bermudez de Leon M, Jenkins NA, Copeland NG, Ross CA, Brown DR.
    Neurobiol Dis; 2007 Sep 15; 27(3):362-9. PubMed ID: 17632007
    [Abstract] [Full Text] [Related]

  • 11. [Polyglutamine-expanded ataxin-3 is degraded by autophagy].
    Xiao H, Tang J, Hu Z, Tan J, Tang B, Jiang Z.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Feb 15; 27(1):23-8. PubMed ID: 20140862
    [Abstract] [Full Text] [Related]

  • 12. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia.
    Geschwind DH, Perlman S, Figueroa CP, Treiman LJ, Pulst SM.
    Am J Hum Genet; 1997 Apr 15; 60(4):842-50. PubMed ID: 9106530
    [Abstract] [Full Text] [Related]

  • 13. 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 Apr 15; 11(1):23-7. PubMed ID: 9450899
    [Abstract] [Full Text] [Related]

  • 14. Machado-Joseph disease and other rare spinocerebellar ataxias.
    Matilla-Dueñas A.
    Adv Exp Med Biol; 2012 Apr 15; 724():172-88. PubMed ID: 22411243
    [Abstract] [Full Text] [Related]

  • 15. Mutational origin of Machado-Joseph disease in the Australian Aboriginal communities of Groote Eylandt and Yirrkala.
    Martins S, Soong BW, Wong VC, Giunti P, Stevanin G, Ranum LP, Sasaki H, Riess O, Tsuji S, Coutinho P, Amorim A, Sequeiros J, Nicholson GA.
    Arch Neurol; 2012 Jun 15; 69(6):746-51. PubMed ID: 22351852
    [Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of Machado-Joseph disease/Spinocerebellar Ataxia Type 3 in Taiwan: early detection of expanded ataxin-3.
    Tsai HF, Liu CS, Chen GD, Lin ML, Li C, Chen YY, Wang BT, Hsieh M.
    J Clin Lab Anal; 2003 Jun 15; 17(5):195-200. PubMed ID: 12938149
    [Abstract] [Full Text] [Related]

  • 17. Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients.
    Schöls L, Vieira-Saecker AM, Schöls S, Przuntek H, Epplen JT, Riess O.
    Hum Mol Genet; 1995 Jun 15; 4(6):1001-5. PubMed ID: 7655453
    [Abstract] [Full Text] [Related]

  • 18. The role of the mammalian DNA end-processing enzyme polynucleotide kinase 3'-phosphatase in spinocerebellar ataxia type 3 pathogenesis.
    Chatterjee A, Saha S, Chakraborty A, Silva-Fernandes A, Mandal SM, Neves-Carvalho A, Liu Y, Pandita RK, Hegde ML, Hegde PM, Boldogh I, Ashizawa T, Koeppen AH, Pandita TK, Maciel P, Sarkar PS, Hazra TK.
    PLoS Genet; 2015 Jan 15; 11(1):e1004749. PubMed ID: 25633985
    [Abstract] [Full Text] [Related]

  • 19. Caring for Machado-Joseph disease: current understanding and how to help patients.
    D'Abreu A, França MC, Paulson HL, Lopes-Cendes I.
    Parkinsonism Relat Disord; 2010 Jan 15; 16(1):2-7. PubMed ID: 19811945
    [Abstract] [Full Text] [Related]

  • 20. Characterization of the rat spinocerebellar ataxia type 3 gene.
    Schmitt I, Brattig T, Gossen M, Riess O.
    Neurogenetics; 1997 Sep 15; 1(2):103-12. PubMed ID: 10732811
    [Abstract] [Full Text] [Related]

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