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Journal Abstract Search

158 related items for PubMed ID: 15293281

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  • 6. Different patterns of electrophysiological deficits in manifesting and non-manifesting carriers of the DYT1 gene mutation.
    Edwards MJ, Huang YZ, Wood NW, Rothwell JC, Bhatia KP.
    Brain; 2003 Sep; 126(Pt 9):2074-80. PubMed ID: 12821514
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  • 7. Subcellular distribution of THAP1 and alterations in the microstructure of brain white matter in DYT6 dystonia.
    Cheng FB, Wan XH, Feng JC, Ma LY, Hou B, Feng F, Wang L, Yang YM.
    Parkinsonism Relat Disord; 2012 Sep; 18(8):978-82. PubMed ID: 22652465
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  • 10. Increased sensorimotor network activity in DYT1 dystonia: a functional imaging study.
    Carbon M, Argyelan M, Habeck C, Ghilardi MF, Fitzpatrick T, Dhawan V, Pourfar M, Bressman SB, Eidelberg D.
    Brain; 2010 Mar; 133(Pt 3):690-700. PubMed ID: 20207699
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  • 11. Genetics of dystonia: an overview.
    Bressman SB.
    Parkinsonism Relat Disord; 2007 Mar; 13 Suppl 3():S347-55. PubMed ID: 18267263
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  • 13. Gray and white matter changes in Alzheimer's disease: a diffusion tensor imaging study.
    Rose SE, Janke AL, Chalk JB.
    J Magn Reson Imaging; 2008 Jan; 27(1):20-6. PubMed ID: 18050329
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  • 15. DYT1 mutation in Korean primary dystonia patients.
    Im JH, Ahn TB, Kim KB, Ko SB, Jeon BS.
    Parkinsonism Relat Disord; 2004 Oct; 10(7):421-3. PubMed ID: 15465399
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  • 16. Impaired sequence learning in dystonia mutation carriers: a genotypic effect.
    Carbon M, Argyelan M, Ghilardi MF, Mattis P, Dhawan V, Bressman S, Eidelberg D.
    Brain; 2011 May; 134(Pt 5):1416-27. PubMed ID: 21515903
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  • 19. Neuropsychological profile of DYT1 dystonia.
    Balas M, Peretz C, Badarny S, Scott RB, Giladi N.
    Mov Disord; 2006 Dec; 21(12):2073-7. PubMed ID: 17013905
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