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PUBMED FOR HANDHELDS

Journal Abstract Search


223 related items for PubMed ID: 12784278

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  • 8. Functional brain networks in DYT1 dystonia.
    Eidelberg D, Moeller JR, Antonini A, Kazumata K, Nakamura T, Dhawan V, Spetsieris P, deLeon D, Bressman SB, Fahn S.
    Ann Neurol; 1998 Sep; 44(3):303-12. PubMed ID: 9749595
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  • 9. Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystonia.
    Walter M, Bonin M, Pullman RS, Valente EM, Loi M, Gambarin M, Raymond D, Tinazzi M, Kamm C, Glöckle N, Poths S, Gasser T, Bressman SB, Klein C, Ozelius LJ, Riess O, Grundmann K.
    Neurobiol Dis; 2010 May; 38(2):192-200. PubMed ID: 20053375
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  • 12. 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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  • 14. Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystonia.
    Bressman SB, Hunt AL, Heiman GA, Brin MF, Burke RE, Fahn S, Trugman JM, de Leon D, Kramer PL, Wilhelmsen KC.
    Mov Disord; 1994 Nov; 9(6):626-32. PubMed ID: 7845403
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  • 15. Motor deficits and hyperactivity in cerebral cortex-specific Dyt1 conditional knockout mice.
    Yokoi F, Dang MT, Mitsui S, Li J, Li Y.
    J Biochem; 2008 Jan; 143(1):39-47. PubMed ID: 17956903
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  • 16. Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South Tyrol.
    Klein C, Pramstaller PP, Castellan CC, Breakefield XO, Kramer PL, Ozelius LJ.
    Ann Neurol; 1998 Sep; 44(3):394-8. PubMed ID: 9749609
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  • 18. Exclusion of the DYT1 locus in familial torticollis.
    Bressman SB, Warner TT, Almasy L, Uitti RJ, Greene PE, Heiman GA, Raymond D, Ford B, de Leon D, Fahn S, Kramer PL, Risch NJ, Maraganore DM, Nygaard TG, Harding AE.
    Ann Neurol; 1996 Oct; 40(4):681-4. PubMed ID: 8871591
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  • 19. A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia.
    Slominsky PA, Markova ED, Shadrina MI, Illarioshkin SN, Miklina NI, Limborska SA, Ivanova-Smolenskaya IA.
    Hum Mutat; 1999 Sep 19; 14(3):269. PubMed ID: 10477437
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