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Journal Abstract Search

152 related items for PubMed ID: 11584049

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  • 7. De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia.
    Klein C, Brin MF, de Leon D, Limborska SA, Ivanova-Smolenskaya IA, Bressman SB, Friedman A, Markova ED, Risch NJ, Breakefield XO, Ozelius LJ.
    Hum Mol Genet; 1998 Jul; 7(7):1133-6. PubMed ID: 9618171
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  • 8. Inherited and de novo mutations in sporadic cases of DYT1-dystonia.
    Hjermind LE, Werdelin LM, Sørensen SA.
    Eur J Hum Genet; 2002 Mar; 10(3):213-6. PubMed ID: 11973627
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  • 9. [Early-onset torsion dystonia linked to chromosome 9q34: DYT1].
    Nomura Y.
    Ryoikibetsu Shokogun Shirizu; 1999 Mar; (27 Pt 2):139-43. PubMed ID: 10434613
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  • 12. DYT1 mutations in early onset primary torsion dystonia and Parkinson disease patients in Chinese populations.
    Yang JF, Wu T, Li JY, Li YJ, Zhang YL, Chan P.
    Neurosci Lett; 2009 Jan 30; 450(2):117-21. PubMed ID: 19038309
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  • 13. To test or not to test? That is the question (with a twist).
    Lichter DG, Lang AE.
    Neurology; 2000 May 09; 54(9):1718-9. PubMed ID: 10802773
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  • 14. Clinical and genetic evaluation of DYT1 and DYT6 primary dystonia in China.
    Cheng FB, Wan XH, Feng JC, Wang L, Yang YM, Cui LY.
    Eur J Neurol; 2011 Mar 09; 18(3):497-503. PubMed ID: 20825472
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  • 15. Frequency of the DYT1 mutation in primary torsion dystonia without family history.
    Brassat D, Camuzat A, Vidailhet M, Feki I, Jedynak P, Klap P, Agid Y, Dürr A, Brice A.
    Arch Neurol; 2000 Mar 09; 57(3):333-5. PubMed ID: 10714658
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  • 16. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.
    Ozelius LJ, Hewett JW, Page CE, Bressman SB, Kramer PL, Shalish C, de Leon D, Brin MF, Raymond D, Corey DP, Fahn S, Risch NJ, Buckler AJ, Gusella JF, Breakefield XO.
    Nat Genet; 1997 Sep 09; 17(1):40-8. PubMed ID: 9288096
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  • 17. [Molecular-genetic analysis of torsion dystonia in Russia].
    Markova ED, Slominskiĭ PA, Illarioshkin SN, Miklina NI, Shadrina MI, Popova SN, Limborskaia SA, Ivanova-Smolenskaia IA.
    Genetika; 2000 Jul 09; 36(7):952-8. PubMed ID: 10994500
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  • 18. The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews.
    Kramer PL, Heiman GA, Gasser T, Ozelius LJ, de Leon D, Brin MF, Burke RE, Hewett J, Hunt AL, Moskowitz C.
    Am J Hum Genet; 1994 Sep 09; 55(3):468-75. PubMed ID: 8079990
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  • 19. DYT1 mutation in Japanese patients with primary torsion dystonia.
    Matsumoto S, Nishimura M, Kaji R, Sakamoto T, Mezaki T, Shimazu H, Murase N, Shibasaki H.
    Neuroreport; 2001 Mar 26; 12(4):793-5. PubMed ID: 11277585
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  • 20. A study of idiopathic torsion dystonia in a non-Jewish family: evidence for genetic heterogeneity.
    Bressman SB, Heiman GA, Nygaard TG, Ozelius LJ, Hunt AL, Brin MF, Gordon MF, Moskowitz CB, de Leon D, Burke RE.
    Neurology; 1994 Feb 26; 44(2):283-7. PubMed ID: 8309575
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