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Journal Abstract Search

320 related items for PubMed ID: 9703621

  • 1. [Autosomal-dominant DOPA-responsive dystonia, caused by mutations in the GTP-cyclohydrolase I gene].
    Nagatsu T, Ichinose H.
    Vopr Med Khim; 1998; 44(3):225-8. PubMed ID: 9703621
    [Abstract] [Full Text] [Related]

  • 2. GTP cyclohydrolase I gene, dystonia, juvenile parkinsonism, and Parkinson's disease.
    Nagatsu T, Ichinose H.
    J Neural Transm Suppl; 1997; 49():203-9. PubMed ID: 9266429
    [Abstract] [Full Text] [Related]

  • 3. Molecular genetics of dopa-responsive dystonia.
    Ichinose H, Suzuki T, Inagaki H, Ohye T, Nagatsu T.
    Biol Chem; 1999 Dec; 380(12):1355-64. PubMed ID: 10661862
    [Abstract] [Full Text] [Related]

  • 4. Autosomal dominant GTP cyclohydrolase I (AD GCH 1) deficiency (Segawa disease, dystonia 5; DYT 5).
    Segawa M.
    Chang Gung Med J; 2009 Dec; 32(1):1-11. PubMed ID: 19292934
    [Abstract] [Full Text] [Related]

  • 5. Dopa-responsive dystonia is induced by a dominant-negative mechanism.
    Hwu WL, Chiou YW, Lai SY, Lee YM.
    Ann Neurol; 2000 Oct; 48(4):609-13. PubMed ID: 11026444
    [Abstract] [Full Text] [Related]

  • 6. GTP-cyclohydrolase I gene mutations in hereditary progressive amd dopa-responsive dystonia.
    Furukawa Y, Shimadzu M, Rajput AH, Shimizu Y, Tagawa T, Mori H, Yokochi M, Narabayashi H, Hornykiewicz O, Mizuno Y, Kish SJ.
    Ann Neurol; 1996 May; 39(5):609-17. PubMed ID: 8619546
    [Abstract] [Full Text] [Related]

  • 7. Autosomal dominant guanosine triphosphate cyclohydrolase I deficiency (Segawa disease).
    Segawa M, Nomura Y, Nishiyama N.
    Ann Neurol; 2003 May; 54 Suppl 6():S32-45. PubMed ID: 12891652
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  • 13. [Molecular biology of hereditary dystonia].
    Nagatsu T, Ichinose H.
    No To Hattatsu; 1998 Mar; 30(2):93-100. PubMed ID: 9545771
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  • 14. [The relation between metabolism of biopterin and dystonia-parkinsonism].
    Ichinose H, Ohye T, Suzuki T, Inagaki H, Nagatsu T.
    Nihon Shinkei Seishin Yakurigaku Zasshi; 1999 Apr; 19(2):85-9. PubMed ID: 10464780
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  • 15. [Dopa-responsive dystonia].
    Furukawa Y.
    Rinsho Shinkeigaku; 2006 Nov; 46(11):769-73. PubMed ID: 17432176
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  • 17. Genetics and biochemistry of dopa-responsive dystonia: significance of striatal tyrosine hydroxylase protein loss.
    Furukawa Y.
    Adv Neurol; 2003 Nov; 91():401-10. PubMed ID: 12442699
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  • 18. Tetrahydrobiopterin metabolism and GTP cyclohydrolase I mutations in L-dopa-responsive dystonia.
    Bezin L, Anastasiadis PZ, Nygaard TG, Levine RA.
    Adv Neurol; 1998 Nov; 78():291-300. PubMed ID: 9750925
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  • 19. [Segawa disease (hereditary progressive dystonia with marked diurnal fluctuation-HPD) and abnormalities in pteridin metabolism].
    Segawa M.
    Rinsho Shinkeigaku; 1996 Dec; 36(12):1322-3. PubMed ID: 9128393
    [Abstract] [Full Text] [Related]

  • 20. Segawa's disease: dopa-responsive dystonia.
    Gordon N.
    Int J Clin Pract; 2008 Jun; 62(6):943-6. PubMed ID: 17971156
    [Abstract] [Full Text] [Related]

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