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PUBMED FOR HANDHELDS

Journal Abstract Search


219 related items for PubMed ID: 10464780

  • 1. [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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  • 3. [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
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  • 4. [Dopa-responsive dystonia: clinical, genetic, and biochemical studies].
    Furukawa Y.
    Rinsho Shinkeigaku; 2006 Jan; 46(1):19-34. PubMed ID: 16541791
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  • 5. 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
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  • 6. [Molecular genetics of hereditary progressive dystonia (HPD/Segawa's disease)].
    Ichinose H, Nagatsu T.
    Nihon Rinsho; 1996 May; 54(5):1453-9. PubMed ID: 8965384
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  • 9. 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
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  • 10. Dystonia with motor delay in compound heterozygotes for GTP-cyclohydrolase I gene mutations.
    Furukawa Y, Kish SJ, Bebin EM, Jacobson RD, Fryburg JS, Wilson WG, Shimadzu M, Hyland K, Trugman JM.
    Ann Neurol; 1998 Jul; 44(1):10-6. PubMed ID: 9667588
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  • 12. Tetrahydrobiopterin metabolism and GTP cyclohydrolase I mutations in L-dopa-responsive dystonia.
    Bezin L, Anastasiadis PZ, Nygaard TG, Levine RA.
    Adv Neurol; 1998 Jul; 78():291-300. PubMed ID: 9750925
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  • 13. GTP cyclohydrolase regulation: implications for brain development and function.
    Ichinose H, Homma D, Sumi-Ichinose C, Nomura T, Kondo K.
    Adv Pharmacol; 2013 Jul; 68():23-35. PubMed ID: 24054139
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  • 19. Is phenotypic variation of hereditary progressive dystonia with marked diurnal fluctuation/dopa-responsive dystonia (HPD/DRD) caused by the difference of the locus of mutation on the GTP cyclohydrolase 1 (GCH-1) gene?
    Segawa M, Nomura Y, Yukishita S, Nishiyama N, Yokochi M.
    Adv Neurol; 2004 Jul; 94():217-23. PubMed ID: 14509676
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  • 20. [Segawa disease].
    Nomura Y.
    Rinsho Shinkeigaku; 1997 Dec; 37(12):1137-8. PubMed ID: 9577670
    [Abstract] [Full Text] [Related]


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