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PUBMED FOR HANDHELDS

Journal Abstract Search


368 related items for PubMed ID: 9266429

  • 1. 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
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  • 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
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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. [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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  • 10. GTP cyclohydrolase I activity in mononuclear blood cells in juvenile parkinsonism.
    Ichinose H, Ohye T, Yokochi M, Fujita K, Nagatsu T.
    Neurosci Lett; 1995 May 05; 190(2):140-2. PubMed ID: 7644124
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  • 13. Dopamine transporter density measured by [123I]beta-CIT single-photon emission computed tomography is normal in dopa-responsive dystonia.
    Jeon BS, Jeong JM, Park SS, Kim JM, Chang YS, Song HC, Kim KM, Yoon KY, Lee MC, Lee SB.
    Ann Neurol; 1998 Jun 05; 43(6):792-800. PubMed ID: 9629849
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  • 14. Dopa-responsive dystonia due to a large deletion in the GTP cyclohydrolase I gene.
    Furukawa Y, Guttman M, Sparagana SP, Trugman JM, Hyland K, Wyatt P, Lang AE, Rouleau GA, Shimadzu M, Kish SJ.
    Ann Neurol; 2000 Apr 05; 47(4):517-20. PubMed ID: 10762165
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  • 15. Autosomal dominant GTP cyclohydrolase I (AD GCH 1) deficiency (Segawa disease, dystonia 5; DYT 5).
    Segawa M.
    Chang Gung Med J; 2009 Apr 05; 32(1):1-11. PubMed ID: 19292934
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  • 16. [Hereditary progressive dystonia with marked diurnal fluctuation; dominant Dopa-responsive dystonia linked to GTP cyclohydrolase I gene (HPD/DRD); Segawa's disease].
    Segawa M.
    Ryoikibetsu Shokogun Shirizu; 1999 Apr 05; (27 Pt 2):144-7. PubMed ID: 10434614
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  • 17. [Molecular biology of hereditary dystonia].
    Nagatsu T, Ichinose H.
    No To Hattatsu; 1998 Mar 05; 30(2):93-100. PubMed ID: 9545771
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  • 20. [Dopa-responsive dystonia: clinical, genetic, and biochemical studies].
    Furukawa Y.
    Rinsho Shinkeigaku; 2006 Jan 05; 46(1):19-34. PubMed ID: 16541791
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