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Journal Abstract Search

203 related items for PubMed ID: 18044725

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  • 9. Clinical similarities of hereditary progressive/dopa responsive dystonia caused by different types of mutations in the GTP cyclohydrolase I gene.
    Tamaru Y, Hirano M, Ito H, Kawamura J, Matsumoto S, Imai T, Ueno S.
    J Neurol Neurosurg Psychiatry; 1998 Apr; 64(4):469-73. PubMed ID: 9576537
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  • 10. GCH1 mutation and clinical study of Chinese patients with dopa-responsive dystonia.
    Liu X, Zhang SS, Fang DF, Ma MY, Guo XY, Yang Y, Shang HF.
    Mov Disord; 2010 Mar 15; 25(4):447-51. PubMed ID: 20108370
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    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Furukawa Y.
    ; 1993 Mar 15. PubMed ID: 20301681
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  • 12. Mutations of GCH1 in Dopa-responsive dystonia.
    Müller U, Steinberger D, Topka H.
    J Neural Transm (Vienna); 2002 Mar 15; 109(3):321-8. PubMed ID: 11956954
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  • 16. A new mutation of GCH1 in triplets family with dopa-responsive dystonia.
    Tachi N, Takahashi S, Jo M, Shinoda M.
    Eur J Neurol; 2011 Sep 15; 18(9):1191-3. PubMed ID: 21834904
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  • 19. Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystonia.
    Furukawa Y, Lang AE, Trugman JM, Bird TD, Hunter A, Sadeh M, Tagawa T, St George-Hyslop PH, Guttman M, Morris LW, Hornykiewicz O, Shimadzu M, Kish SJ.
    Neurology; 1998 Apr 15; 50(4):1015-20. PubMed ID: 9566388
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  • 20. Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity.
    Bandmann O, Nygaard TG, Surtees R, Marsden CD, Wood NW, Harding AE.
    Hum Mol Genet; 1996 Mar 15; 5(3):403-6. PubMed ID: 8852666
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