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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

287 related items for PubMed ID: 12134322

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  • 2. DOPA-sensitive progressive dystonia of childhood with fluctuations of symptoms--Segawa's syndrome and possible variants. Results of a collaborative study of the European Federation of Child Neurology Societies (EFCNS).
    Deonna T.
    Neuropediatrics; 1986 May; 17(2):81-5. PubMed ID: 3724992
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  • 4. Anaesthesia for caesarean section in a patient with dopa-responsive dystonia or Segawa's syndrome.
    Sinha A, Hartsilver EL.
    Int J Obstet Anesth; 2009 Jan; 18(1):67-72. PubMed ID: 19022657
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  • 6. [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 Jan; (27 Pt 2):144-7. PubMed ID: 10434614
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  • 7. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene.
    Ichinose H, Ohye T, Takahashi E, Seki N, Hori T, Segawa M, Nomura Y, Endo K, Tanaka H, Tsuji S.
    Nat Genet; 1994 Nov; 8(3):236-42. PubMed ID: 7874165
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  • 10. The perinatal emphasis of Segawa's syndrome.
    Lurie S, Priscu V, Hagay Z.
    J Perinat Med; 1996 Nov; 24(6):699-701. PubMed ID: 9120755
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  • 14. Familial dopa-responsive cervical dystonia.
    Schneider SA, Mohire MD, Trender-Gerhard I, Asmus F, Sweeney M, Davis M, Gasser T, Wood NW, Bhatia KP.
    Neurology; 2006 Feb 28; 66(4):599-601. PubMed ID: 16505323
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  • 18. The gene for hereditary progressive dystonia with marked diurnal fluctuation maps to chromosome 14q.
    Tanaka H, Endo K, Tsuji S, Nygaard TG, Weeks DE, Nomura Y, Segawa M.
    Ann Neurol; 1995 Mar 28; 37(3):405-8. PubMed ID: 7695242
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  • 20. Mutant GTP cyclohydrolase I mRNA levels contribute to dopa-responsive dystonia onset.
    Hirano M, Tamaru Y, Ito H, Matsumoto S, Imai T, Ueno S.
    Ann Neurol; 1996 Nov 28; 40(5):796-8. PubMed ID: 8957022
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