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Journal Abstract Search

102 related items for PubMed ID: 2324593

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  • 2. Hereditary progressive dystonia with marked diurnal fluctuation. Pathophysiological importance of the age of onset.
    Segawa M, Nomura Y.
    Adv Neurol; 1993; 60():568-76. PubMed ID: 8420193
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  • 4. Hereditary progressive dystonia with marked diurnal fluctuation--consideration on its pathophysiology based on the characteristics of clinical and polysomnographical findings.
    Segawa M, Nomura Y, Tanaka S, Hakamada S, Nagata E, Soda M, Kase M.
    Adv Neurol; 1988; 50():367-76. PubMed ID: 3041759
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  • 9. 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; 40(5):796-8. PubMed ID: 8957022
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  • 11. 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; 37(3):405-8. PubMed ID: 7695242
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  • 17. [Hereditary progressive dystonia with marked diurnal fluctuation--clinical features and GTP cyclohydrolase I gene mutations].
    Tamaru Y, Ito H, Imai T, Hirano M, Ueno S.
    Nihon Rinsho; 1997 Jan; 55(1):135-8. PubMed ID: 9014437
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  • 18. Cases of dopa-responsive dystonia (Segawa disease) in Estonia.
    Talvik I, Segawa M, Veri K, Gross-Paju K, Talvik T.
    Brain Dev; 2010 May; 32(5):428-31. PubMed ID: 19427147
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  • 19. Dopa responsive dystonia in a girl with vitiligo.
    Chaudhary N, Mani J, Rawat S, Mulye R, Shah P.
    Indian Pediatr; 1998 Jul; 35(7):663-5. PubMed ID: 10216678
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  • 20. Dopa-responsive dystonia. Delineation of the clinical syndrome and clues to pathogenesis.
    Nygaard TG.
    Adv Neurol; 1993 Jul; 60():577-85. PubMed ID: 8420194
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