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10. 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 [TBL] [Abstract][Full Text] [Related]
11. 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; 94():217-23. PubMed ID: 14509676 [No Abstract] [Full Text] [Related]
12. Autosomal dominant GTP cyclohydrolase I (AD GCH 1) deficiency (Segawa disease, dystonia 5; DYT 5). Segawa M Chang Gung Med J; 2009; 32(1):1-11. PubMed ID: 19292934 [TBL] [Abstract][Full Text] [Related]
13. Intracortical inhibition of the motor cortex in Segawa disease (DYT5). Hanajima R; Nomura Y; Segawa M; Ugawa Y Neurology; 2007 Mar; 68(13):1039-44. PubMed ID: 17389309 [TBL] [Abstract][Full Text] [Related]