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216 related items for PubMed ID: 9545771
1. [Molecular biology of hereditary dystonia]. Nagatsu T, Ichinose H. No To Hattatsu; 1998 Mar; 30(2):93-100. PubMed ID: 9545771 [Abstract] [Full Text] [Related]
2. Molecular genetics of hereditary dystonia--mutations in the GTP cyclohydrolase I gene. Ichinose H, Nagatsu T. Brain Res Bull; 1997 Mar; 43(1):35-8. PubMed ID: 9205791 [Abstract] [Full Text] [Related]
11. 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 [Abstract] [Full Text] [Related]
12. 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; 50(4):1015-20. PubMed ID: 9566388 [Abstract] [Full Text] [Related]
17. Characterization of mouse and human GTP cyclohydrolase I genes. Mutations in patients with GTP cyclohydrolase I deficiency. Ichinose H, Ohye T, Matsuda Y, Hori T, Blau N, Burlina A, Rouse B, Matalon R, Fujita K, Nagatsu T. J Biol Chem; 1995 Apr 28; 270(17):10062-71. PubMed ID: 7730309 [Abstract] [Full Text] [Related]
19. 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 28; 43(6):792-800. PubMed ID: 9629849 [Abstract] [Full Text] [Related]
20. Characterization of wild-type and mutants of recombinant human GTP cyclohydrolase I: relationship to etiology of dopa-responsive dystonia. Suzuki T, Ohye T, Inagaki H, Nagatsu T, Ichinose H. J Neurochem; 1999 Dec 28; 73(6):2510-6. PubMed ID: 10582612 [Abstract] [Full Text] [Related] Page: [Next] [New Search]