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Journal Abstract Search
368 related items for PubMed ID: 9266429
1. GTP cyclohydrolase I gene, dystonia, juvenile parkinsonism, and Parkinson's disease. Nagatsu T, Ichinose H. J Neural Transm Suppl; 1997; 49():203-9. PubMed ID: 9266429 [Abstract] [Full Text] [Related]
5. GTP-cyclohydrolase I gene mutations in hereditary progressive amd dopa-responsive dystonia. Furukawa Y, Shimadzu M, Rajput AH, Shimizu Y, Tagawa T, Mori H, Yokochi M, Narabayashi H, Hornykiewicz O, Mizuno Y, Kish SJ. Ann Neurol; 1996 May; 39(5):609-17. PubMed ID: 8619546 [Abstract] [Full Text] [Related]
6. [The relation between metabolism of biopterin and dystonia-parkinsonism]. Ichinose H, Ohye T, Suzuki T, Inagaki H, Nagatsu T. Nihon Shinkei Seishin Yakurigaku Zasshi; 1999 Apr; 19(2):85-9. PubMed ID: 10464780 [Abstract] [Full Text] [Related]
13. 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 05; 43(6):792-800. PubMed ID: 9629849 [Abstract] [Full Text] [Related]
14. Dopa-responsive dystonia due to a large deletion in the GTP cyclohydrolase I gene. Furukawa Y, Guttman M, Sparagana SP, Trugman JM, Hyland K, Wyatt P, Lang AE, Rouleau GA, Shimadzu M, Kish SJ. Ann Neurol; 2000 Apr 05; 47(4):517-20. PubMed ID: 10762165 [Abstract] [Full Text] [Related]
15. Autosomal dominant GTP cyclohydrolase I (AD GCH 1) deficiency (Segawa disease, dystonia 5; DYT 5). Segawa M. Chang Gung Med J; 2009 Apr 05; 32(1):1-11. PubMed ID: 19292934 [Abstract] [Full Text] [Related]
16. [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 Apr 05; (27 Pt 2):144-7. PubMed ID: 10434614 [No Abstract] [Full Text] [Related]
17. [Molecular biology of hereditary dystonia]. Nagatsu T, Ichinose H. No To Hattatsu; 1998 Mar 05; 30(2):93-100. PubMed ID: 9545771 [Abstract] [Full Text] [Related]