総説・解説記事- 北本 哲之 -
表示方法: 表示形式: 表示順:
件数:12件
[2004]
1.[Iatrogenic Creutzfeldt-Jakob disease] (Nippon Rinsho).[Nippon Rinsho,62 Suppl, (2004), 248-251]Satoh Katsuya, Shirabe Susumu, Katamine Shigeru, Muramoto Tamaki, Kitamoto Tetsuyuki
[2001]
2.[Prion diseases, update] (Rinsho Shinkeigaku).[Rinsho Shinkeigaku,41(12), (2001), 1223-1225]Kitamoto T
[2000]
3.[Prion diseases] (Nippon Ronen Igakkai Zasshi).[Nippon Ronen Igakkai Zasshi,37(10), (2000), 780-781]Kitamoto T
4.Creutzfeldt-Jakob disease. (Neuropathology).[Neuropathology,20 Suppl, (2000), S52-4]Kitamoto T
5.Analyses of Gerstmann-Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219Glu. (Neurosci Lett).[Neurosci Lett,288(3), (2000), 179-182]Muramoto T, Tanaka T, Kitamoto N, Sano C, Hayashi Y, Kutomi T, Yutani C, Kitamoto T
[1996]
6.Human prion disease and human prion protein disease. (Curr Top Microbiol Immunol).[Curr Top Microbiol Immunol,207, (1996), 27-34]Kitamoto T, Tateishi J
7.[Prion diseases in dementia] (Nippon Ronen Igakkai Zasshi).[Nippon Ronen Igakkai Zasshi,33(3), (1996), 178-179]Kitamoto T
[1995]
8.Inherited prion diseases and transmission to rodents. (Brain Pathol).[Brain Pathol,5(1), (1995), 53-59]Tateishi J, Kitamoto T
[1994]
9.[Molecular genetics in Creutzfeldt-Jakob disease] (Rinsho Shinkeigaku).[Rinsho Shinkeigaku,34(12), (1994), 1222-1223]Kitamoto T
10.Human prion diseases with variant prion protein. (Philos Trans R Soc Lond B Biol Sci).[Philos Trans R Soc Lond B Biol Sci,343(1306), (1994), 391-398]Kitamoto T, Tateishi J
[1993]
11.Developments in diagnosis for prion diseases. (Br Med Bull).[Br Med Bull,49(4), (1993), 971-979]Tateishi J, Kitamoto T
[1991]
12.Modified tau is present in younger nondemented persons: a study of subcortical nuclei in Alzheimer's disease and progressive supranuclear palsy. (Acta Neuropathol).[Acta Neuropathol,81(5), (1991), 517-523]Shin R W, Kitamoto T, Tateishi J
Page: [1]
戻るこのページのトップへ
copyright(c)2005 Tohoku University