315 related articles for article (PubMed ID: 2468821)
1. Positive transmission of Creutzfeldt-Jakob disease verified by murine kuru plaques.
Kitamoto T; Tateishi J; Sawa H; Doh-Ura K
Lab Invest; 1989 Apr; 60(4):507-12. PubMed ID: 2468821
[TBL] [Abstract][Full Text] [Related]
2. Immunohistochemical verification of senile and kuru plaques in Creutzfeldt-Jakob disease and the allied disease.
Kitamoto T; Tateishi J; Sato Y
Ann Neurol; 1988 Oct; 24(4):537-42. PubMed ID: 3071243
[TBL] [Abstract][Full Text] [Related]
3. Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann-Sträussler syndrome.
Doh-ura K; Tateishi J; Kitamoto T; Sasaki H; Sakaki Y
Ann Neurol; 1990 Feb; 27(2):121-6. PubMed ID: 2180366
[TBL] [Abstract][Full Text] [Related]
4. Creutzfeldt-Jakob disease (CJD) of a short duration with prion protein (PrP) plaques.
Liberski PP; Kwieciński H; Barcikowska M; Mirecka B; Kulczycki J; Kida E; Brown P; Gajdusek DC
Patol Pol; 1991; 42(4):115-8. PubMed ID: 1845486
[TBL] [Abstract][Full Text] [Related]
5. [Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Part II].
Zaborowski A
Psychiatr Pol; 2004; 38(2):297-309. PubMed ID: 15307294
[TBL] [Abstract][Full Text] [Related]
6. [Recent advances in the research of Creutzfeldt-Jakob disease (CJD) and Gerstmann-Strüssler syndrome (GSS)].
Tateishi J
Rinsho Shinkeigaku; 1991 Dec; 31(12):1306-8. PubMed ID: 1687809
[TBL] [Abstract][Full Text] [Related]
7. Neuropathology of human prion diseases (spongiform encephalopathies).
Kretzschmar HA
Dev Biol Stand; 1993; 80():71-90. PubMed ID: 8270118
[TBL] [Abstract][Full Text] [Related]
8. Immunohistochemical localization of 14.3.3 zeta protein in amyloid plaques in human spongiform encephalopathies.
Richard M; Biacabe AG; Streichenberger N; Ironside JW; Mohr M; Kopp N; Perret-Liaudet A
Acta Neuropathol; 2003 Mar; 105(3):296-302. PubMed ID: 12557018
[TBL] [Abstract][Full Text] [Related]
9. A special report I. Prion protein (PrP)--amyloid plaques in the transmissible spongiform encephalopathies, or prion diseases revisited.
Liberski PP; Bratosiewicz J; Waliś A; Kordek R; Jeffrey M; Brown P
Folia Neuropathol; 2001; 39(4):217-35. PubMed ID: 11928893
[TBL] [Abstract][Full Text] [Related]
10. Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease.
Brown P; Gibbs CJ; Rodgers-Johnson P; Asher DM; Sulima MP; Bacote A; Goldfarb LG; Gajdusek DC
Ann Neurol; 1994 May; 35(5):513-29. PubMed ID: 8179297
[TBL] [Abstract][Full Text] [Related]
11. Increased expression of water channel aquaporin 1 and aquaporin 4 in Creutzfeldt-Jakob disease and in bovine spongiform encephalopathy-infected bovine-PrP transgenic mice.
Rodríguez A; Pérez-Gracia E; Espinosa JC; Pumarola M; Torres JM; Ferrer I
Acta Neuropathol; 2006 Nov; 112(5):573-85. PubMed ID: 16871401
[TBL] [Abstract][Full Text] [Related]
12. Gerstmann-Sträussler-Scheinker disease: immunohistological and experimental studies.
Tateishi J; Kitamoto T; Hashiguchi H; Shii H
Ann Neurol; 1988 Jul; 24(1):35-40. PubMed ID: 3046469
[TBL] [Abstract][Full Text] [Related]
13. Amyloid plaques in Creutzfeldt-Jakob disease stain with prion protein antibodies.
Kitamoto T; Tateishi J; Tashima T; Takeshita I; Barry RA; DeArmond SJ; Prusiner SB
Ann Neurol; 1986 Aug; 20(2):204-8. PubMed ID: 3092727
[TBL] [Abstract][Full Text] [Related]
14. Clusterin solubility and aggregation in Creutzfeldt-Jakob disease.
Freixes M; Puig B; Rodríguez A; Torrejón-Escribano B; Blanco R; Ferrer I
Acta Neuropathol; 2004 Oct; 108(4):295-301. PubMed ID: 15235804
[TBL] [Abstract][Full Text] [Related]
15. Distinct immunohistochemical localization in Kuru plaques using novel anti-prion protein antibodies.
Hosokawa T; Ono F; Tsuchiya K; Sato I; Takeyama N; Ueda S; Zanusso G; Takahashi H; Sata T; Sakudo A; Suguira K; Baj A; Toniolo A; Yoshikawa Y; Onodera T
Microbiol Immunol; 2008 Jan; 52(1):25-9. PubMed ID: 18352909
[TBL] [Abstract][Full Text] [Related]
16. Relationship of microglia and scrapie amyloid-immunoreactive plaques in kuru, Creutzfeldt-Jakob disease and Gerstmann-Sträussler syndrome.
Guiroy DC; Wakayama I; Liberski PP; Gajdusek DC
Acta Neuropathol; 1994; 87(5):526-30. PubMed ID: 8059606
[TBL] [Abstract][Full Text] [Related]
17. Advances in the detection of prion protein in peripheral tissues of variant Creutzfeldt-Jakob disease patients using paraffin-embedded tissue blotting.
Ritchie DL; Head MW; Ironside JW
Neuropathol Appl Neurobiol; 2004 Aug; 30(4):360-8. PubMed ID: 15305981
[TBL] [Abstract][Full Text] [Related]
18. A special report I. Prion protein (Prp)--amyloid plaques in the transmissible spongiform encephalopathies (TSEs) or prion disease revisited.
Liberski PP; Bratosiewicz J; Waliś A; Kordek R; Jeffrey M; Brown P
Pol J Pathol; 2001; 52(4):169-86. PubMed ID: 11915178
[TBL] [Abstract][Full Text] [Related]
19. Adenosine A1 receptor protein levels and activity is increased in the cerebral cortex in Creutzfeldt-Jakob disease and in bovine spongiform encephalopathy-infected bovine-PrP mice.
Rodríguez A; Martín M; Albasanz JL; Barrachina M; Espinosa JC; Torres JM; Ferrer I
J Neuropathol Exp Neurol; 2006 Oct; 65(10):964-75. PubMed ID: 17021401
[TBL] [Abstract][Full Text] [Related]
20. Transmission of chronic spongiform encephalopathy with kuru plaques from humans to small rodents.
Tateishi J; Ohta M; Koga M; Sato Y; Kuroiwa Y
Ann Neurol; 1979 Jun; 5(6):581-4. PubMed ID: 382976
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]