182 related articles for article (PubMed ID: 1684757)
1. PrP amyloid plaques in Creutzfeldt-Jakob disease of short duration: immunohistochemical studies of 5 cases from Poland.
Liberski PP; Kwiecinski H; Barcikowska M; Mirecka B; Kulczycki J; Kida E; Brown P; Gajdusek DC
Eur J Epidemiol; 1991 Sep; 7(5):505-10. PubMed ID: 1684757
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. [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]
5. The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease.
Di Fede G; Giaccone G; Limido L; Mangieri M; Suardi S; Puoti G; Morbin M; Mazzoleni G; Ghetti B; Tagliavini F
J Neuropathol Exp Neurol; 2007 Feb; 66(2):124-30. PubMed ID: 17278997
[TBL] [Abstract][Full Text] [Related]
6. Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.
Zanusso G; Fiorini M; Ferrari S; Meade-White K; Barbieri I; Brocchi E; Ghetti B; Monaco S
J Biol Chem; 2014 Feb; 289(8):4870-81. PubMed ID: 24398683
[TBL] [Abstract][Full Text] [Related]
7. A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation.
Miyazono M; Iwaki T; Kitamoto T; Kaneko Y; Doh-ura K; Tateishi J
Am J Pathol; 1991 Sep; 139(3):589-98. PubMed ID: 1679596
[TBL] [Abstract][Full Text] [Related]
8. A prion protein missense variant is integrated in kuru plaque cores in patients with Gerstmann-Sträussler syndrome.
Kitamoto T; Yamaguchi K; Doh-ura K; Tateishi J
Neurology; 1991 Feb; 41(2 ( Pt 1)):306-10. PubMed ID: 1671530
[TBL] [Abstract][Full Text] [Related]
9. Ultrastructural study of florid plaques in variant Creutzfeldt-Jakob disease: a comparison with amyloid plaques in kuru, sporadic Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease.
Sikorska B; Liberski PP; Sobów T; Budka H; Ironside JW
Neuropathol Appl Neurobiol; 2009 Feb; 35(1):46-59. PubMed ID: 18513219
[TBL] [Abstract][Full Text] [Related]
10. Diffuse deposition of immunohistochemically labeled prion protein in the granular layer of the cerebellum in a patient with Creutzfeldt-Jakob disease.
Kretzschmar HA; Kitamoto T; Doerr-Schott J; Mehraein P; Tateishi J
Acta Neuropathol; 1991; 82(6):536-40. PubMed ID: 1686132
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Colocalization of prion protein and beta protein in the same amyloid plaques in patients with Gerstmann-Sträussler syndrome.
Miyazono M; Kitamoto T; Iwaki T; Tateishi J
Acta Neuropathol; 1992; 83(4):333-9. PubMed ID: 1349451
[TBL] [Abstract][Full Text] [Related]
13. Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations.
Miyazono M; Kitamoto T; Doh-ura K; Iwaki T; Tateishi J
Acta Neuropathol; 1992; 84(4):349-54. PubMed ID: 1359725
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Localization of disease-related PrP in Danish patients with different subtypes of prion disease.
Bergström AL; Heegaard PM; Dyrbye H; Lind P; Laursen H
Clin Neuropathol; 2009; 28(5):321-32. PubMed ID: 19788047
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Creutzfeldt-Jakob disease with Alzheimer-type A beta-reactive amyloid plaques.
Barcikowska M; Kwiecinski H; Liberski PP; Kowalski J; Brown P; Gajdusek DC
Histopathology; 1995 May; 26(5):445-50. PubMed ID: 7657313
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Immunohistochemical investigations of the prion protein accumulation in human spongiform encephalopathies. Special report II.
Zaborowski A; Kordek R; Botts GT; Liberski PP
Pol J Pathol; 2003; 54(1):39-47. PubMed ID: 12817879
[TBL] [Abstract][Full Text] [Related]
20. Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred).
Piccardo P; Seiler C; Dlouhy SR; Young K; Farlow MR; Prelli F; Frangione B; Bugiani O; Tagliavini F; Ghetti B
J Neuropathol Exp Neurol; 1996 Nov; 55(11):1157-63. PubMed ID: 8939199
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
