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2. 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. 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]
5. Transmissible spongiform encephalopathies in humans: kuru, Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease. Brown P Can J Vet Res; 1990 Jan; 54(1):38-41. PubMed ID: 2407329 [No Abstract] [Full Text] [Related]
6. Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies. Collins S; McLean CA; Masters CL J Clin Neurosci; 2001 Sep; 8(5):387-97. PubMed ID: 11535002 [TBL] [Abstract][Full Text] [Related]
7. Clinical significance of types of cerebellar amyloid plaques in human spongiform encephalopathies. Pearlman RL; Towfighi J; Pezeshkpour GH; Tenser RB; Turel AP Neurology; 1988 Aug; 38(8):1249-54. PubMed ID: 3041312 [TBL] [Abstract][Full Text] [Related]
8. 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]
12. Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome. Goldfarb LG; Brown P; Goldgaber D; Asher DM; Rubenstein R; Brown WT; Piccardo P; Kascsak RJ; Boellaard JW; Gajdusek DC Exp Neurol; 1990 Jun; 108(3):247-50. PubMed ID: 2190844 [TBL] [Abstract][Full Text] [Related]
13. [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]
14. Neuropathology of human prion diseases (spongiform encephalopathies). Kretzschmar HA Dev Biol Stand; 1993; 80():71-90. PubMed ID: 8270118 [TBL] [Abstract][Full Text] [Related]
15. The presence of complements in amyloid plaques of Creutzfeldt-Jakob disease and Gerstmann-Straussler-Scheinker disease. Ishii T; Haga S; Yagishita S; Tateishi J Appl Pathol; 1984; 2(6):370-9. PubMed ID: 6400466 [TBL] [Abstract][Full Text] [Related]
16. From slow virus to prion: a review of transmissible spongiform encephalopathies. Lantos PL Histopathology; 1992 Jan; 20(1):1-11. PubMed ID: 1531331 [TBL] [Abstract][Full Text] [Related]
17. [Subacute spongiform encephalopathy with Kuru-like plaques--comparison with Gerstmann-Sträussler-Scheinker disease]. Tomi H; Sunohara N; Mukoyama M; Ando K; Satoyoshi E Rinsho Shinkeigaku; 1984 Apr; 24(4):367-70. PubMed ID: 6744759 [No Abstract] [Full Text] [Related]
18. Gerstmann-Sträussler-Scheinker disease with A117V mutation in a second French-Alsatian family. Heldt N; Boellaard JW; Brown P; Cervenákova L; Doerr-Schott J; Thomas C; Scherer C; Rohmer F Clin Neuropathol; 1998; 17(4):229-34. PubMed ID: 9707339 [TBL] [Abstract][Full Text] [Related]
19. Gerstmann-Sträussler-Scheinker disease: autopsy study of a familial case. Vinters HV; Hudson AJ; Kaufmann JC Ann Neurol; 1986 Oct; 20(4):540-3. PubMed ID: 3789669 [TBL] [Abstract][Full Text] [Related]