368 related articles for article (PubMed ID: 9157343)
1. [Prion dementias: nosology and diagnostic difficulties in the spectrum of Creutzfeld-Jakob encephalopathy].
Kálmán J; Járdánházy T; Cserháti A; Szekeres G; Demeter I; Berek I; Dobranovics I; Csernay L; Janka Z
Orv Hetil; 1997 Mar; 138(12):731-7. PubMed ID: 9157343
[TBL] [Abstract][Full Text] [Related]
2. [Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Part I].
Zaborowski A
Psychiatr Pol; 2004; 38(2):283-96. PubMed ID: 15307293
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. [Psychiatric manifestations of a new variant of Creutzfeldt-Jakob disease. Apropos of a case].
Dervaux A; Vicart S; Lopes F; Le Borgne MH
Encephale; 2001; 27(2):194-7. PubMed ID: 11407273
[TBL] [Abstract][Full Text] [Related]
5. [Creutzfeldt-Jakob disease(CJD) and Gerstmann-Sträussler-Scheinker syndrome(GSS)].
Udaka F; Fujisawa M; Kameyama M
Nihon Rinsho; 1997 Apr; 55(4):972-7. PubMed ID: 9103904
[TBL] [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 presentations of spongiform encephalopathies in humans].
Szczudlik A; Słowik A
Przegl Lek; 1999; 56(4):324-6. PubMed ID: 10494174
[TBL] [Abstract][Full Text] [Related]
8. The human prion diseases. A review with special emphasis on new variant CJD and comments on surveillance.
Keohane C
Clin Exp Pathol; 1999; 47(3-4):125-32. PubMed ID: 10472732
[TBL] [Abstract][Full Text] [Related]
9. [Creutzfeldt-Jakob disease--a human prion disease].
Buchwald E; Vorstrup S
Nord Med; 1996 Jun; 111(6):180-3. PubMed ID: 8700643
[TBL] [Abstract][Full Text] [Related]
10. [Prions, infections and confusions in the "transmissible" spongiform encephalopathies. The other evidence-based science. III. Review].
León-S FE; Rodriguez CI; Prada DG
Invest Clin; 2000 Sep; 41(3):189-210. PubMed ID: 11029835
[TBL] [Abstract][Full Text] [Related]
11. [Human spongiform encephalopathies. Diseases caused by prions].
Jørn N; Hansen D; Hansen NJ
Ugeskr Laeger; 1996 Jul; 158(28):4066-72. PubMed ID: 8701521
[TBL] [Abstract][Full Text] [Related]
12. The many faces of human prion diseases in Belgium and the world.
Van Everbroeck B; Pals P; Quoilin S; Martin JJ; Cras P
Acta Neurol Belg; 2001 Jun; 101(2):81-7. PubMed ID: 11486562
[TBL] [Abstract][Full Text] [Related]
13. Tubulovesicular structures are a consistent (and unexplained) finding in the brains of humans with prion diseases.
Liberski PP; Sikorska B; Hauw JJ; Kopp N; Streichenberger N; Giraud P; Budka H; Boellaard JW; Brown P
Virus Res; 2008 Mar; 132(1-2):226-8. PubMed ID: 18164506
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. [Surveillance of prion diseases in Japan: analysis of 409 patients].
Yamada M
Rinsho Shinkeigaku; 2003 Nov; 43(11):806-9. PubMed ID: 15152470
[TBL] [Abstract][Full Text] [Related]
17. [Prion diseases in Japan: analysis of 918 patients].
Yamada M
Rinsho Shinkeigaku; 2007 Nov; 47(11):805-8. PubMed ID: 18210803
[TBL] [Abstract][Full Text] [Related]
18. Familial spongiform encephalopathy associated with a novel prion protein gene mutation.
Nitrini R; Rosemberg S; Passos-Bueno MR; da Silva LS; Iughetti P; Papadopoulos M; Carrilho PM; Caramelli P; Albrecht S; Zatz M; LeBlanc A
Ann Neurol; 1997 Aug; 42(2):138-46. PubMed ID: 9266722
[TBL] [Abstract][Full Text] [Related]
19. [Familial prion disease (GSS, familial CJD, FFI)].
Arata H; Takashima H
Nihon Rinsho; 2007 Aug; 65(8):1433-7. PubMed ID: 17695280
[TBL] [Abstract][Full Text] [Related]
20. [Interesting not only as differential Alzheimer dementia diagnosis. Bovine spongiform encephalopathy and other prion diseases].
Kretzschmar H
MMW Fortschr Med; 2000 Sep; 142(39):34-8. PubMed ID: 11072695
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
