These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

334 related articles for article (PubMed ID: 9833398)

  • 1. The evolution of views on the nosological position of transmissible spongiform encephalopathies.
    Liberski PP; Brown P; Gajdusek CD
    Folia Neuropathol; 1997; 35(4):214-25. PubMed ID: 9833398
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The prion diseases.
    Mastrianni JA; Roos RP
    Semin Neurol; 2000; 20(3):337-52. PubMed ID: 11051298
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [A trend of molecular genetics on prion diseases and prion protein].
    Muramatsu Y; Shinagawa M
    Nihon Rinsho; 1993 Sep; 51(9):2494-502. PubMed ID: 8411733
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The human spongiform encephalopathies: kuru, Creutzfeldt-Jakob disease, and the Gerstmann-Sträussler-Scheinker syndrome.
    Brown P; Gajdusek DC
    Curr Top Microbiol Immunol; 1991; 172():1-20. PubMed ID: 1687378
    [No Abstract]   [Full Text] [Related]  

  • 5. Neuropathology of human prion diseases (spongiform encephalopathies).
    Kretzschmar HA
    Dev Biol Stand; 1993; 80():71-90. PubMed ID: 8270118
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. "Life, Jim, but not as we know it"? Transmissible dementias and the prion protein.
    Harrison PJ; Roberts GW
    Br J Psychiatry; 1991 Apr; 158():457-70. PubMed ID: 2054560
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The diagnosis of human prion diseases.
    Kordek R
    Folia Neuropathol; 2000; 38(4):151-60. PubMed ID: 11693717
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new point mutation of the PRNP gene in Gerstmann-Sträussler-Scheinker case in Poland.
    Bratosiewicz J; Barcikowska M; Cervenakowa L; Brown P; Gajdusek DC; Liberski PP
    Folia Neuropathol; 2000; 38(4):164-6. PubMed ID: 11693719
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The molecular biology of the transmissible dementias.
    Owen F
    Mol Cell Biol Hum Dis Ser; 1994; 4():110-32. PubMed ID: 9439746
    [No Abstract]   [Full Text] [Related]  

  • 11. An overview of human prion diseases.
    Imran M; Mahmood S
    Virol J; 2011 Dec; 8():559. PubMed ID: 22196171
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. The prion diseases.
    Brown K; Mastrianni JA
    J Geriatr Psychiatry Neurol; 2010 Dec; 23(4):277-98. PubMed ID: 20938044
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Transmissible spongiform encephalopathies. History, epidemiology, etiological, hyphotheses].
    Gargani G
    Minerva Med; 2002 Feb; 93(1):59-73. PubMed ID: 11850614
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Prion diseases in humans].
    Zavalishin IA; Roĭkhel' VM; Zhuchenko TD; Shitikova IE
    Zh Nevrol Psikhiatr Im S S Korsakova; 1998; 98(1):61-6. PubMed ID: 9505410
    [No Abstract]   [Full Text] [Related]  

  • 16. Transmissible spongiform encephalopathies and human neurodegenerative disease.
    Esmonde TF; Will RG
    Br J Hosp Med; 1993 Mar 17-Apr 6; 49(6):400-4, 406. PubMed ID: 8472098
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The spongiform encephalopathies.
    Will RG
    J Neurol Neurosurg Psychiatry; 1991 Sep; 54(9):761-3. PubMed ID: 1955893
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene.
    Liberski PP; Bratosiewicz J; Barcikowska M; Cervenakova L; Marczewska M; Brown P; Gajdusek DC
    Acta Neuropathol; 2000 Aug; 100(2):233-4. PubMed ID: 10963373
    [No Abstract]   [Full Text] [Related]  

  • 20. The nosology of Creutzfeldt-Jakob disease and conditions related to the accumulation of PrPCJD in the nervous system.
    Richardson EP; Masters CL
    Brain Pathol; 1995 Jan; 5(1):33-41. PubMed ID: 7767489
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.