171 related articles for article (PubMed ID: 38651736)
1. Prion meeting 2023: implications of a growing field.
Outeiro TF; Vieira TCRG
Prion; 2024 Dec; 18(1):68-71. PubMed ID: 38651736
[TBL] [Abstract][Full Text] [Related]
2. Human transmissible spongiform encephalopathies: historic view.
Asher DM; Gregori L
Handb Clin Neurol; 2018; 153():1-17. PubMed ID: 29887130
[TBL] [Abstract][Full Text] [Related]
3. [Prion diseases or transmissible spongiform encephalopathies].
Brandel JP
Rev Med Interne; 2022 Feb; 43(2):106-115. PubMed ID: 34148672
[TBL] [Abstract][Full Text] [Related]
4. How an Infection of Sheep Revealed Prion Mechanisms in Alzheimer's Disease and Other Neurodegenerative Disorders.
Carlson GA; Prusiner SB
Int J Mol Sci; 2021 May; 22(9):. PubMed ID: 34064393
[TBL] [Abstract][Full Text] [Related]
5. The kuru infectious agent is a unique geographic isolate distinct from Creutzfeldt-Jakob disease and scrapie agents.
Manuelidis L; Chakrabarty T; Miyazawa K; Nduom NA; Emmerling K
Proc Natl Acad Sci U S A; 2009 Aug; 106(32):13529-34. PubMed ID: 19633190
[TBL] [Abstract][Full Text] [Related]
6. Molecular biology and pathology of scrapie and the prion diseases of humans.
Prusiner SB; DeArmond SJ
Brain Pathol; 1991 Jul; 1(4):297-310. PubMed ID: 1669719
[TBL] [Abstract][Full Text] [Related]
7. Human prion diseases: from Kuru to variant Creutzfeldt-Jakob disease.
Sikorska B; Liberski PP
Subcell Biochem; 2012; 65():457-96. PubMed ID: 23225013
[TBL] [Abstract][Full Text] [Related]
8. [Encephalopathy caused by prions].
Michel B
Rev Neurol (Paris); 1990; 146(1):1-11. PubMed ID: 2408126
[TBL] [Abstract][Full Text] [Related]
9. Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice.
Wadsworth JD; Joiner S; Linehan JM; Desbruslais M; Fox K; Cooper S; Cronier S; Asante EA; Mead S; Brandner S; Hill AF; Collinge J
Proc Natl Acad Sci U S A; 2008 Mar; 105(10):3885-90. PubMed ID: 18316717
[TBL] [Abstract][Full Text] [Related]
10. Analysis of Conformational Stability of Abnormal Prion Protein Aggregates across the Spectrum of Creutzfeldt-Jakob Disease Prions.
Cescatti M; Saverioni D; Capellari S; Tagliavini F; Kitamoto T; Ironside J; Giese A; Parchi P
J Virol; 2016 Jul; 90(14):6244-6254. PubMed ID: 27122583
[TBL] [Abstract][Full Text] [Related]
11. Prion disease: a tale of folds and strains.
Kretzschmar H; Tatzelt J
Brain Pathol; 2013 May; 23(3):321-32. PubMed ID: 23587138
[TBL] [Abstract][Full Text] [Related]
12. Genetic and infectious prion diseases.
Prusiner SB
Arch Neurol; 1993 Nov; 50(11):1129-53. PubMed ID: 8105771
[TBL] [Abstract][Full Text] [Related]
13. Similarities between forms of sheep scrapie and Creutzfeldt-Jakob disease are encoded by distinct prion types.
Wemheuer WM; Benestad SL; Wrede A; Schulze-Sturm U; Wemheuer WE; Hahmann U; Gawinecka J; Schütz E; Zerr I; Brenig B; Bratberg B; Andréoletti O; Schulz-Schaeffer WJ
Am J Pathol; 2009 Dec; 175(6):2566-73. PubMed ID: 19850886
[TBL] [Abstract][Full Text] [Related]
14. Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.
Parchi P; Cescatti M; Notari S; Schulz-Schaeffer WJ; Capellari S; Giese A; Zou WQ; Kretzschmar H; Ghetti B; Brown P
Brain; 2010 Oct; 133(10):3030-42. PubMed ID: 20823086
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Scrapie and Creutzfeldt-Jakob disease prion proteins share physical properties and antigenic determinants.
Bendheim PE; Bockman JM; McKinley MP; Kingsbury DT; Prusiner SB
Proc Natl Acad Sci U S A; 1985 Feb; 82(4):997-1001. PubMed ID: 2579394
[TBL] [Abstract][Full Text] [Related]
17. Human prion diseases: surgical lessons learned from iatrogenic prion transmission.
Bonda DJ; Manjila S; Mehndiratta P; Khan F; Miller BR; Onwuzulike K; Puoti G; Cohen ML; Schonberger LB; Cali I
Neurosurg Focus; 2016 Jul; 41(1):E10. PubMed ID: 27364252
[TBL] [Abstract][Full Text] [Related]
18. Defining the phenotypic spectrum of sporadic Creutzfeldt-Jakob disease MV2K: the kuru plaque type.
Baiardi S; Mammana A; Dellavalle S; Rossi M; Redaelli V; Colaizzo E; Di Fede G; Ladogana A; Capellari S; Parchi P
Brain; 2023 Aug; 146(8):3289-3300. PubMed ID: 36883639
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases.
Kobayashi A; Parchi P; Yamada M; Mohri S; Kitamoto T
Neuropathology; 2016 Jun; 36(3):305-10. PubMed ID: 26669818
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
