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.
328 related articles for article (PubMed ID: 18571782)
21. Protease-sensitive prions with 144-bp insertion mutations. Xiao X; Cali I; Dong Z; Puoti G; Yuan J; Qing L; Wang H; Kong Q; Gambetti P; Zou WQ Aging (Albany NY); 2013 Mar; 5(3):155-73. PubMed ID: 23515139 [TBL] [Abstract][Full Text] [Related]
22. Contribution of neuropathology to the understanding of human prion disease. Kovács GG; Kalev O; Budka H Folia Neuropathol; 2004; 42 Suppl A():69-76. PubMed ID: 15449461 [TBL] [Abstract][Full Text] [Related]
29. Variably protease-sensitive prionopathy with methionine homozygosity at codon 129 in the prion protein gene. Clemmensen FK; Areskeviciute A; Lund EL; Roos P BMJ Case Rep; 2024 Feb; 17(2):. PubMed ID: 38388201 [TBL] [Abstract][Full Text] [Related]
30. Development of oligomeric prion-protein aggregates in a mouse model of prion disease. Sasaki K; Minaki H; Iwaki T J Pathol; 2009 Sep; 219(1):123-30. PubMed ID: 19479969 [TBL] [Abstract][Full Text] [Related]
32. Phenotypic Heterogeneity of Variably Protease-Sensitive Prionopathy: A Report of Three Cases Carrying Different Genotypes at Baiardi S; Mammana A; Rossi M; Ladogana A; Carlà B; Gambetti P; Capellari S; Parchi P Viruses; 2022 Feb; 14(2):. PubMed ID: 35215959 [TBL] [Abstract][Full Text] [Related]
33. Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia. Parchi P; Capellari S; Gambetti P Microsc Res Tech; 2000 Jul; 50(1):16-25. PubMed ID: 10871544 [TBL] [Abstract][Full Text] [Related]
34. In vitro amplification of scrapie and chronic wasting disease PrP(res) using baculovirus-expressed recombinant PrP as substrate. Faburay B; Tark D; Kanthasamy AG; Richt JA Prion; 2014; 8(6):393-403. PubMed ID: 25495764 [TBL] [Abstract][Full Text] [Related]
35. The first case of protease-sensitive prionopathy (PSPr) in The Netherlands: a patient with an unusual GSS-like clinical phenotype. Jansen C; Head MW; van Gool WA; Baas F; Yull H; Ironside JW; Rozemuller AJ J Neurol Neurosurg Psychiatry; 2010 Sep; 81(9):1052-5. PubMed ID: 20547632 [TBL] [Abstract][Full Text] [Related]
36. Prion Protein Devoid of the Octapeptide Repeat Region Delays Bovine Spongiform Encephalopathy Pathogenesis in Mice. Hara H; Miyata H; Das NR; Chida J; Yoshimochi T; Uchiyama K; Watanabe H; Kondoh G; Yokoyama T; Sakaguchi S J Virol; 2018 Jan; 92(1):. PubMed ID: 29046443 [TBL] [Abstract][Full Text] [Related]
37. Protease-sensitive prion species in neoplastic spleens of prion-infected mice with uncoupling of PrP(Sc) and prion infectivity. Krasemann S; Neumann M; Szalay B; Stocking C; Glatzel M J Gen Virol; 2013 Feb; 94(Pt 2):453-463. PubMed ID: 23136363 [TBL] [Abstract][Full Text] [Related]
38. Real and imagined clinicopathological limits of "prion dementia". Brown P; Kaur P; Sulima MP; Goldfarb LG; Gibbs CJ; Gajdusek DC Lancet; 1993 Jan; 341(8838):127-9. PubMed ID: 8093741 [TBL] [Abstract][Full Text] [Related]
39. Fatal transmissible amyloid encephalopathy: a new type of prion disease associated with lack of prion protein membrane anchoring. Chesebro B; Race B; Meade-White K; Lacasse R; Race R; Klingeborn M; Striebel J; Dorward D; McGovern G; Jeffrey M PLoS Pathog; 2010 Mar; 6(3):e1000800. PubMed ID: 20221436 [TBL] [Abstract][Full Text] [Related]
40. Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States. Notari S; Moleres FJ; Hunter SB; Belay ED; Schonberger LB; Cali I; Parchi P; Shieh WJ; Brown P; Zaki S; Zou WQ; Gambetti P PLoS One; 2010 Jan; 5(1):e8765. PubMed ID: 20098730 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]