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.
364 related articles for article (PubMed ID: 32517816)
21. Association of an 11-12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt-Jakob disease and other prion diseases. Satoh K; Muramoto T; Tanaka T; Kitamoto N; Ironside JW; Nagashima K; Yamada M; Sato T; Mohri S; Kitamoto T J Gen Virol; 2003 Oct; 84(Pt 10):2885-2893. PubMed ID: 13679624 [TBL] [Abstract][Full Text] [Related]
22. The prion protein preference of sporadic Creutzfeldt-Jakob disease subtypes. Klemm HM; Welton JM; Masters CL; Klug GM; Boyd A; Hill AF; Collins SJ; Lawson VA J Biol Chem; 2012 Oct; 287(43):36465-72. PubMed ID: 22930754 [TBL] [Abstract][Full Text] [Related]
23. Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British woman. Mead S; Joiner S; Desbruslais M; Beck JA; O'Donoghue M; Lantos P; Wadsworth JD; Collinge J Arch Neurol; 2007 Dec; 64(12):1780-4. PubMed ID: 18071044 [TBL] [Abstract][Full Text] [Related]
24. Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002. Head MW; Bunn TJ; Bishop MT; McLoughlin V; Lowrie S; McKimmie CS; Williams MC; McCardle L; MacKenzie J; Knight R; Will RG; Ironside JW Ann Neurol; 2004 Jun; 55(6):851-9. PubMed ID: 15174020 [TBL] [Abstract][Full Text] [Related]
25. Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutation. Watts JC; Giles K; Serban A; Patel S; Oehler A; Bhardwaj S; Guan S; Greicius MD; Miller BL; DeArmond SJ; Geschwind MD; Prusiner SB Ann Neurol; 2015 Oct; 78(4):540-53. PubMed ID: 26094969 [TBL] [Abstract][Full Text] [Related]
28. A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule. Notari S; Capellari S; Langeveld J; Giese A; Strammiello R; Gambetti P; Kretzschmar HA; Parchi P Lab Invest; 2007 Nov; 87(11):1103-12. PubMed ID: 17893675 [TBL] [Abstract][Full Text] [Related]
29. Lack of prion infectivity in fixed heart tissue from patients with Creutzfeldt-Jakob disease or amyloid heart disease. Priola SA; Ward AE; McCall SA; Trifilo M; Choi YP; Solforosi L; Williamson RA; Cruite JT; Oldstone MB J Virol; 2013 Sep; 87(17):9501-10. PubMed ID: 23785217 [TBL] [Abstract][Full Text] [Related]
30. Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain. Puoti G; Giaccone G; Rossi G; Canciani B; Bugiani O; Tagliavini F Neurology; 1999 Dec; 53(9):2173-6. PubMed ID: 10599800 [TBL] [Abstract][Full Text] [Related]
31. Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years. Rudge P; Jaunmuktane Z; Adlard P; Bjurstrom N; Caine D; Lowe J; Norsworthy P; Hummerich H; Druyeh R; Wadsworth JD; Brandner S; Hyare H; Mead S; Collinge J Brain; 2015 Nov; 138(Pt 11):3386-99. PubMed ID: 26268531 [TBL] [Abstract][Full Text] [Related]
32. Prion protein with an E200K mutation displays properties similar to those of the cellular isoform PrP(C). Rosenmann H; Talmor G; Halimi M; Yanai A; Gabizon R; Meiner Z J Neurochem; 2001 Mar; 76(6):1654-62. PubMed ID: 11259483 [TBL] [Abstract][Full Text] [Related]
33. Correlation of polydispersed prion protein and characteristic pathology in the thalamus in variant Creutzfeldt-Jakob disease: implication of small oligomeric species. Choi YP; Gröner A; Ironside JW; Head MW Brain Pathol; 2011 May; 21(3):298-307. PubMed ID: 21029243 [TBL] [Abstract][Full Text] [Related]
34. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases. Schmitz M; Lüllmann K; Zafar S; Ebert E; Wohlhage M; Oikonomou P; Schlomm M; Mitrova E; Beekes M; Zerr I Neurobiol Aging; 2014 May; 35(5):1177-88. PubMed ID: 24360565 [TBL] [Abstract][Full Text] [Related]
35. Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification. Parchi P; Strammiello R; Notari S; Giese A; Langeveld JP; Ladogana A; Zerr I; Roncaroli F; Cras P; Ghetti B; Pocchiari M; Kretzschmar H; Capellari S Acta Neuropathol; 2009 Nov; 118(5):659-71. PubMed ID: 19718500 [TBL] [Abstract][Full Text] [Related]
36. Creutzfeldt-Jakob disease and inclusion body myositis: abundant disease-associated prion protein in muscle. Kovacs GG; Lindeck-Pozza E; Chimelli L; Araújo AQ; Gabbai AA; Ströbel T; Glatzel M; Aguzzi A; Budka H Ann Neurol; 2004 Jan; 55(1):121-5. PubMed ID: 14705121 [TBL] [Abstract][Full Text] [Related]
38. Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene. Di Fede G; Catania M; Atzori C; Moda F; Pasquali C; Indaco A; Grisoli M; Zuffi M; Guaita MC; Testi R; Taraglio S; Sessa M; Gusmaroli G; Spinelli M; Salzano G; Legname G; Tarletti R; Godi L; Pocchiari M; Tagliavini F; Imperiale D; Giaccone G Acta Neuropathol Commun; 2019 Jan; 7(1):1. PubMed ID: 30606247 [TBL] [Abstract][Full Text] [Related]
39. Re-assessment of PrP(Sc) distribution in sporadic and variant CJD. Rubenstein R; Chang B PLoS One; 2013; 8(7):e66352. PubMed ID: 23843953 [TBL] [Abstract][Full Text] [Related]
40. Coexistence of multiple PrPSc types in individuals with Creutzfeldt-Jakob disease. Polymenidou M; Stoeck K; Glatzel M; Vey M; Bellon A; Aguzzi A Lancet Neurol; 2005 Dec; 4(12):805-14. PubMed ID: 16297838 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]