276 related articles for article (PubMed ID: 15741275)
21. Beyond PrP9res) type 1/type 2 dichotomy in Creutzfeldt-Jakob disease.
Uro-Coste E; Cassard H; Simon S; Lugan S; Bilheude JM; Perret-Liaudet A; Ironside JW; Haik S; Basset-Leobon C; Lacroux C; Peoch' K; Streichenberger N; Langeveld J; Head MW; Grassi J; Hauw JJ; Schelcher F; Delisle MB; Andréoletti O
PLoS Pathog; 2008 Mar; 4(3):e1000029. PubMed ID: 18389084
[TBL] [Abstract][Full Text] [Related]
22. Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes.
Ward A; Hollister JR; McNally K; Ritchie DL; Zanusso G; Priola SA
Acta Neuropathol Commun; 2020 Jun; 8(1):83. PubMed ID: 32517816
[TBL] [Abstract][Full Text] [Related]
23. A novel phenotype of sporadic Creutzfeldt-Jakob disease.
Giaccone G; Di Fede G; Mangieri M; Limido L; Capobianco R; Suardi S; Grisoli M; Binelli S; Fociani P; Bugiani O; Tagliavini F
J Neurol Neurosurg Psychiatry; 2007 Dec; 78(12):1379-82. PubMed ID: 18024694
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Neuronal and astrocytic responses involving the serotonergic system in human spongiform encephalopathies.
Fraser E; McDonagh AM; Head M; Bishop M; Ironside JW; Mann DM
Neuropathol Appl Neurobiol; 2003 Oct; 29(5):482-95. PubMed ID: 14507340
[TBL] [Abstract][Full Text] [Related]
26. Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties.
Bishop MT; Will RG; Manson JC
Proc Natl Acad Sci U S A; 2010 Jun; 107(26):12005-10. PubMed ID: 20547859
[TBL] [Abstract][Full Text] [Related]
27. Beyond PrP res type 1/type 2 dichotomy in Creutzfeldt-Jakob disease.
Uro-Coste E; Cassard H; Simon S; Lugan S; Bilheude JM; Perret-Liaudet A; Ironside JW; Haik S; Basset-Leobon C; Lacroux C; Peoch K; Streichenberger N; Langeveld J; Head MW; Grassi J; Hauw JJ; Schelcher F; Delisle MB; Andréoletti O
PLoS Pathog; 2008 Mar; 4(3):e1000029. PubMed ID: 18383623
[TBL] [Abstract][Full Text] [Related]
28. Molecular classification of sporadic Creutzfeldt-Jakob disease.
Hill AF; Joiner S; Wadsworth JD; Sidle KC; Bell JE; Budka H; Ironside JW; Collinge J
Brain; 2003 Jun; 126(Pt 6):1333-46. PubMed ID: 12764055
[TBL] [Abstract][Full Text] [Related]
29. Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypes.
Zanusso G; Farinazzo A; Prelli F; Fiorini M; Gelati M; Ferrari S; Righetti PG; Rizzuto N; Frangione B; Monaco S
J Biol Chem; 2004 Sep; 279(37):38936-42. PubMed ID: 15247220
[TBL] [Abstract][Full Text] [Related]
30. Rapid detection of Creutzfeldt-Jakob disease and scrapie prion proteins.
Serban D; Taraboulos A; DeArmond SJ; Prusiner SB
Neurology; 1990 Jan; 40(1):110-7. PubMed ID: 1967489
[TBL] [Abstract][Full Text] [Related]
31. Distinctive properties of plaque-type dura mater graft-associated Creutzfeldt-Jakob disease in cell-protein misfolding cyclic amplification.
Takeuchi A; Kobayashi A; Parchi P; Yamada M; Morita M; Uno S; Kitamoto T
Lab Invest; 2016 May; 96(5):581-7. PubMed ID: 26878132
[TBL] [Abstract][Full Text] [Related]
32. Sporadic Creutzfeldt-Jakob disease: Real-Time Quaking Induced Conversion (RT-QuIC) assay represents a major diagnostic advance.
Cazzaniga FA; Bistaffa E; De Luca CMG; Bufano G; Indaco A; Giaccone G; Moda F
Eur J Histochem; 2021 Oct; 65(s1):. PubMed ID: 34657408
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease.
Head MW; Northcott V; Rennison K; Ritchie D; McCardle L; Bunn TJ; McLennan NF; Ironside JW; Tullo AB; Bonshek RE
Invest Ophthalmol Vis Sci; 2003 Jan; 44(1):342-6. PubMed ID: 12506094
[TBL] [Abstract][Full Text] [Related]
35. Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice.
Jaumain E; Quadrio I; Herzog L; Reine F; Rezaei H; Andréoletti O; Laude H; Perret-Liaudet A; Haïk S; Béringue V
J Virol; 2016 Dec; 90(23):10867-10874. PubMed ID: 27681129
[TBL] [Abstract][Full Text] [Related]
36. Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrP) associated with variant Creutzfeldt-Jakob disease.
Jones M; Peden AH; Yull H; Wight D; Bishop MT; Prowse CV; Turner ML; Ironside JW; MacGregor IR; Head MW
Transfusion; 2009 Feb; 49(2):376-84. PubMed ID: 18980616
[TBL] [Abstract][Full Text] [Related]
37. A traceback phenomenon can reveal the origin of prion infection.
Kobayashi A; Asano M; Mohri S; Kitamoto T
Neuropathology; 2009 Oct; 29(5):619-24. PubMed ID: 19659941
[TBL] [Abstract][Full Text] [Related]
38. Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease.
Castellani RJ; Colucci M; Xie Z; Zou W; Li C; Parchi P; Capellari S; Pastore M; Rahbar MH; Chen SG; Gambetti P
Neurology; 2004 Aug; 63(3):436-42. PubMed ID: 15304573
[TBL] [Abstract][Full Text] [Related]
39. Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.
Faucheux BA; Morain E; Diouron V; Brandel JP; Salomon D; Sazdovitch V; Privat N; Laplanche JL; Hauw JJ; Haïk S
Neuropathol Appl Neurobiol; 2011 Aug; 37(5):500-12. PubMed ID: 21450052
[TBL] [Abstract][Full Text] [Related]
40. A patient with MV2 subtype of sporadic Creutzfeldt-Jakob disease and atypical clinical presentation.
Guerrero D; Martínez-Velilla N; Caballero MC; Mendióroz MT; Tuñón T; Masdeu J; Rodríguez A; Armstrong J; Ferrer I
Clin Neuropathol; 2008; 27(6):408-13. PubMed ID: 19130739
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]