172 related articles for article (PubMed ID: 30801763)
1. Accumulation of prion protein in the vagus nerve in creutzfeldt-jakob disease.
Kresl P; Rahimi J; Gelpi E; Aldecoa I; Ricken G; Danics K; Keller E; Kovacs GG
Ann Neurol; 2019 May; 85(5):782-787. PubMed ID: 30801763
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature.
Rossi M; Saverioni D; Di Bari M; Baiardi S; Lemstra AW; Pirisinu L; Capellari S; Rozemuller A; Nonno R; Parchi P
Acta Neuropathol Commun; 2017 Nov; 5(1):87. PubMed ID: 29169405
[TBL] [Abstract][Full Text] [Related]
6. Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease.
Galeno R; Di Bari MA; Nonno R; Cardone F; Sbriccoli M; Graziano S; Ingrosso L; Fiorini M; Valanzano A; Pasini G; Poleggi A; Vinci R; Ladogana A; Puopolo M; Monaco S; Agrimi U; Zanusso G; Pocchiari M
J Virol; 2017 Jun; 91(11):. PubMed ID: 28298604
[TBL] [Abstract][Full Text] [Related]
7. Relative Abundance of apoE and Aβ1-42 Associated with Abnormal Prion Protein Differs between Creutzfeldt-Jakob Disease Subtypes.
Moore RA; Choi YP; Head MW; Ironside JW; Faris R; Ritchie DL; Zanusso G; Priola SA
J Proteome Res; 2016 Dec; 15(12):4518-4531. PubMed ID: 27597180
[TBL] [Abstract][Full Text] [Related]
8. Elevated E200K Somatic Mutation of the Prion Protein Gene (
Won SY; Kim YC; Jeong BH
Int J Mol Sci; 2023 Oct; 24(19):. PubMed ID: 37834279
[TBL] [Abstract][Full Text] [Related]
9. The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients.
Moore RA; Head MW; Ironside JW; Ritchie DL; Zanusso G; Choi YP; Priola SA
PLoS Pathog; 2016 Feb; 12(2):e1005416. PubMed ID: 26840342
[TBL] [Abstract][Full Text] [Related]
10. Synaptic pathology and cell death in the cerebellum in Creutzfeldt-Jakob disease.
Ferrer I
Cerebellum; 2002 Jul; 1(3):213-22. PubMed ID: 12879983
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Development of an Automated Capillary Immunoassay to Detect Prion Glycotypes in Creutzfeldt-Jakob Disease.
Myskiw J; Lamoureux L; Peterson A; Knox D; Jansen GH; Coulthart MB; Booth SA
Lab Invest; 2023 Mar; 103(3):100029. PubMed ID: 36925197
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Classification of sporadic Creutzfeldt-Jakob disease revisited.
Cali I; Castellani R; Yuan J; Al-Shekhlee A; Cohen ML; Xiao X; Moleres FJ; Parchi P; Zou WQ; Gambetti P
Brain; 2006 Sep; 129(Pt 9):2266-77. PubMed ID: 16923954
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Body-first Parkinson's disease and variant Creutzfeldt-Jakob disease - similar or different?
Woerman AL; Tamgüney G
Neurobiol Dis; 2022 Mar; 164():105625. PubMed ID: 35026401
[TBL] [Abstract][Full Text] [Related]
18. Molecular Subtyping of PrP
Klug GM; Lewis V; Collins SJ
Methods Mol Biol; 2017; 1658():347-354. PubMed ID: 28861800
[TBL] [Abstract][Full Text] [Related]
19. Prion Protein-Hemin Interaction Upregulates Hemoglobin Synthesis: Implications for Cerebral Hemorrhage and Sporadic Creutzfeldt-Jakob Disease.
Tripathi AK; Singh N
J Alzheimers Dis; 2016; 51(1):107-21. PubMed ID: 26836195
[TBL] [Abstract][Full Text] [Related]
20. Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone.
Cali I; Miller CJ; Parisi JE; Geschwind MD; Gambetti P; Schonberger LB
Acta Neuropathol Commun; 2015 Jun; 3():37. PubMed ID: 26108478
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
