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.
174 related articles for article (PubMed ID: 35215959)
1. 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]
2. A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report. Rodríguez-Martínez AB; Garrido JM; Zarranz JJ; Arteagoitia JM; de Pancorbo MM; Atarés B; Bilbao MJ; Ferrer I; Juste RA BMC Neurol; 2010 Oct; 10():99. PubMed ID: 20973975 [TBL] [Abstract][Full Text] [Related]
3. The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt-Jakob disease. Peden AH; Sarode DP; Mulholland CR; Barria MA; Ritchie DL; Ironside JW; Head MW Acta Neuropathol Commun; 2014 Oct; 2():152. PubMed ID: 25331173 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
10. 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]
11. In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrP Wang Z; Yuan J; Shen P; Abskharon R; Lang Y; Dang J; Adornato A; Xu L; Chen J; Feng J; Moudjou M; Kitamoto T; Lee HG; Kim YS; Langeveld J; Appleby B; Ma J; Kong Q; Petersen RB; Zou WQ; Cui L Mol Neurobiol; 2019 Aug; 56(8):5456-5469. PubMed ID: 30612334 [TBL] [Abstract][Full Text] [Related]
12. Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. Zou WQ; Puoti G; Xiao X; Yuan J; Qing L; Cali I; Shimoji M; Langeveld JP; Castellani R; Notari S; Crain B; Schmidt RE; Geschwind M; Dearmond SJ; Cairns NJ; Dickson D; Honig L; Torres JM; Mastrianni J; Capellari S; Giaccone G; Belay ED; Schonberger LB; Cohen M; Perry G; Kong Q; Parchi P; Tagliavini F; Gambetti P Ann Neurol; 2010 Aug; 68(2):162-72. PubMed ID: 20695009 [TBL] [Abstract][Full Text] [Related]
13. Pathologic and biochemical characterization of PrP Moore SJ; Vrentas CE; Hwang S; West Greenlee MH; Nicholson EM; Greenlee JJ BMC Vet Res; 2018 Mar; 14(1):80. PubMed ID: 29523205 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD. Pastore M; Chin SS; Bell KL; Dong Z; Yang Q; Yang L; Yuan J; Chen SG; Gambetti P; Zou WQ Am J Pathol; 2005 Dec; 167(6):1729-38. PubMed ID: 16314483 [TBL] [Abstract][Full Text] [Related]
16. Small ruminant nor98 prions share biochemical features with human gerstmann-sträussler-scheinker disease and variably protease-sensitive prionopathy. Pirisinu L; Nonno R; Esposito E; Benestad SL; Gambetti P; Agrimi U; Zou WQ PLoS One; 2013; 8(6):e66405. PubMed ID: 23826096 [TBL] [Abstract][Full Text] [Related]
17. An autopsy case of variably protease-sensitive prionopathy with Met/Met homogeneity at codon 129. Uchino A; Saito Y; Oonuma S; Murayama S; Yagishita S; Kitamoto T; Hasegawa K Neuropathology; 2023 Dec; 43(6):486-495. PubMed ID: 37253452 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Further Characterization of Glycoform-Selective Prions of Variably Protease-Sensitive Prionopathy. Zhang W; Xiao X; Ding M; Yuan J; Foutz A; Moudjou M; Kitamoto T; Langeveld JPM; Cui L; Zou WQ Pathogens; 2021 Apr; 10(5):. PubMed ID: 33922765 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]