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.
27. Aggresome formation by mutant prion proteins: the unfolding role of proteasomes in familial prion disorders. Mishra RS; Bose S; Gu Y; Li R; Singh N J Alzheimers Dis; 2003 Feb; 5(1):15-23. PubMed ID: 12590162 [TBL] [Abstract][Full Text] [Related]
28. [Prion diseases in humans]. Zavalishin IA; Roĭkhel' VM; Zhuchenko TD; Shitikova IE Zh Nevrol Psikhiatr Im S S Korsakova; 1998; 98(1):61-6. PubMed ID: 9505410 [No Abstract] [Full Text] [Related]
29. The prion diseases. Brown K; Mastrianni JA J Geriatr Psychiatry Neurol; 2010 Dec; 23(4):277-98. PubMed ID: 20938044 [TBL] [Abstract][Full Text] [Related]
30. [Recent advances in the research of Creutzfeldt-Jakob disease (CJD) and Gerstmann-Strüssler syndrome (GSS)]. Tateishi J Rinsho Shinkeigaku; 1991 Dec; 31(12):1306-8. PubMed ID: 1687809 [TBL] [Abstract][Full Text] [Related]
31. A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene. Liberski PP; Barcikowska M; Cervenakova L; Bratosiewicz J; Marczewska M; Brown P; Gajdusek DC Acta Neuropathol; 1998 Oct; 96(4):425-30. PubMed ID: 9797009 [TBL] [Abstract][Full Text] [Related]
32. [Gene mutation and pathology in human prion disease]. Tashiro H; Doh-ura K No To Shinkei; 1997 Aug; 49(8):681-7. PubMed ID: 9282361 [No Abstract] [Full Text] [Related]
33. A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene. Liberski PP; Bratosiewicz J; Barcikowska M; Cervenakova L; Marczewska M; Brown P; Gajdusek DC Acta Neuropathol; 2000 Aug; 100(2):233-4. PubMed ID: 10963373 [No Abstract] [Full Text] [Related]
34. A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformation. Tunnell E; Wollman R; Mallik S; Cortes CJ; Dearmond SJ; Mastrianni JA Neurology; 2008 Oct; 71(18):1431-8. PubMed ID: 18955686 [TBL] [Abstract][Full Text] [Related]
36. De novo P102L mutation in a patient with Gerstmann-Sträussler-Scheinker disease. Kojović M; Glavač D; Ožek B; Zupan A; Popović M Eur J Neurol; 2011 Dec; 18(12):e152-3. PubMed ID: 22097954 [No Abstract] [Full Text] [Related]
37. Genetics of prion diversity and host susceptibility. Carlson GA Curr Top Microbiol Immunol; 1991; 172():153-64. PubMed ID: 1687380 [No Abstract] [Full Text] [Related]
38. Epitope scanning indicates structural differences in brain-derived monomeric and aggregated mutant prion proteins related to genetic prion diseases. Tapella L; Stravalaci M; Bastone A; Biasini E; Gobbi M; Chiesa R Biochem J; 2013 Sep; 454(3):417-25. PubMed ID: 23808898 [TBL] [Abstract][Full Text] [Related]
39. Prion encephalopathies of animals and humans. Prusiner SB Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114 [TBL] [Abstract][Full Text] [Related]
40. Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations. Miyazono M; Kitamoto T; Doh-ura K; Iwaki T; Tateishi J Acta Neuropathol; 1992; 84(4):349-54. PubMed ID: 1359725 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]