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.
200 related articles for article (PubMed ID: 22763467)
1. A novel mutation I215V in the PRNP gene associated with Creutzfeldt-Jakob and Alzheimer's diseases in three patients with divergent clinical phenotypes. Muñoz-Nieto M; Ramonet N; López-Gastón JI; Cuadrado-Corrales N; Calero O; Díaz-Hurtado M; Ipiens JR; Ramón y Cajal S; de Pedro-Cuesta J; Calero M J Neurol; 2013 Jan; 260(1):77-84. PubMed ID: 22763467 [TBL] [Abstract][Full Text] [Related]
2. Creutzfeldt-Jakob disease with PRNP G114V mutation in a Chinese family. Liu Z; Jia L; Piao Y; Lu D; Wang F; Lv H; Lu Y; Jia J Acta Neurol Scand; 2010 Jun; 121(6):377-83. PubMed ID: 20028338 [TBL] [Abstract][Full Text] [Related]
3. Novel prion protein gene mutation in an octogenarian with Creutzfeldt-Jakob disease. Collins S; Boyd A; Fletcher A; Byron K; Harper C; McLean CA; Masters CL Arch Neurol; 2000 Jul; 57(7):1058-63. PubMed ID: 10891990 [TBL] [Abstract][Full Text] [Related]
4. Novel prion protein gene mutation at codon 196 (E196A) in a septuagenarian with Creutzfeldt-Jakob disease. Zhang H; Wang M; Wu L; Zhang H; Jin T; Wu J; Sun L J Clin Neurosci; 2014 Jan; 21(1):175-8. PubMed ID: 23787189 [TBL] [Abstract][Full Text] [Related]
5. Genetic cross-interaction between APOE and PRNP in sporadic Alzheimer's and Creutzfeldt-Jakob diseases. Calero O; Bullido MJ; Clarimón J; Frank-García A; Martínez-Martín P; Lleó A; Rey MJ; Rábano A; Blesa R; Gómez-Isla T; Valdivieso F; de Pedro-Cuesta J; Ferrer I; Calero M PLoS One; 2011; 6(7):e22090. PubMed ID: 21799773 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene. Ito Y; Sanjo N; Hizume M; Kobayashi A; Ohgami T; Satoh K; Hamaguchi T; Yamada M; Kitamoto T; Mizusawa H; Yokota T Biochem Biophys Res Commun; 2018 Feb; 496(4):1055-1061. PubMed ID: 29382530 [TBL] [Abstract][Full Text] [Related]
8. [Genetic background of human prion diseases]. Kovács GG Ideggyogy Sz; 2007 Nov; 60(11-12):438-46. PubMed ID: 18198790 [TBL] [Abstract][Full Text] [Related]
9. Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype. Peoc'h K; Manivet P; Beaudry P; Attane F; Besson G; Hannequin D; Delasnerie-Lauprêtre N; Laplanche JL Hum Mutat; 2000 May; 15(5):482. PubMed ID: 10790216 [TBL] [Abstract][Full Text] [Related]
10. Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene. Komatsu J; Sakai K; Hamaguchi T; Sugiyama Y; Iwasa K; Yamada M Prion; 2014; 8(5):336-8. PubMed ID: 25495585 [TBL] [Abstract][Full Text] [Related]
12. Novel mutation of the PRNP gene of a clinical CJD case. Kotta K; Paspaltsis I; Bostantjopoulou S; Latsoudis H; Plaitakis A; Kazis D; Collinge J; Sklaviadis T BMC Infect Dis; 2006 Nov; 6():169. PubMed ID: 17129366 [TBL] [Abstract][Full Text] [Related]
13. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development. Mitrová E; Belay G Acta Virol; 2002; 46(1):31-9. PubMed ID: 12197632 [TBL] [Abstract][Full Text] [Related]
14. A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein. Hainfellner JA; Parchi P; Kitamoto T; Jarius C; Gambetti P; Budka H Ann Neurol; 1999 Jun; 45(6):812-6. PubMed ID: 10360778 [TBL] [Abstract][Full Text] [Related]
15. PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism. Bishop MT; Pennington C; Heath CA; Will RG; Knight RS BMC Med Genet; 2009 Dec; 10():146. PubMed ID: 20035629 [TBL] [Abstract][Full Text] [Related]
16. Report about four novel mutations in the prion protein gene. Schelzke G; Stoeck K; Eigenbrod S; Grasbon-Frodl E; Raddatz LM; Ponto C; Kretzschmar HA; Zerr I Dement Geriatr Cogn Disord; 2013; 35(3-4):229-37. PubMed ID: 23467330 [TBL] [Abstract][Full Text] [Related]
17. Codon 129 polymorphism of the PRNP gene in normal Polish population and in Creutzfeldt-Jakob disease, and the search for new mutations in PRNP gene. Bratosiewicz J; Liberski PP; Kulczycki J; Kordek R Acta Neurobiol Exp (Wars); 2001; 61(3):151-6. PubMed ID: 11584448 [TBL] [Abstract][Full Text] [Related]
18. Rare V203I mutation in the PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease. Shi Q; Chen C; Wang XJ; Zhou W; Wang JC; Zhang BY; Gao C; Gao C; Han J; Dong XP Prion; 2013; 7(3):259-62. PubMed ID: 23764840 [TBL] [Abstract][Full Text] [Related]
19. Novel PRNP mutation in a patient with a slow progressive dementia syndrome. Heinemann U; Krasnianski A; Meissner B; Grasbon-Frodl EM; Kretzschmar HA; Zerr I Med Sci Monit; 2008 May; 14(5):CS41-43. PubMed ID: 18443555 [TBL] [Abstract][Full Text] [Related]
20. A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease. Ripoll L; Laplanche JL; Salzmann M; Jouvet A; Planques B; Dussaucy M; Chatelain J; Beaudry P; Launay JM Neurology; 1993 Oct; 43(10):1934-8. PubMed ID: 8105421 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]