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.
115 related articles for article (PubMed ID: 11240560)
21. Mutation at codon 210 (V210I) of the prion protein gene in a North African patient with Creutzfeldt-Jakob disease. Mouillet-Richard S; Teil C; Lenne M; Hugon S; Taleb O; Laplanche JL J Neurol Sci; 1999 Oct; 168(2):141-4. PubMed ID: 10526198 [TBL] [Abstract][Full Text] [Related]
22. The M129V polymorphism of codon 129 in the prion gene (PRNP) in the Danish population. Dyrbye H; Broholm H; Dziegiel MH; Laursen H Eur J Epidemiol; 2008; 23(1):23-7. PubMed ID: 17987393 [TBL] [Abstract][Full Text] [Related]
23. [Clinicopathological characteristics of Creutzfeldt-Jakob disease with a PrP V180I mutation and M129V polymorphism on different alleles]. Iwaski Y; Sone M; Kato T; Yoshida E; Indo T; Yoshida M; Hashizume Y; Yamada M Rinsho Shinkeigaku; 1999 Aug; 39(8):800-6. PubMed ID: 10586622 [TBL] [Abstract][Full Text] [Related]
24. Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases. Kim MO; Cali I; Oehler A; Fong JC; Wong K; See T; Katz JS; Gambetti P; Bettcher BM; Dearmond SJ; Geschwind MD Acta Neuropathol Commun; 2013 Dec; 1():80. PubMed ID: 24330864 [TBL] [Abstract][Full Text] [Related]
25. Allelic variations in apolipoprotein E and prion protein genotype related to plaque formation and age of onset in sporadic Creutzfeldt-Jakob disease. Pickering-Brown SM; Mann DM; Owen F; Ironside JW; de Silva R; Roberts DA; Balderson DJ; Cooper PN Neurosci Lett; 1995 Mar; 187(2):127-9. PubMed ID: 7783958 [TBL] [Abstract][Full Text] [Related]
26. Serial magnetic resonance imaging changes in sporadic Creutzfeldt-Jakob disease with valine homozygosity at codon 129 of the prion protein gene. Furukawa F; Ishibashi S; Sanjo N; Yamashita H; Mizusawa H JAMA Neurol; 2014 Sep; 71(9):1186-7. PubMed ID: 25070174 [No Abstract] [Full Text] [Related]
27. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism. Goldfarb LG; Petersen RB; Tabaton M; Brown P; LeBlanc AC; Montagna P; Cortelli P; Julien J; Vital C; Pendelbury WW Science; 1992 Oct; 258(5083):806-8. PubMed ID: 1439789 [TBL] [Abstract][Full Text] [Related]
28. Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studies. Haltia M; Kovanen J; Goldfarb LG; Brown P; Gajdusek DC Eur J Epidemiol; 1991 Sep; 7(5):494-500. PubMed ID: 1684756 [TBL] [Abstract][Full Text] [Related]
29. Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease. Hsiao K; Meiner Z; Kahana E; Cass C; Kahana I; Avrahami D; Scarlato G; Abramsky O; Prusiner SB; Gabizon R N Engl J Med; 1991 Apr; 324(16):1091-7. PubMed ID: 2008182 [TBL] [Abstract][Full Text] [Related]
30. [Creutzfeldt-Jakob disease with a point mutation at codon 232 of prion protein--a case report]. Shimizu T; Tanaka K; Tanahashi N; Fukuuchi Y; Kitamoto T Rinsho Shinkeigaku; 1994 Jun; 34(6):590-2. PubMed ID: 7955719 [TBL] [Abstract][Full Text] [Related]
31. Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes. Diack AB; Boyle A; Plinston C; Hunt E; Bishop MT; Will RG; Manson JC Brain; 2019 May; 142(5):1416-1428. PubMed ID: 30938429 [TBL] [Abstract][Full Text] [Related]
32. Neuropathological phenotype and 'prion protein' genotype correlation in sporadic Creutzfeldt-Jakob disease. de Silva R; Ironside JW; McCardle L; Esmonde T; Bell J; Will R; Windl O; Dempster M; Estibeiro P; Lathe R Neurosci Lett; 1994 Sep; 179(1-2):50-2. PubMed ID: 7845623 [TBL] [Abstract][Full Text] [Related]
33. Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome. Kitamoto T; Ohta M; Doh-ura K; Hitoshi S; Terao Y; Tateishi J Biochem Biophys Res Commun; 1993 Mar; 191(2):709-14. PubMed ID: 8461023 [TBL] [Abstract][Full Text] [Related]
34. Slow-progressive ataxia with a methionine-to-arginine point mutation in codon 232 in the prion protein gene (PRNP). Nishimoto Y; Ito D; Suzuki S; Shimizu T; Kitamoto T; Suzuki N Clin Neurol Neurosurg; 2011 Oct; 113(8):696-8. PubMed ID: 21620563 [No Abstract] [Full Text] [Related]
35. A Chinese Creutzfeldt-Jakob disease patient with E196K mutation in PRNP. Shi Q; Chen C; Song XN; Gao C; Tian C; Zhou W; Song XH; Yao LS; Han J; Dong XP Prion; 2011; 5(2):117-20. PubMed ID: 21597335 [TBL] [Abstract][Full Text] [Related]
36. 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]
37. A Japanese case of Creutzfeldt-Jakob disease with a point mutation in the prion protein gene at codon 210. Furukawa H; Kitamoto T; Hashiguchi H; Tateishi J J Neurol Sci; 1996 Sep; 141(1-2):120-2. PubMed ID: 8880705 [TBL] [Abstract][Full Text] [Related]
38. Prion mutation D178N with highly variable disease onset and phenotype. Synofzik M; Bauer P; Schöls L J Neurol Neurosurg Psychiatry; 2009 Mar; 80(3):345-6. PubMed ID: 19228673 [TBL] [Abstract][Full Text] [Related]
39. Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene. Hauw JJ; Sazdovitch V; Laplanche JL; Peoc'h K; Kopp N; Kemeny J; Privat N; Delasnerie-Lauprêtre N; Brandel JP; Deslys JP; Dormont D; Alpérovitch A Neurology; 2000 Apr; 54(8):1641-6. PubMed ID: 10762506 [TBL] [Abstract][Full Text] [Related]
40. Familial Creutzfeldt-Jakob disease with a mutation at codon 180 presenting with an atypical phenotype. Yeo MJ; Lee SH; Lee SY; Jeon YC; Park SJ; Cho HJ; Choi KC; Kim YS; Kim SH J Clin Neurosci; 2013 Jan; 20(1):180-2. PubMed ID: 22999564 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]