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.
394 related articles for article (PubMed ID: 9629853)
1. Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease. Shibuya S; Higuchi J; Shin RW; Tateishi J; Kitamoto T Ann Neurol; 1998 Jun; 43(6):826-8. PubMed ID: 9629853 [TBL] [Abstract][Full Text] [Related]
2. Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease. Gabizon R; Rosenman H; Meiner Z; Kahana I; Kahana E; Shugart Y; Ott J; Prusiner SB Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):385-90. PubMed ID: 7913755 [TBL] [Abstract][Full Text] [Related]
3. Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease. Croes EA; Alizadeh BZ; Bertoli-Avella AM; Rademaker T; Vergeer-Drop J; Dermaut B; Houwing-Duistermaat JJ; Wientjens DP; Hofman A; Van Broeckhoven C; van Duijn CM Eur J Hum Genet; 2004 May; 12(5):389-94. PubMed ID: 14970845 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease. Erginel-Unaltuna N; Peoc'h K; Komurcu E; Acuner TT; Issever H; Laplanche JL Eur J Hum Genet; 2001 Dec; 9(12):965-8. PubMed ID: 11840201 [TBL] [Abstract][Full Text] [Related]
6. [An autopsy-verified case of Creutzfeldt-Jakob disease with codon 129 polymorphism and codon 180 point mutation]. Matsumura T; Kojima S; Kuroiwa Y; Takagi A; Unakami M; Kitamoto T Rinsho Shinkeigaku; 1995 Mar; 35(3):282-5. PubMed ID: 7614752 [TBL] [Abstract][Full Text] [Related]
7. [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]
8. [Familial Creutzfeldt-Jakob disease with the heterozygous point mutation at codon 200 of the prion protein gene (Glu-->Lys)--report of CJD200 brothers of Yamanashi Prefecture origin]. Kawauchi Y; Okada M; Kuroiwa Y; Ishihara O; Akai J No To Shinkei; 1997 May; 49(5):460-4. PubMed ID: 9163760 [TBL] [Abstract][Full Text] [Related]
9. Genetic epidemiology of Creutzfeldt-Jakob disease in Europe. EUROCJD Group Rev Neurol (Paris); 2001 Jul; 157(6-7):633-7. PubMed ID: 11458182 [TBL] [Abstract][Full Text] [Related]
10. [A case of Creutzfeldt-Jakob disease with a point mutation of prion protein at codon 180]. Tanaka T; Kinoshita I; Saitoh Y; Satoh K; Nishiura Y; Shirabe S; Kitamoto T No To Shinkei; 2004 Dec; 56(12):1025-8. PubMed ID: 15729879 [TBL] [Abstract][Full Text] [Related]
11. Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation. Puoti G; Rossi G; Giaccone G; Awan T; Lievens PM; Defanti CA; Tagliavini F; Bugiani O Ann Neurol; 2000 Aug; 48(2):269-70. PubMed ID: 10939584 [No Abstract] [Full Text] [Related]
12. Polymorphism at codon 129 of the prion protein gene determines cerebellar pathology in Creutzfeldt-Jakob disease. Schulz-Schaeffer WJ; Giese A; Windl O; Kretzschmar HA Clin Neuropathol; 1996; 15(6):353-7. PubMed ID: 8937783 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. [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]
15. [Three patients from two families with familial Creutzfeldt-Jakob disease having a point mutation in the prion protein gene at codon 200 (Glu-->Lys)]. Iwabuchi K; Endoh S; Hagimoto H; Okamoto K; Miyakawa T; Yamaguchi T; Kajiwara A; Inoue K; Yamada Y; Amano N No To Shinkei; 1994 Apr; 46(4):349-54. PubMed ID: 7912945 [TBL] [Abstract][Full Text] [Related]
16. [A case of codon 232 mutation-induced Creutzfeldt-Jakob disease visualized by the MRI-FLAIR images with atypical clinical symptoms]. Saito T; Isozumi K; Komatsumoto S; Nara M; Suzuki K; Dohura K Rinsho Shinkeigaku; 2000 Jan; 40(1):51-4. PubMed ID: 10825802 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Diffusion-weighted MRI in familial Creutzfeldt-Jakob disease with the codon 200 mutation in the prion protein gene. Tsuboi Y; Baba Y; Doh-ura K; Imamura A; Fujioka S; Yamada T J Neurol Sci; 2005 May; 232(1-2):45-9. PubMed ID: 15850581 [TBL] [Abstract][Full Text] [Related]
19. Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population. Jeong BH; Lee KH; Kim NH; Jin JK; Kim JI; Carp RI; Kim YS Neurogenetics; 2005 Dec; 6(4):229-32. PubMed ID: 16217673 [TBL] [Abstract][Full Text] [Related]