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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. Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study. Jones E; Hummerich H; Viré E; Uphill J; Dimitriadis A; Speedy H; Campbell T; Norsworthy P; Quinn L; Whitfield J; Linehan J; Jaunmuktane Z; Brandner S; Jat P; Nihat A; How Mok T; Ahmed P; Collins S; Stehmann C; Sarros S; Kovacs GG; Geschwind MD; Golubjatnikov A; Frontzek K; Budka H; Aguzzi A; Karamujić-Čomić H; van der Lee SJ; Ibrahim-Verbaas CA; van Duijn CM; Sikorska B; Golanska E; Liberski PP; Calero M; Calero O; Sanchez-Juan P; Salas A; Martinón-Torres F; Bouaziz-Amar E; Haïk S; Laplanche JL; Brandel JP; Amouyel P; Lambert JC; Parchi P; Bartoletti-Stella A; Capellari S; Poleggi A; Ladogana A; Pocchiari M; Aneli S; Matullo G; Knight R; Zafar S; Zerr I; Booth S; Coulthart MB; Jansen GH; Glisic K; Blevins J; Gambetti P; Safar J; Appleby B; Collinge J; Mead S Lancet Neurol; 2020 Oct; 19(10):840-848. PubMed ID: 32949544 [TBL] [Abstract][Full Text] [Related]
5. No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease. Sánchez-Juan P; Bishop MT; Green A; Giannattasio C; Arias-Vasquez A; Poleggi A; Knight RS; van Duijn CM BMC Med Genet; 2007 Dec; 8():77. PubMed ID: 18072964 [TBL] [Abstract][Full Text] [Related]
6. A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk. Sanchez-Juan P; Bishop MT; Kovacs GG; Calero M; Aulchenko YS; Ladogana A; Boyd A; Lewis V; Ponto C; Calero O; Poleggi A; Carracedo Á; van der Lee SJ; Ströbel T; Rivadeneira F; Hofman A; Haïk S; Combarros O; Berciano J; Uitterlinden AG; Collins SJ; Budka H; Brandel JP; Laplanche JL; Pocchiari M; Zerr I; Knight RS; Will RG; van Duijn CM PLoS One; 2014; 10(4):e0123654. PubMed ID: 25918841 [TBL] [Abstract][Full Text] [Related]
7. Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study. Balendra R; Uphill J; Collinson C; Druyeh R; Adamson G; Hummerich H; Zerr I; Gambetti P; Collinge J; Mead S BMC Med Genet; 2016 Apr; 17():28. PubMed ID: 27055460 [TBL] [Abstract][Full Text] [Related]
8. PRNP contains both intronic and upstream regulatory regions that may influence susceptibility to Creutzfeldt-Jakob Disease. McCormack JE; Baybutt HN; Everington D; Will RG; Ironside JW; Manson JC Gene; 2002 Apr; 288(1-2):139-46. PubMed ID: 12034503 [TBL] [Abstract][Full Text] [Related]
9. Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008. Begué C; Martinetto H; Schultz M; Rojas E; Romero C; D'Giano C; Sevlever G; Somoza M; Taratuto AL Neuroepidemiology; 2011; 37(3-4):193-202. PubMed ID: 22067221 [TBL] [Abstract][Full Text] [Related]
10. Dealing with the uncertain risk of variant Creutzfeldt-Jakob disease transmission by coagulation replacement products. Millar CM; Makris M Br J Haematol; 2012 Aug; 158(4):442-52. PubMed ID: 22775486 [TBL] [Abstract][Full Text] [Related]
11. [Creutzfeldt-Jakob disease--the past or the future]. Kulczycki J Przegl Epidemiol; 2006; 60 Suppl 1():63-7. PubMed ID: 16909780 [TBL] [Abstract][Full Text] [Related]
12. Apolipoprotein E and other cerebrospinal fluid proteins differentiate ante mortem variant Creutzfeldt-Jakob disease from ante mortem sporadic Creutzfeldt-Jakob disease. Choe LH; Green A; Knight RS; Thompson EJ; Lee KH Electrophoresis; 2002 Jul; 23(14):2242-6. PubMed ID: 12210228 [TBL] [Abstract][Full Text] [Related]
13. MHC typing in variant Creutzfeldt-Jakob disease. Pepys MB; Bybee A; Booth DR; Bishop MT; Will RG; Little AM; Prokupek B; Madrigal JA Lancet; 2003 Feb; 361(9356):487-9. PubMed ID: 12583949 [TBL] [Abstract][Full Text] [Related]
14. Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada. Ladogana A; Puopolo M; Croes EA; Budka H; Jarius C; Collins S; Klug GM; Sutcliffe T; Giulivi A; Alperovitch A; Delasnerie-Laupretre N; Brandel JP; Poser S; Kretzschmar H; Rietveld I; Mitrova E; Cuesta Jde P; Martinez-Martin P; Glatzel M; Aguzzi A; Knight R; Ward H; Pocchiari M; van Duijn CM; Will RG; Zerr I Neurology; 2005 May; 64(9):1586-91. PubMed ID: 15883321 [TBL] [Abstract][Full Text] [Related]
15. Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profiles. Lewis V; Hill AF; Klug GM; Boyd A; Masters CL; Collins SJ Neurology; 2005 Jul; 65(1):113-8. PubMed ID: 16009895 [TBL] [Abstract][Full Text] [Related]
16. Young-onset CJD: age and disease phenotype in variant and sporadic forms. Corato M; Cereda C; Cova E; Ferrarese C; Ceroni M Funct Neurol; 2006; 21(4):211-5. PubMed ID: 17367581 [TBL] [Abstract][Full Text] [Related]
17. Genetic risk factors associated with Creutzfeld-Jakob disease in Slovenians and a rapid typing for PRNP codon 129 single nucleotide polymorphism. Galvani V; Rupreht RR; Serbec VC; Vidan-Jeras B Transfus Med; 2005 Jun; 15(3):197-207. PubMed ID: 15943704 [TBL] [Abstract][Full Text] [Related]
18. Cerebrospinal fluid biomarkers in Creutzfeldt-Jakob disease. Van Everbroeck B; Boons J; Cras P Clin Neurol Neurosurg; 2005 Aug; 107(5):355-60. PubMed ID: 16023527 [TBL] [Abstract][Full Text] [Related]
19. [Psychiatric manifestations of a new variant of Creutzfeldt-Jakob disease. Apropos of a case]. Dervaux A; Vicart S; Lopes F; Le Borgne MH Encephale; 2001; 27(2):194-7. PubMed ID: 11407273 [TBL] [Abstract][Full Text] [Related]
20. Description and analysis of 12 years of surveillance for Creutzfeldt-Jakob disease in Denmark, 1997 to 2008. Gubbels S; Bacci S; Laursen H; Hogenhaven H; Cowan S; Molbak K; Christiansen M Euro Surveill; 2012 Apr; 17(15):. PubMed ID: 22516048 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]