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6. The diagnosis of human prion diseases. Kordek R. Folia Neuropathol; 2000 Aug 24; 38(4):151-60. PubMed ID: 11693717 [Abstract] [Full Text] [Related]
7. Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. Mead S, Poulter M, Uphill J, Beck J, Whitfield J, Webb TE, Campbell T, Adamson G, Deriziotis P, Tabrizi SJ, Hummerich H, Verzilli C, Alpers MP, Whittaker JC, Collinge J. Lancet Neurol; 2009 Jan 24; 8(1):57-66. PubMed ID: 19081515 [Abstract] [Full Text] [Related]
8. A naturally occurring variant of the human prion protein completely prevents prion disease. Asante EA, Smidak M, Grimshaw A, Houghton R, Tomlinson A, Jeelani A, Jakubcova T, Hamdan S, Richard-Londt A, Linehan JM, Brandner S, Alpers M, Whitfield J, Mead S, Wadsworth JD, Collinge J. Nature; 2015 Jun 25; 522(7557):478-81. PubMed ID: 26061765 [Abstract] [Full Text] [Related]
9. Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. Mead S, Uphill J, Beck J, Poulter M, Campbell T, Lowe J, Adamson G, Hummerich H, Klopp N, Rückert IM, Wichmann HE, Azazi D, Plagnol V, Pako WH, Whitfield J, Alpers MP, Whittaker J, Balding DJ, Zerr I, Kretzschmar H, Collinge J. Hum Mol Genet; 2012 Apr 15; 21(8):1897-906. PubMed ID: 22210626 [Abstract] [Full Text] [Related]
10. Human prion diseases: from Kuru to variant Creutzfeldt-Jakob disease. Sikorska B, Liberski PP. Subcell Biochem; 2012 Apr 15; 65():457-96. PubMed ID: 23225013 [Abstract] [Full Text] [Related]
11. The French surveillance network of Creutzfeldt-Jakob disease. Epidemiological data in France and worldwide. Brandel JP, Peckeu L, Haïk S. Transfus Clin Biol; 2013 Sep 15; 20(4):395-7. PubMed ID: 23587616 [Abstract] [Full Text] [Related]
13. Kuru and "new variant" CJD. Verdrager J. Southeast Asian J Trop Med Public Health; 1997 Sep 15; 28(3):535-40. PubMed ID: 9561604 [Abstract] [Full Text] [Related]
14. Creutzfeldt-Jakob disease and related transmissible spongiform encephalopathies. Johnson RT, Gibbs CJ. N Engl J Med; 1998 Dec 31; 339(27):1994-2004. PubMed ID: 9869672 [No Abstract] [Full Text] [Related]
15. [Epidemiology of human prion diseases]. Kondo K. Nihon Rinsho; 1997 Apr 31; 55(4):978-86. PubMed ID: 9103905 [Abstract] [Full Text] [Related]
16. Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1. Mead S, Mahal SP, Beck J, Campbell T, Farrall M, Fisher E, Collinge J. Am J Hum Genet; 2001 Dec 31; 69(6):1225-35. PubMed ID: 11704923 [Abstract] [Full Text] [Related]
17. The many faces of human prion diseases in Belgium and the world. Van Everbroeck B, Pals P, Quoilin S, Martin JJ, Cras P. Acta Neurol Belg; 2001 Jun 31; 101(2):81-7. PubMed ID: 11486562 [Abstract] [Full Text] [Related]
18. [Comments on present-day spread and epidemiology of BSE and prion diseases]. Bodemer W, Kaup FJ. Gesundheitswesen; 2004 Feb 31; 66 Suppl 1():S21-5. PubMed ID: 14770333 [Abstract] [Full Text] [Related]
19. Prions, mad cow disease, and preventive measures: a critical appraisal. Bhakdi S, Bohl J. Med Microbiol Immunol; 2003 Aug 31; 192(3):117-22. PubMed ID: 12819966 [No Abstract] [Full Text] [Related]
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