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13. The evolution of views on the nosological position of transmissible spongiform encephalopathies. Liberski PP, Brown P, Gajdusek CD. Folia Neuropathol; 1997 Dec; 35(4):214-25. PubMed ID: 9833398 [Abstract] [Full Text] [Related]
14. The prion diseases: Creutzfeldt-Jakob, Gerstmann-Sträussler-Scheinker, and related disorders. Mastrianni JA. J Geriatr Psychiatry Neurol; 1998 Dec; 11(2):78-97. PubMed ID: 9877529 [Abstract] [Full Text] [Related]
15. [Gene mutation and pathology in human prion disease]. Tashiro H, Doh-ura K. No To Shinkei; 1997 Aug; 49(8):681-7. PubMed ID: 9282361 [No Abstract] [Full Text] [Related]
18. Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann-Sträussler syndrome. Doh-ura K, Tateishi J, Kitamoto T, Sasaki H, Sakaki Y. Ann Neurol; 1990 Feb; 27(2):121-6. PubMed ID: 2180366 [Abstract] [Full Text] [Related]