| Literature DB >> 14522867 |
S J Tabrizi1, C L Elliott, C Weissmann.
Abstract
Prion diseases or transmissible spongiform encephalopathies are a group of closely related transmissible neurodegenerative conditions of humans and animals, all of which are incurable. In recent years, they have captured public attention with the emergence of the bovine spongiform encephalopathy (BSE) epidemic in Europe, and more recently with the appearance of variant CJD (vCJD) in humans, a novel form of Creutzfeldt-Jakob disease (CJD) that is linked to dietary exposure to BSE. In this chapter, we outline ethical questions posed by research, diagnostic procedures and therapy in the field of prion diseases.Entities:
Keywords: Biomedical and Behavioral Research; Genetics and Reproduction; Health Care and Public Health
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Year: 2003 PMID: 14522867 DOI: 10.1093/bmb/66.1.305
Source DB: PubMed Journal: Br Med Bull ISSN: 0007-1420 Impact factor: 4.291