Literature DB >> 14522867

Ethical issues in human prion diseases.

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


  4 in total

Review 1.  Should desperate volunteers be included in randomised controlled trials?

Authors:  P Allmark; S Mason
Journal:  J Med Ethics       Date:  2006-09       Impact factor: 2.903

2.  Familial Creutzfeldt-Jakob Disease Cluster Among an African American Family.

Authors:  Matthew G Johnson; Kristy K Bradley; Rebecca L Coffman; Ermias D Belay
Journal:  J Public Health Manag Pract       Date:  2017 Nov/Dec

3.  Genetics and genetic counseling: recommendations for Alzheimer's disease, frontotemporal dementia, and Creutzfeldt-Jakob disease.

Authors:  Jennifer Williamson; Susan LaRusse
Journal:  Curr Neurol Neurosci Rep       Date:  2004-09       Impact factor: 5.081

4.  Regulation of prion protein expression: a potential site for therapeutic intervention in the transmissible spongiform encephalopathies.

Authors:  C L Haigh; D R Brown
Journal:  Int J Biomed Sci       Date:  2006-12
  4 in total

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