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BSE and human prion disease

Published online by Cambridge University Press:  03 January 2018

Paul J. Harrison*
Affiliation:
University Department of Psychiatry, Warneford Hospital, Oxford 0X3 7JX
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Abstract

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Type
Editorials
Copyright
Copyright © 1997 The Royal College of Psychiatrists 

References

Almond, J. W., Brown, P., Gore, S. M., et al (1995) Creutzfeldt-Jakob disease and bovine spongiform encephalopathy: any connection? British Medical Journal, 311, 14151421.CrossRefGoogle ScholarPubMed
Anderson, R. M., Donelly, C. A., Ferguson, N. M., et al (1996) Transmission dynamics and epidemiology of BSE in British cattle. Nature, 382, 779788.CrossRefGoogle ScholarPubMed
Anonymous (1998) Less beef, more brain. Lancet, 347, 915.Google Scholar
Anonymous (1998) Trumping science in BSE. Lancet. 348, 835.Google Scholar
Anonymous (1998) Betraying the public over nvCJD risk. Lancet, 348, 1529.Google Scholar
Baker, H. F. & Ridley, R. M. (1996) What went wrong in BSE? From prion disease to public disaster. Brain Research Bulletin, 40, 237244.CrossRefGoogle ScholarPubMed
Brown, P. (1996) Bovine spongiform encephalopathy and Creutzfeldt-Jakob disease. British Medical Journal, 312, 790791.CrossRefGoogle ScholarPubMed
Collee, J. G. (1996) A dreadful challenge. Lancet. 347, 917918.CrossRefGoogle ScholarPubMed
Collinge, J. (1996) New diagnostic tests for prion diseases. New England Journal of Medicine, 335, 963965.CrossRefGoogle ScholarPubMed
Collinge, J., Sidle, K. C. L., Meads, J., et al (1996) Molecular analysis of prion strain variation and the aetiology of new variant’ CJD. Nature. 383, 685690.CrossRefGoogle ScholarPubMed
Cousens, S. N., Vynnycyk, E., Zeidler, M., et al (1997) Predicting the CJD epidemic in humans. Nature, 385, 197198.CrossRefGoogle ScholarPubMed
Dealler, S. F. (1996) UK adults' risk from eating beef. Lancet, 347, 195196.CrossRefGoogle ScholarPubMed
Fleminger, S. & Curtis, D. (1997) Prion disease. British Journal of Psychiatry, 170, 103105.CrossRefGoogle Scholar
Gibbs, C. J. Jr, Amyx, H. L., Bacote, A., et al (1980) Oral transmission of kuru. Creutzfeldt-Jakob disease and scrapie to non-human primates. Journal of Infectious Diseases, 142, 205208.CrossRefGoogle Scholar
Gore, S. M. (1996) Bovine Creutzfeldt-Jakob disease? British Medical Journal, 312, 791792.CrossRefGoogle ScholarPubMed
Harrison, P. J. & Roberts, G. W. (1992) How now mad cow? British Medical Journal, 304, 929930.CrossRefGoogle ScholarPubMed
Hill, A. F., Zeidler, M., Ironside, J., et al (1997) Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy. Lancet, 349, 99100.CrossRefGoogle ScholarPubMed
Hsich, G., Kenney, K., Gibbs, C. J., et al (1996) The 14-3-3 protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. New England Journal of Medicine, 335, 924930.CrossRefGoogle ScholarPubMed
Lasmézas, C. I., Deslys, J.-P., Demaimay, R., et al (1996) BSE transmission to macaques. Nature, 381, 743744.CrossRefGoogle ScholarPubMed
Lee, K. H. & Harrington, M. G. (1996) Premortem diagnosis of Creutzfeldt-Jakob disease by cerebrospinal fluid analysis. Lancet, 348, 887.CrossRefGoogle ScholarPubMed
Maddocks, A. & Deader, S. (1996) Trumping science in BSE. Lancet, 348, 1520.CrossRefGoogle ScholarPubMed
McKee, M., Lang, T. & Roberts, J. A. (1996) Deregulating health: policy lessons from the BSE affair. Journal of the Royal Society of Medicine, 89, 424426.CrossRefGoogle ScholarPubMed
Parchi, P., Castellani, R., Capellari, S., et al (1996) Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Annals of Neurology, 39, 767778.CrossRefGoogle ScholarPubMed
Prusiner, S. B. (1993) Genetic and infectious prion diseases. Archives of Neurology, 50, 11291153.CrossRefGoogle ScholarPubMed
Sakaguchi, S., Katamine, S., Nishida, N., et al (1996) Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene. Nature, 380, 528531.CrossRefGoogle ScholarPubMed
Schreuder, B. E. C., Van Keulen, L J. M., Vromans, M. E. W., et al (1996) Preclinical test for prion diseases. Nature. 381, 563.CrossRefGoogle ScholarPubMed
Tobler, I., Gaus, S. E., Deboer, T., et al (1996) Altered circadian rhythms and sleep in mice devoid of prion protein. Nature. 380, 639642.CrossRefGoogle ScholarPubMed
Wientjens, D. P. W. M., Davanipour, Z., Hoffman, A., et al (1996) Risk factors from Creutzfeldt-Jakob disease: A reanalysis of case-control studies. Neurology, 48, 12871291.CrossRefGoogle Scholar
Wilesmith, J. W., Ruan, J. B. M. & Atkinson, M. J. (1991) Bovine spongiform encephalopathy: epidemiological studies on the origin. Veterinary Record, 128, 199203.CrossRefGoogle ScholarPubMed
Will, R. G., Ironside, J. W., Zeidler, M., et al (1998) A new variant of Creutzfeldt-Jakob disease in the UK. Lancet, 347, 921925.CrossRefGoogle Scholar
Will, R. G., Ironside, J. W., Zeidler, M., Zeidler, M., Brown, R., et al (1998) Cerebrospinal fluid test for new-variant Creutzfeldt-Jakob disease. Lancet, 348, 955.CrossRefGoogle Scholar
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