Diagnosis and Incidence of Prion (Creutzfeldt-Jakob) Disease: A Retrospective Archival Survey with Implications for Future Research

Reliable identification of Creutzfeldt-Jakob disease (CJD) in the UX has become essential following the suggestion that prion disease in cattle (BSE) might transmit, accidentally, to humans who eat contaminated beef. Recent data suggest that some cases of CJD may be clinically unrecognized; in order...

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Veröffentlicht in:	Neurodegeneration (London, England) England), 1995-12, Vol.4 (4), p.357-368
Hauptverfasser:	Bruton, C.J., Bruton, R.K., Gentleman, S.M., Roberts, G.W.
Format:	Artikel
Sprache:	eng
Schlagworte:	Aged Creutzfeldt-Jakob Disease Creutzfeldt-Jakob Syndrome - epidemiology Creutzfeldt-Jakob Syndrome - pathology Creutzfeldt-Jakob Syndrome - transmission diagnosis Female Forecasting human spongiform encephalopathy Humans Immunohistochemistry Male Middle Aged neuropathology prion protein Retrospective Studies
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