A correlative study of the clinical, pathological and biochemical features of sporadic Creutzfeldt-Jakob Disease, 2000-2006
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sporadic CJD (sCJD) is the most common form of human transmissible spongiform encephalopathy (TSE) and is characterised by accumulation of pathological prion protein (PrP) in the central nervous tissue....
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University of Leicester
2013
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.593698 |