Creutzfeldt-Jakob Disease: Spectrum of Symptoms, Clinical Progress and Diagnostics-Report of Five Cases
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Creutzfeldt-Jakob disease (CJD) is a rare, fatal prion disease of the central nervous system that develops due to the conversion of the normal cellular protein PrPc to the abnormal PrPSc molecule. The first clinical cases were described in the 1920s. The aim o... ...
