Objective: We aimed to characterize the epidemiological and clinical characteristics of
sporadic Creutzfeldt–Jakob disease (sCJD) in eastern China in this retrospective study …

Case 31, resulting in death in 2014, was discussed at the previous meeting, but the
neuropathological confirmation we have now was not yet available. This case increases the …

Prion disorders are a category of neurodegenerative illnesses caused by prions, which are
misfolded proteins. Prions serve as a folding template for proteins during post-translational …

An accurate diagnosis gives leeway to cost-effective treatments. However, many diseases
continue to evolve; hence, their etiology is sometimes missed due to the procedures used …

Human prion diseases are characterized by rapid fatal neurodegeneration caused by
pathologic prion proteins that are transmissible under specific circumstances. Although the …

Abstract Prion Diseases and Feline Spongiform Encephalopathy• First Described: Feline
spongiform encephalopathy was first recognized in 1990, but prion diseases of sheep and …