2017
DOI: 10.20517/2347-8659.2017.01
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Developments in auxiliary examination of Creutzfeldt-Jakob disease

Abstract: How to cite this article: Zhao W, Jiang JJ, Zhang JT. Developments in auxiliary examination of Creutzfeldt-Jakob disease. Neuroimmunol Neuroinflammation 2017;4:136-44.Creutzfeldt-Jakob disease (CJD), which is caused by prion scrapie protein, is a rare, chronic, transmissible and fatal disease. Clinical manifestations of CJD include rapidly progressive dementia, cerebellar ataxia, visual disturbance, as well as pyramidal and extrapyramidal tract signs. Four subtypes of CJD have been reported, including sporadic… Show more

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