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Abstract

Creutzfeldt-Jakob Disease (CJD) was first described in 1920-1921. CJD is a rare disease with a reported incidence of 0.5 to 1 case per million people in Europe. This fatal dementia belongs to the category of Transmissible Spongiform Encephalopathies (TSE)

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/content/10.2807/esm.01.06.00158-en
1996-06-01
2017-12-12
http://instance.metastore.ingenta.com/content/10.2807/esm.01.06.00158-en
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