Creutzfeldt–Jakob disease in the Republic of Sakha (Yakutia)

Creutzfeldt–Jakob disease (CJD) is a rare neurodegenerative disease caused by the accumulation of the pathological isoform of prion protein. The classic clinical presentation of CJD is characterized by rapidly progressive dementia, ataxia, myoclonus, and akinetic mutism at the terminal stage of the...

Full description

Bibliographic Details
Main Authors: T. E. Popova, A. A. Tappakhov, T. K. Davydova, T. Ya. Nikolaeva, Yu. I. Khabarova, M. A. Varlamova, L. T. Okoneshinova
Format: Article
Language:Russian
Published: IMA-PRESS LLC 2020-04-01
Series:Неврология, нейропсихиатрия, психосоматика
Subjects:
Online Access:https://nnp.ima-press.net/nnp/article/view/1310