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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...

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Bibliografiske detaljer
Principais autores: T. E. Popova, A. A. Tappakhov, T. K. Davydova, T. Ya. Nikolaeva, Yu. I. Khabarova, M. A. Varlamova, L. T. Okoneshinova
Format: Artigo
Sprog:Russo
Udgivet: IMA-PRESS LLC 2020-04-01
Serier:Неврология, нейропсихиатрия, психосоматика
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Online adgang:https://nnp.ima-press.net/nnp/article/view/1310
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