A case of sporadic Creutzfeldt-Jakob disease

A case of sporadic Creutzfeldt-Jakob disease

Sporadic Creutzfeldt-Jakob disease (CJD) is a very rare and fatal disease caused by prions – proteins with unique characteristics and infective potential. The typical clinical presentation is of a rapidly progressive dementia with myoclonus, cerebellar, pyramidal, extra pyramidal and visual signs. T...

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Bibliographic Details
Main Authors:	Raoul Pop, Arta Teodorescu, Maria Tanasie, Ruxandra Joikits, Roxana Gheoca, Mihaela Simu
Format:	Article
Language:	English
Published:	Amaltea Medical Publishing House 2012-06-01
Series:	Romanian Journal of Neurology
Subjects:	sporadic creutzfeldt-jakob disease rapidly progressive dementia prion diseases
Online Access:	https://rjn.com.ro/articles/2012.2/RJN_2012_2_Art-05.pdf

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