Minimal change prion retinopathy: Morphometric comparison of retinal and brain prion deposits in Creutzfeldt-Jakob disease

Authors :: Vanessa S. Goodwill
Ian Dryden
Jihee Choi
Chiara De Lillo
Katrin Soldau
Jorge Llibre-Guerra
Henry Sanchez
Christina J. Sigurdson
Jonathan H. Lin
Source :: Experimental eye research. 222
Publication Year :: 2022
Abstract: Sporadic Creutzfeldt-Jakob disease (sCJD) is the most commonly diagnosed human prion disease caused by the abnormal misfolding of the 'cellular' prion protein (PrP

Subjects :: Cellular and Molecular Neuroscience
Ophthalmology
Retinal Diseases
Prions
Brain
Humans
Gliosis
Sensory Systems
Creutzfeldt-Jakob Syndrome
Retina

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