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Creutzfeldt-Jakob disease and vision
Richard A. Armstrong
Optometry
Ophthalmic Research Group
College of Health and Life Sciences
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peer-review
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Keyphrases
Creutzfeldt-Jakob Disease
100%
Visual Symptoms
50%
Cornea
50%
Transmissible Spongiform Encephalopathy
50%
Lymphoid Tissue
50%
Plaque Growth
25%
Brain Tissue
25%
Disease Duration
25%
Immune Response
25%
Prion Protein
25%
Visual Disturbance
25%
Spleen
25%
Sporadic CJD
25%
Florid Plaque
25%
Optical Devices
25%
Classical Form
25%
Supranuclear Palsy
25%
Corneal Dendritic Cells
25%
Hallucinations
25%
Saccadic Pursuit
25%
Disease Course
25%
Tonsil
25%
Disease Presentation
25%
Diplopia
25%
Anterior Eye Segment
25%
Smooth Pursuit Movement
25%
Cortical Blindness
25%
Homonymous Visual Field Defects
25%
Early Age of Onset
25%
Psychiatric Presentation
25%
Medicine and Dentistry
Disease
100%
Creutzfeldt-Jakob Disease
100%
Transmissible Spongiform Encephalopathy
33%
Lymphatic Tissue
33%
Immune Response
16%
Vision Disorder
16%
Prion Protein
16%
Variant Creutzfeldt-Jakob Disease
16%
Onset Age
16%
Dendritic Cell
16%
Movement Perception
16%
Visual Field Defect
16%
Brain Tissue
16%
Cerebral Blindness
16%
Supranuclear Palsy
16%
Hallucination
16%
Diplopia
16%
Tonsil
16%
Neuroscience
Creutzfeldt Jakob Disease
100%
Transmissible Spongiform Encephalopathy
50%
Lymphatic Tissue
50%
Cornea
50%
Visual Field Defect
25%
Prion Protein
25%
Hallucination
25%
Variant Creutzfeldt Jakob Disease
25%
Cortical Blindness
25%
Smooth Pursuit
25%
Diplopia
25%
Supranuclear Palsy
25%
Optical Devices
25%
Tonsil
25%