Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease
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Title
Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease
Authors
Keywords
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Journal
NEUROPATHOLOGY
Volume 35, Issue 4, Pages 336-342
Publisher
Wiley
Online
2015-03-18
DOI
10.1111/neup.12192
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- Incipient intranuclear inclusion body disease in a 78-year-old woman
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- Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients
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- (2008) I. Ferrer et al. BRAIN
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