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Oxford University Press

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Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease

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Atypical sporadic CJD‐MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease

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John Wiley & Sons Inc

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Sporadic Creutzfeldt–Jakob disease without dementia at onset: clinical features, laboratory tests and sequential diffusion MRI (in an autopsy–proven case)

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