Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
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Rapid Progression of Prion Disease Associated with Transverse Myelitis
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Dressing Apraxia as Initial Manifestation of Creutzfeldt-Jakob Disease
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
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Evidence-based Guideline: Diagnostic accuracy of CSF 14-3-3 Protein in Sporadic Creutzfeldt-Jakob Disease
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Isolated Cortical Signal Increase on MR Imaging as a Frequent Lesion Pattern in Sporadic Creutzfeldt-Jakob Disease
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Clinicopath conf., Human Prion Disease, Sporadic CJD
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14-3-3 Protein in the CSF of Patients with Rapidly Progressive Dementia
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CSF Detection of the 14-3-3 Protein in Unselected Patients with Dementia
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Dementia with Lewy Bodies in a Neuropathologic Series of Suspected Creutzfeldt-Jakob Disease
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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The 14-3-3 Brain Protein in Cerebrospinal Fluid as a Marker for Transmissible Spongiform Encephalopathies
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