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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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Treatable Neurological Disorders Misdiagnosed as 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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Challenging the Clinical Utility of the 14-3-3 Protein for the Diagnosis of Sporadic Creutzfeldt-Jakob Disease
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14-3-3 Protein in the CSF of Patients with Rapidly Progressive Dementia
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14-3-3 Testing in Diagnosing Creutzfeldt-Jakob Disease
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Misleading Results With the 14-3-3 Assay for the Diagnosis of Creutzfeldt-Jakob Disease
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The 14-3-3 Brain Protein in Cerebrospinal Fluid as a Marker for Transmissible Spongiform Encephalopathies
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