Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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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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The 14-3-3 Brain Protein in Cerebrospinal Fluid as a Marker for Transmissible Spongiform Encephalopathies
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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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Clinicopath conf., Human Prion Disease, Sporadic CJD
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CSF Detection of the 14-3-3 Protein in Unselected Patients with Dementia
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Laboratory Diagnosis of Creutzfeldt-Jakob Disease
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A 64-year-old Man with Visual Distortions
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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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Carbamazepine Encephalopathy Masquerading as Creutzfeldt-Jakob Disease
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CJD--A Case of Mistaken Identity
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Antivonvulsants for Creutzfeldt-Jakob Disease?
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14-3-3 Protein in the CSF of Patients with Rapidly Progressive Dementia
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Quantitation of 14-3-3 and Neurol-Specific Enolase Proteins in CSF in Creutzfeldt-Jakob Disease
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14-3-3 Protein in the CSF as Prognostic Marker in Early Multiple Sclerosis
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14-3-3 Testing in Diagnosing Creutzfeldt-Jakob Disease
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Dementia with Lewy Bodies in a Neuropathologic Series of Suspected Creutzfeldt-Jakob Disease
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