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Carbamazepine Encephalopathy Masquerading as Creutzfeldt-Jakob Disease
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Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
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Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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Clinical Picture in Creutzfeldt-Jakob Disease
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Laboratory Diagnosis of Creutzfeldt-Jakob Disease
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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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Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
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Dressing Apraxia as Initial Manifestation of Creutzfeldt-Jakob Disease
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An Atypical Presentation of Creutzfeldt-Jakob Disease with a Heidenhain Variant and Balints Syndrome
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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RT-QuIC: A New Test for Sporadic CJD
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Cerebellar Ataxia and Hearing Impairment
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Diagnosis of Human Prion Disease Using Real-Time Quaking-Induced Conversion Testing of Olfactory Mucosa and Cerebrospinal Fluid Samples
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Cerebrospinal Fluid Real-Time Quaking-Induced Conversion is a Robust and Reliable Test for Sporadic Creutzfeldt-Jakob Disease: An International Study
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A 64-year-old Man with Visual Distortions
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Rapid and Sensitive RT-QuIC Detection of Human Creutzfeldt-Jakob Disease Using Cerebrospinal Fluid
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A Comparison of Tau and 14-3-3 Protein in the Diagosis of Creutzfeldt-Jakob Disease
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Evidence-based Guideline: Diagnostic accuracy of CSF 14-3-3 Protein in Sporadic Creutzfeldt-Jakob Disease
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Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
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Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias
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Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UK
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Treatable Neurological Disorders Misdiagnosed as Creutzfeldt-Jakob Disease
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Rapidly Progressive Neurodegenerative Dementias
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Transmissible Spongiform Encephalopathy in the 21st Century: Neuroscience for the Clinical Neurologist
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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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MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
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Differential Diagnosis of Restricted Diffusion Confined to the Cerebral Cortex
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Neuroimaging Findings in Human Prion Disease
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Clinicopath conf., Human Prion Disease, Sporadic CJD
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CSF Analysis in Patients With Sporadic CJD and Other Transmissible Spongiform Encephalopathies
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First Symptom in Sporadic Creutzfeldt-Jakob Disease
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CSF Tests in the Differential Diagnosis of Cretuzfeldt-Jakob Disease
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Diffusion-Weighted and Fluid-Attenuated Inversion Recovery Imaging in Creutzfeldt-Jakob Disease:High Sensitivity and Specificity for Diagnosis
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Diffusion-Weighted MRI Abnormalities as an Early Diagnostic Marker for Creutzfeldt-Jakob Disease
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Sensitivity of 14-3-3 Protein Test Varies in Subtypes of Sporadic 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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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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Diagnosing Variant Creutzfeldt-Jakob Disease with the Pulvinar Sign:"MR Imaging Findings in 86 Neuropathologically Confirmed Cases
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Tau Protein and 14-3-3 Protein in the Differential Diagnosis of Creutzfeldt-Jakob Disease
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Conspicuity and Evolution of Lesions in Creutzfeldt-Jakob Disease at Diffusion-Weighted Imaging
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14-3-3 Protein Cerebrspinal Fluid Detection in Human Growth Hormone-Treated Creutzfeldt-Jakob Disease Patients
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CSF Detection of the 14-3-3 Protein in Unselected Patients with Dementia
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Use of 14-3-3 and Other Brain-specific Proteins in CSF in the Diagnosis of Variant Creutzfeldt-Jakob Disease
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