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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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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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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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Treatable Neurological Disorders Misdiagnosed as Creutzfeldt-Jakob Disease
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Rapidly Progressive Neurodegenerative Dementias
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Clinicopath conf., Human Prion Disease, Sporadic CJD
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CSF Tests in the Differential Diagnosis of Cretuzfeldt-Jakob Disease
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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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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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Tau Protein and 14-3-3 Protein in the Differential Diagnosis of Creutzfeldt-Jakob Disease
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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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Diagnosis of New Variant Creutzfeldt-Jakob Disease
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14-3-3 Testing in Diagnosing Creutzfeldt-Jakob Disease
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Current Clinical Diagnosis in Creutzfeldt-Jakob Disease; Identification of Uncommon Variants
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Analysis of EEG and CSF 14-3-3 proteins as adis to the diagnosis of 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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Dementia with Lewy Bodies in a Neuropathologic Series of Suspected Creutzfeldt-Jakob Disease
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Detection of 14-3-3 Protein in Cerebrospinal Fluid Supports Dx of Creutzfeldt-Jakob Disease
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Detection of 14-3-3 Protein in the CSF of Genetic Creutzfeldt-Jakob Disease
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Bovine Spongiform Encephalopathy and Creutzfeldt-Jakob Disease
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