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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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Homonymous Hemianopia with Normal Magnetic Resonance Imaging
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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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Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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Long-Term Preclinical Magnetic Resonance Imaging Alterations in Sporadic Creutzfeldt-Jakob Disease
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A 64-year-old Man with Visual Distortions
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Treatable Neurological Disorders Misdiagnosed as Creutzfeldt-Jakob Disease
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Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
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Rapidly Progressive Neurodegenerative Dementias
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Sporadic Creutzfeldt-Jakob Disease in Two Adolescents
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Systematic Review of Therapeutic Intervention in Human Prion Disease
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Rapidly Progressive Dementia
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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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Neuroimaging Findings in Human Prion Disease
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Kuru in the 21st Century--An Acquired Human Prion Disease With Very Long Incubation Periods
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Onset of Creutzfeldt-Jakob Disease Mimicking an Acute Cerebrovascular Event
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CSF Tests in the Differential Diagnosis of Cretuzfeldt-Jakob Disease
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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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Transmissible Spongiform Encephalopathies
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Tissue Distribution of Bovine Spongiform Encephalopathy Agent in Primates after Intravenous or Oral Infection
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Possible Transmission of Variant Creutzfeldt-Jakob Disease by Blood Transfusion
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Prion Deposition in Olfactory Biopsy of Sporadic Creutzfeldt-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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Novel Methods for Disinfection of Prion-Contaminated Medical Devices
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Preclinical vCJD After Blood Transfusion in a PRNP Codon 129 Heterozygous Patient
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CJD--A Case of Mistaken Identity
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Antivonvulsants for Creutzfeldt-Jakob Disease?
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Detection of Pathologic Prion Protein in the Olfactory Epithelium 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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Tau Protein and 14-3-3 Protein in the Differential Diagnosis of Creutzfeldt-Jakob Disease
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