Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Diffusion-Weighted MR Imaging of the Brain
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure
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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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Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
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Bilateral Thalamic Lesions
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Transmissible Spongiform Encephalopathy in the 21st Century: Neuroscience for the Clinical Neurologist
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Differential Diagnosis of Restricted Diffusion Confined to the Cerebral Cortex
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Onset of Creutzfeldt-Jakob Disease Mimicking an Acute Cerebrovascular Event
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Carbamazepine Encephalopathy Masquerading as Creutzfeldt-Jakob Disease
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Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
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Surgical Treatment and Risk of Sporadic Creutzfeldt-Jakob Disease:A Case-Control Study
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Mortality from Dementia in Occupations at Risk of Exposure to Bovine Spongiform EncephalopathyAnalysis of Death Registrations
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Case-Control Study of Risk Factors of Creutzfeldt-Jacob Disease in Europe During 1993-95
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The Risk of Bovine Spongiform Encephalopathy ('Mad Cow Disease') to Human Health
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Transmissible Spongiform Encephalopathies
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The 14-3-3 Brain Protein in Cerebrospinal Fluid as a Marker for Transmissible Spongiform Encephalopathies
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Creutzfeldt-Jakob Disease and Bovine Spongiform Encephalopathy:Any Connection?
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Creutzfeldt-Jakob Disease in a Physician:A Review of the Disorder in Health Care Workers
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Creutzfeldt-Jakob Disease in a Pathologist
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Protein Processing in Lysosomes:The New Therapeutic Target in Neurodegenerative Disease
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Demonstration of the Transmissible Agent in Tissue From a Pregnant Woman with Creutzfeldt-Jakob Disease
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Transmission of Alpers'Disease (Chr Prog Encephalopathy) Produces Exper Creutzfeldt-Jakob Disease in Hamsters
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Punctate Diffuse Cortex Signals in Creutzfeldt-Jakob Disease
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Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
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Laboratory Diagnosis of Creutzfeldt-Jakob Disease
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More Than a Little Unsteady
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Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
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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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Long Survival Sporadic Creutzfeldt-Jakob Disease
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A 57-Year-Old Woman with Progressive Ataxia and Falls
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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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Precipitous Deterioration of Motor Function, Cognition, and Behavior
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Distinguishing Neuroimaging Features in Patients Presenting with Visual Hallucinations
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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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Diffusion-Weighted MRI Abnormalities Antedate the Onset of Sporadic 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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Creutzfeldt-Jakob Disease and Hashimotos Thyroiditis: A Case Report Illustrating Prion-Induced Encephalitis
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