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Homonymous Hemianopia with Normal Magnetic Resonance Imaging
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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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Cerebellar Ataxia and Hearing Impairment
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Rapid and Sensitive RT-QuIC Detection of Human Creutzfeldt-Jakob Disease Using Cerebrospinal Fluid
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Treatable Neurological Disorders Misdiagnosed as Creutzfeldt-Jakob Disease
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Pathologic Correlates of Diffusion MRI Changes in Creutzfeldt-Jakob Disease
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MRI Lesion Profiles in Sporadic Creutzfeldt-Jakob Disease
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Rapidly Progressive Dementia
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Voltage-Gated Potassium Channel Autoimmunity Mimicking Creutzfeldt-Jakob Disease
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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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Challenging the Clinical Utility of the 14-3-3 Protein for the Diagnosis of Sporadic Creutzfeldt-Jakob Disease
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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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Extraneural Pathologic Prion Protein in Sporadic Creutzfeldt-Jakob Disease
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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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The Pulvinar Sign on Magnetic Resonance Imaging in Variant Creutzfeldt-Jakob Disease
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Diagnosis of New Variant Creutzfeldt-Jakob Disease
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