Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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Clinicopathologic Conference, Genetic 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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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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Dressing Apraxia as Initial Manifestation of Creutzfeldt-Jakob Disease
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Long-Term Preclinical Magnetic Resonance Imaging Alterations in Sporadic Creutzfeldt-Jakob Disease
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
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Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
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Rapidly Progressive Dementia
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Clinicopath conf., Human Prion Disease, Sporadic CJD
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Early Clinical Signs and Imaging Findings in Gerstmann-Straussler-Scheinker Syndrome (Pro102Leu)
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Clinicopath Conf, Prion Disease (Sporadic 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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14-3-3 Testing in Diagnosing Creutzfeldt-Jakob Disease
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Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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Creutzfeldt-Jakob Disease in a Young Woman
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The 14-3-3 Brain Protein in Cerebrospinal Fluid as a Marker for Transmissible Spongiform Encephalopathies
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Diagnosis of Creutzfeldt-Jakob Disease in Two-Dimensional Gel Electrophoresis of Cerebrospinal Fluid
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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