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The Risk of Bovine Spongiform Encephalopathy ('Mad Cow Disease') to Human Health
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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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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Long-Term Preclinical Magnetic Resonance Imaging Alterations in Sporadic Creutzfeldt-Jakob Disease
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Early Clinical Signs and Imaging Findings in Gerstmann-Straussler-Scheinker Syndrome (Pro102Leu)
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Prion Deposition in Olfactory Biopsy of 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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Diffusion-Weighted Imaging Discriminates Progressive Supranuclear Palsy from PD, But Not From the Parkinson Variant of Multiple System Atrophy
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Investigation of Variant Creutzfeldt-Jakob Disease and Other Human Prion Diseases with Tonsil Biopsy Samples
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New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
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Systematic Review of Therapeutic Intervention in Human Prion Disease
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Transmissible Spongiform Encephalopathy in the 21st Century: Neuroscience for the Clinical Neurologist
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Possible Transmission of Variant Creutzfeldt-Jakob Disease by Blood Transfusion
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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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Neurodegenerative Diseases and Prions
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Transmissible Spongiform Encephalopathies
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Human Spongiform Encephalopathy:The NIH Series of 300 Cases of Experimentally Transmitted Disease
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Infectious Prions or Cytotoxic Metabolites?
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The Spongiform Encephalopathies, Editorial
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Prions & Neurodegenerative Diseases
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