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JNNP 82:646-651, Heath, C.A.,et al, 2011
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JAMA 330:921-922, Greenberg,S.M., 2023
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NEJM 386;674-687, Case 5-2022, 2022
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Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021
Homonymous Hemianopia with Normal Magnetic Resonance Imaging
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020
Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure
NEJM 383:83-85, Brandel, J.P.,et al, 2020
Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019
Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
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Clinicopath conf., Human Prion Disease, Sporadic CJD
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Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
NEJM 353:1042-1050, Case 27-2005, 2005
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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Novel Methods for Disinfection of Prion-Contaminated Medical Devices
Lancet 364:521-526, Fichet,G.,et al, 2004
Preclinical vCJD After Blood Transfusion in a PRNP Codon 129 Heterozygous Patient
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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Transmissible Spongiform Encephalopathies
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
NEJM 324:1091-1097, Hsiao,K.,et al, 1991
The Spongiform Encephalopathies, Editorial
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Prion Dementia Without Characteristic Pathology
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