Prion diseases
Author:
Publisher
CRC Press
Link
http://www.crcnetbase.com/doi/pdf/10.1201/b13319-17
Reference143 articles.
1. Predicting susceptibility and incubation time of human-to-human transmission of vCJD
2. Prion Protein is Not Detectable in Dental Pulp from Patients with Creutzfeldt-Jakob Disease
3. Clinical course in young patients with sporadic Creutzfeldt-Jakob disease
4. SPONGIFORM ENCEPHALOPATHY TRANSMITTED EXPERIMENTALLY FROM CREUTZFELDT-JAKOB AND FAMILIAL GERSTMANN-STRÄUSSLER-SCHEINKER DISEASES
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1. Sensory disturbances in Creutzfeldt-Jakob disease;Neurological Sciences;2023-10-13
2. Immunohistochemical and ultrastructural evidence for the pathogenesis of white matter degeneration in patients with panencephalopathic‐type Creutzfeldt–Jakob disease: Inducible nitric oxide synthase overexpression in bizarre astrocytes;Neuropathology;2020-04
3. Prion Diseases of Humans;eLS;2015-04-14
4. A case of chronic wasting disease in a captive red deer (Cervus elaphus);Journal of Veterinary Diagnostic Investigation;2013-08-15
5. The application of in vitro cell-free conversion systems to human prion diseases;Acta Neuropathologica;2010-06-10
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