Prion protein accumulation involving the peripheral nervous system in a sporadic case of Creutzfeldt-Jakob disease
- 3 November 2003
- journal article
- research article
- Published by Wiley in Neuropathology and Applied Neurobiology
- Vol. 29 (6) , 602-605
- https://doi.org/10.1046/j.0305-1846.2003.00495.x
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Neurotoxicity and Neurodegeneration When PrP Accumulates in the CytosolScience, 2002
- Laboratory diagnosis of variant Creutzfeldt–Jakob diseaseHistopathology, 2000
- Diagnosis of new variant Creutzfeldt-Jakob diseaseAnnals of Neurology, 2000
- Deposition of disease-associated prion protein involves the peripheral nervous system in experimental scrapieActa Neuropathologica, 1999
- Disease associated prion protein may deposit in the peripheral nervous system in human transmissible spongiform encephalopathiesActa Neuropathologica, 1999
- Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjectsAnnals of Neurology, 1999
- Peripheral neuropathy in Creutzfeldt-Jakob diseaseNeurology, 1997
- Demyelinating peripheral neuropathy with Creutzfeldt-Jakob disease and mutation at codon 200 of the prion protein geneNeurology, 1996
- Prion protein accumulation in the spinal cords of patients with sporadic and growth hormone associated Creutzfeldt-Jakob diseaseNeuroscience Letters, 1995
- Demyelinating peripheral neuropathy in Creutzfeldt–Jakob diseaseMuscle & Nerve, 1992