Author: "Capellari S" / Database: Gale General OneFile - Searchworks@Jio Institute Digital Library Search Results

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Author: Jansen, C., van Swieten, J.C., Capellari, S., Strammiello, R., Parchi, P., and Rozemuller, A.J.M.
Subjects: Creutzfeldt-Jakob disease -- Genetic aspects, Creutzfeldt-Jakob disease -- Case studies, Prions -- Genetic aspects, Prions -- Research, Health, Psychology and mental health
Published: 2009

Author: Morgia, C. La, Parchi, P., Capellari, S., Lodi, R., Tonon, C., Rinaldi, R., Mondini, S., and Cirignotta, F.
Subjects: Creutzfeldt-Jakob disease -- Diagnosis, Creutzfeldt-Jakob disease -- Case studies, Autopsy -- Usage, Health, Psychology and mental health
Published: 2009

Author: Parchi, P., Capellari, S., Chen, S.G., Petersen, R.B., Gambetti, P., Kopp, N., Brown, P., Kitamoto, T., Tateishi, J., Giese, A., and Kretzschmar, H.
Subjects: Prions -- Research, Creutzfeldt-Jakob disease -- Development and progression, Pathogenic microorganisms -- Research, Environmental issues, Science and technology, Zoology and wildlife conservation
Abstract: The pathogenesis of prion diseases is centered on the conversion of the cellular prion protein (PrP(supra C)) into the pathological and protease-resistant isoform (PrP(supra res)). The conversion results in PrP (supra res) types that have distinct physical and chemical characteristics. An observation of the types of PrP (supra res) in sporadic Creutzfeldt-Jakob disease, iatrogenic CJD (iCJD), and the new variant CJD (vCJD) shows that iCJD and vCJD reveals only two patterns of electrophoretic mobility.
Published: 1997

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