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Parchi P.; Saverioni D., Molecular pathology, classification, and diagnosis of sporadic human prion disease variants., «FOLIA NEUROPATHOLOGICA», 2012, 50, pp. 20 - 45 [articolo]
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Jansen C.; Voet W.; Head M.W.; Parchi P.; Yull H.; Verrips A.; Wesseling P.; Meulstee J.; Baas F.; van Gool W.A.; Ironside J.W.; Rozemuller A.J., A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Straussler-Scheinker disease phenotype: comparison with similar cases from the literature., «ACTA NEUROPATHOLOGICA», 2011, 121, pp. 59 - 68 [articolo]
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Parchi P.; Capellari S.; Gambetti P., Fatal Familial and Sporadic Insomnia., in: Esperti Internazionali (N=99), Neurodegeneration:The molecular pathology of dementia and movement disorders., CHICHESTER, Wiley-Blackwell, 2011, pp. 346 - 349 [capitolo di libro]
Parchi P.; Gambetti P.; Capellari S., Genetic Creutzfeldt-Jakob Disease., in: Neurodegeneration: The molecular pathology of dementia and movement disorders., CHICHESTER, Wiley-Blackwell, 2011, pp. 336 - 345 [capitolo di libro]
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Parchi P.; Strammiello R.; Giese A.; Kretzschmar H., Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future., «ACTA NEUROPATHOLOGICA», 2011, 121, pp. 91 - 112 [articolo]
Budka H.; Head M.W.; Ironside J.W.; Gambetti P.; Parchi P.; Tagliavini F., Sporadic Creutzfeldt-Jakob Disease., in: Esperti Internazionali (N=99), Neurodegeneration: The molecular pathology of dementia and movement disorders -Second Edition, CHICHESTER, Wiley-Blackwell, 2011, pp. 322 - 335 [capitolo di libro]
Parchi P.; Cescatti M.; Notari S.; Schulz-Schaeffer W.J.; Capellari S.; Giese A.; Zou W.Q.; Kretzschmar H.; Ghetti B.; Brown P., Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease., «BRAIN», 2010, 133, pp. 3030 - 3042 [articolo]
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Jansen C.; Parchi P.; Capellari S.; Vermeij A.J.; Corrado P.; Baas F.; Strammiello R.; van Gool W.A.; van Swieten J.C.; Rozemuller A.J., Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP., «ACTA NEUROPATHOLOGICA», 2010, 119, pp. 189 - 197 [articolo]
