Foto del docente

Piero Parchi

Professore associato

Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale

Settore scientifico disciplinare: MED/26 NEUROLOGIA


Jansen C.; Parchi P.; Capellari S.; Ibrahim-Verbaas C.A.; Schuur M.; Strammiello R.; Corrado P.; Bishop M.T.; van Gool W.A.; Verbeek M.M.; Baas F.; van Saane W.; Spliet W.G.; Jansen G.H.; van Duijn C.M.; Rozemuller A.J., Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects., «PLOS ONE», 2012, 7, pp. 1 - 10 [articolo]

Parchi P.; Saverioni D., Molecular pathology, classification, and diagnosis of sporadic human prion disease variants., «FOLIA NEUROPATHOLOGICA», 2012, 50, pp. 20 - 45 [articolo]

Durrenberger P.F.; Fernando F.S.; Magliozzi R.; Kashefi S.N.; Bonnert T.P.; Ferrer I.; Seilhean D.; Nait-Oumesmar B.; Schmitt A.; Gebicke-Haerter P.J.; Falkai P.; Grünblatt E.; Palkovits M.; Parchi P.; Capellari S.; Arzberger T.; Kretzschmar H.; Roncaroli F.; Dexter D.T.; Reynolds R., Selection of novel reference genes for use in the human central nervous system: a BrainNet Europe Study., «ACTA NEUROPATHOLOGICA», 2012, 124, pp. 893 - 903 [articolo]

Alafuzoff I.; Gelpi E.; Al-Sarraj S.; Arzberger T.; Attems J.; Bodi I.; Bogdanovic N.; Budka H.; Bugiani O.; Englund E.; Ferrer I.; Gentleman S.; Giaccone G.; Graeber M.B.; Hortobagyi T.; Höftberger R.; Ironside J.W.; Jellinger K.; Kavantzas N.; King A.; Korkolopoulou P.; Kovács G.G.; Meyronet D.; Monoranu C.; Parchi P.; Patsouris E.; Roggendorf W.; Rozemuller A.; Seilhean D.; Streichenberger N.; Thal D.R.; Wharton S.B.; Kretzschmar H., The need to unify neuropathological assessments of vascular alterations in the ageing brain: Multicentre survey by the BrainNet Europe consortium., «EXPERIMENTAL GERONTOLOGY», 2012, 47, pp. 825 - 833 [articolo]

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]

Jansen C.; Parchi P.; Capellari S.; Strammiello R.; Dopper E.G.; van Swieten J.C.; Kamphorst W.; Rozemuller A.J., A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient., «JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY», 2011, 70, pp. 698 - 702 [articolo]

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]

Capellari S.; Strammiello R.; Saverioni D.; Kretzschmar H.; Parchi P., Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: Insights into phenotypic variability and disease pathogenesis., «ACTA NEUROPATHOLOGICA», 2011, 121, pp. 21 - 37 [articolo]

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]

Notari S.; Moleres F.J.; Hunter S.B.; Belay E.D.; Schonberger L.B.; Cali I.; Parchi P.; Shieh W.J.; Brown P.; Zaki S.; Zou W.Q.; Gambetti P., Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States., «PLOS ONE», 2010, 5, pp. 1 - 8 [articolo]

Zou W.Q.; Langeveld J.; Xiao X.; Chen S.; McGeer P.L.; Yuan J.; Payne M.C.; Kang H.E.; McGeehan J.; Sy M.S.; Greenspan N.S.; Kaplan D.; Wang G.X.; Parchi P.; Hoover E.; Kneale G.; Telling G.; Surewicz W.K.; Kong Q.; Guo J.P., PrP conformational transitions alter species preference of a PrP-specific antibody., «THE JOURNAL OF BIOLOGICAL CHEMISTRY», 2010, 285, pp. 13874 - 13884 [articolo]

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]

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