Foto del docente

Piero Parchi

Associate Professor

Department of Biomedical and Neuromotor Sciences

Academic discipline: MED/26 Neurology

Publications

Abu-Rumeileh S.; Oeckl P.; Baiardi S.; Halbgebauer S.; Steinacker P.; Capellari S.; Otto M.; Parchi P., Csf ubiquitin levels are higher in alzheimer’s disease than in frontotemporal dementia and reflect the molecular subtype in prion disease, «BIOMOLECULES», 2020, 10, Article number: 497 , pp. 497 - 508 [Scientific article]Open Access

Mammana A.; Baiardi S.; Rossi M.; Franceschini A.; Donadio V.; Capellari S.; Caughey B.; Parchi P., Detection of prions in skin punch biopsies of Creutzfeldt–Jakob disease patients, «ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY», 2020, 7, pp. 559 - 564 [Scientific article]Open Access

Abu-Rumeileh, Samir; Vacchiano, Veria; Zenesini, Corrado; Polischi, Barbara; de Pasqua, Silvia; Fileccia, Enrico; Mammana, Angela; Di Stasi, Vitantonio; Capellari, Sabina; Salvi, Fabrizio; Liguori, Rocco; Parchi, Piero; BoReALS; Avoni, Patrizia, Diagnostic-prognostic value and electrophysiological correlates of CSF biomarkers of neurodegeneration and neuroinflammation in amyotrophic lateral sclerosis, «JOURNAL OF NEUROLOGY», 2020, 267, pp. 1699 - 1708 [Scientific article]Open Access

Raggi A.; Bartoletti-Stella A.; Parchi P.; Capellari S., First case of an UBQLN2 gene mutation causing frontotemporal dementia preceded by adult onset psychiatric symptoms, «AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION», 2020, 21, pp. 467 - 469 [Scientific article]

Melis M.; Molari A.; Floris G.; Vascellari S.; Balestrino L.; Ladogana A.; Poleggi A.; Parchi P.; Cossu G.; Melis M.; Orru S.; Defazio G., Genetic Creutzfeldt-Jakob disease in Sardinia: a case series linked to the PRNP R208H mutation due to a single founder effect, «NEUROGENETICS», 2020, 21, pp. 251 - 257 [Scientific article]

Baiardi S.; Rizzi R.; Capellari S.; Bartoletti-Stella A.; Zangrandi A.; Gasparini F.; Ghidoni E.; Parchi P., Gerstmann-Straüssler-Scheinker disease (PRNP p.D202N) presenting with atypical parkinsonism, «NEUROLOGY. GENETICS», 2020, 6, Article number: e400 , pp. 1 - 5 [Scientific article]Open Access

Jones E.; Hummerich H.; Vire E.; Uphill J.; Dimitriadis A.; Speedy H.; Campbell T.; Norsworthy P.; Quinn L.; Whitfield J.; Linehan J.; Jaunmuktane Z.; Brandner S.; Jat P.; Nihat A.; How Mok T.; Ahmed P.; Collins S.; Stehmann C.; Sarros S.; Kovacs G.G.; Geschwind M.D.; Golubjatnikov A.; Frontzek K.; Budka H.; Aguzzi A.; Karamujic-Comic H.; van der Lee S.J.; Ibrahim-Verbaas C.A.; van Duijn C.M.; Sikorska B.; Golanska E.; Liberski P.P.; Calero M.; Calero O.; Sanchez-Juan P.; Salas A.; Martinon-Torres F.; Bouaziz-Amar E.; Haik S.; Laplanche J.-L.; Brandel J.-P.; Amouyel P.; Lambert J.-C.; Parchi P.; Bartoletti-Stella A.; Capellari S.; Poleggi A.; Ladogana A.; Pocchiari M.; Aneli S.; Matullo G.; Knight R.; Zafar S.; Zerr I.; Booth S.; Coulthart M.B.; Jansen G.H.; Glisic K.; Blevins J.; Gambetti P.; Safar J.; Appleby B.; Collinge J.; Mead S., Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study, «LANCET NEUROLOGY», 2020, 19, pp. 840 - 848 [Scientific article]

Zucchi E.; Bonetto V.; Soraru G.; Martinelli I.; Parchi P.; Liguori R.; Mandrioli J., Neurofilaments in motor neuron disorders: towards promising diagnostic and prognostic biomarkers, «MOLECULAR NEURODEGENERATION», 2020, 15, Article number: 58 , pp. 58 - 58 [Scientific article]Open Access

Puopolo M.; Catelan D.; Capellari S.; Ladogana A.; Sanguedolce A.; Fedele A.; Aprile V.; Turco G.L.; Colaizzo E.; Tiple D.; Vaianella L.; Parchi P.; Biggeri A.; Pocchiari M., Spatial Epidemiology of Sporadic Creutzfeldt-Jakob Disease in Apulia, Italy, «NEUROEPIDEMIOLOGY», 2020, 54, pp. 83 - 89 [Scientific article]

Calandra Buonaura G.; Sambati L.; Baschieri F.; Vitiello M.; Contin M.; Tonon C.; Capellari S.; Provini F.; Cortelli P.; Barletta G.; Caltabiano G.; Cecere A.; Gallassi R.; Giannini G.; Guaraldi P.; Lodi R.; Lopane G.; Manners D.N.; Martinelli P.; Miele F.; Mignani F.; Mohamed S.; Nassetti S.; Oppi F.; Parchi P.; Pierangeli G.; Poda R.; Scaglione C.; Solieri L.; Stanzani Maserati M.; Testa C., The Bologna motor and non-motor prospective study on parkinsonism at onset (BoProPark): study design and population, «NEUROLOGICAL SCIENCES», 2020, 41, pp. 2531 - 2537 [Scientific article]Open Access

Candelise N.; Baiardi S.; Franceschini A.; Rossi M.; Parchi P., Towards an improved early diagnosis of neurodegenerative diseases: The emerging role of in vitro conversion assays for protein amyloids, «ACTA NEUROPATHOLOGICA COMMUNICATIONS», 2020, 8, Article number: 117 , pp. 117 - 133 [Scientific article]Open Access

Rossi M.; Candelise N.; Baiardi S.; Capellari S.; Giannini G.; Orru C.D.; Antelmi E.; Mammana A.; Hughson A.G.; Calandra-Buonaura G.; Ladogana A.; Plazzi G.; Cortelli P.; Caughey B.; Parchi P., Ultrasensitive RT-QuIC assay with high sensitivity and specificity for Lewy body-associated synucleinopathies, «ACTA NEUROPATHOLOGICA», 2020, 140, pp. 49 - 62 [Scientific article]Open Access

Areskeviciute A.; Hogh P.; Bartoletti-Stella A.; Melchior L.C.; Nielsen P.R.; Parchi P.; Capellari S.; Broholm H.; Scheie D.; Lund E.L., A Novel Eight Octapeptide Repeat Insertion in PRNP Causing Prion Disease in a Danish Family, «JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY», 2019, 78, pp. 595 - 604 [Scientific article]

Minikel E.V.; Vallabh S.M.; Orseth M.C.; Brandel J.-P.; Haik S.; Laplanche J.-L.; Zerr I.; Parchi P.; Capellari S.; Safar J.; Kenny J.; Fong J.C.; Takada L.T.; Ponto C.; Hermann P.; Knipper T.; Stehmann C.; Kitamoto T.; Ae R.; Hamaguchi T.; Sanjo N.; Tsukamoto T.; Mizusawa H.; Collins S.J.; Chiesa R.; Roiter I.; de Pedro-Cuesta J.; Calero M.; Geschwind M.D.; Yamada M.; Nakamura Y.; Mead S., Age at onset in genetic prion disease and the design of preventive clinical trials, «NEUROLOGY», 2019, 93, pp. e125 - e134 [Scientific article]Open Access

Bartoletti-Stella A.; Corrado P.; Mometto N.; Baiardi S.; Durrenberger P.F.; Arzberger T.; Reynolds R.; Kretzschmar H.; Capellari S.; Parchi P., Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease, «MOLECULAR NEUROBIOLOGY», 2019, 56, pp. 5009 - 5024 [Scientific article]Open Access

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