Foto del docente

Piero Parchi

Professore associato

Dipartimento di Scienze Biomediche e Neuromotorie

Settore scientifico disciplinare: MED/26 NEUROLOGIA

Pubblicazioni

Poleggi, Anna; van der Lee, Sven; Capellari, Sabina; Puopolo, Maria; Ladogana, Anna; De Pascali, Eleonora; Lia, Debora; Formato, Alessia; Bartoletti-Stella, Anna; Parchi, Piero; van Duijn, Cornelia; Pocchiari, Maurizio, Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by theCYP4X1gene, «JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY», 2018, 89, pp. 1243 - 1249 [articolo]

Iaccarino, Leonardo; Presotto, Luca; Bettinardi, Valentino; Gianolli, Luigi; Roiter, Ignazio; Capellari, Sabina; Parchi, Piero; Cortelli, Pietro; Perani, Daniela, An in vivo 11C-PK PET study of microglia activation in Fatal Familial Insomnia, «ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY», 2018, 5, pp. 11 - 18 [articolo]Open Access

Abu-Rumeileh, Samir; Mometto, Nicola; Bartoletti-Stella, Anna; Polischi, Barbara; Oppi, Federico; Poda, Roberto; Stanzani-Maserati, Michelangelo; Cortelli, Pietro; Liguori, Rocco; Capellari, Sabina; Parchi, Piero, Cerebrospinal fluid biomarkers in patients with frontotemporal dementia spectrum: A single-center study, «JOURNAL OF ALZHEIMER'S DISEASE», 2018, 66, pp. 551 - 563 [articolo]

Abu-Rumeileh, Samir; Baiardi, Simone; D'Angelo, Roberto; Dentale, Nicola; Fasulo, Giovanni; Guarino, Maria; Parchi, Piero, Clinical Reasoning: Rapidly progressive dementia in a patient with HIV after an exotic journey, «NEUROLOGY», 2018, 91, pp. e1360 - e1364 [articolo]

Race, Brent; Williams, Katie; Hughson, Andrew G.; Jansen, Casper; Parchi, Piero; Rozemuller, Annemieke J. M.; Chesebro, Bruce, Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein, «ACTA NEUROPATHOLOGICA COMMUNICATIONS», 2018, 6, Article number: 13, pp. 1 - 16 [articolo]Open Access

Cali, Ignazio; Cohen, Mark L.; Haїk, Stéphane; Parchi, Piero; Giaccone, Giorgio; Collins, Steven J.; Kofskey, Diane; Wang, Han; McLean, Catriona A.; Brandel, Jean-Philippe; Privat, Nicolas; Sazdovitch, Véronique; Duyckaerts, Charles; Kitamoto, Tetsuyuki; Belay, Ermias D.; Maddox, Ryan A.; Tagliavini, Fabrizio; Pocchiari, Maurizio; Leschek, Ellen; Appleby, Brian S.; Safar, Jiri G.; Schonberger, Lawrence B.; Gambetti, Pierluigi, Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study, «ACTA NEUROPATHOLOGICA COMMUNICATIONS», 2018, 6, Article number: 5, pp. 1 - 19 [articolo]Open Access

Bartoletti-Stella, Anna; Baiardi, Simone; Stanzani-Maserati, Michelangelo; Piras, Silvia; Caffarra, Paolo; Raggi, Alberto; Pantieri, Roberta; Baldassari, Sara; Caporali, Leonardo; Abu-Rumeileh, Samir; Linarello, Simona; Liguori, Rocco; Parchi, Piero; Capellari, Sabina, Identification of rare genetic variants in Italian patients with dementia by targeted gene sequencing, «NEUROBIOLOGY OF AGING», 2018, 66, pp. e23 - e31 [articolo]

Quadri, Marialuisa; Mandemakers, Wim; Grochowska, Martyna M; Masius, Roy; Geut, Hanneke; Fabrizio, Edito; Breedveld, Guido J; Kuipers, Demy; Minneboo, Michelle; Vergouw, Leonie J M; Carreras Mascaro, Ana; Yonova-Doing, Ekaterina; Simons, Erik; Zhao, Tianna; Di Fonzo, Alessio B; Chang, Hsiu-Chen; Parchi, Piero; Melis, Marta; Correia Guedes, Leonor; Criscuolo, Chiara; Thomas, Astrid; Brouwer, Rutger W W; Heijsman, Daphne; Ingrassia, Angela M T; Calandra Buonaura, Giovanna; Rood, Janneke P; Capellari, Sabina; Rozemuller, Annemieke J; Sarchioto, Marianna; Fen Chien, Hsin; Vanacore, Nicola; Olgiati, Simone; Wu-Chou, Yah-Huei; Yeh, Tu-Hsueh; Boon, Agnita J W; Hoogers, Susanne E; Ghazvini, Mehrnaz; IJpma, Arne S; van IJcken, Wilfred F J; Onofrj, Marco; Barone, Paolo; Nicholl, David J; Puschmann, Andreas; De Mari, Michele; Kievit, Anneke J; Barbosa, Egberto; De Michele, Giuseppe; Majoor-Krakauer, Danielle; van Swieten, John C; de Jong, Frank J; Ferreira, Joaquim J; Cossu, Giovanni; Lu, Chin-Song; Meco, Giuseppe; Cortelli, Pietro; van de Berg, Wilma D J; Bonifati, Vincenzo*, LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study, «LANCET NEUROLOGY», 2018, 17, pp. 597 - 608 [articolo]

Abu-Rumeileh, Samir; Capellari, Sabina; Parchi, Piero, Rapidly Progressive Alzheimer’s Disease: Contributions to Clinical-Pathological Definition and Diagnosis, «JOURNAL OF ALZHEIMER'S DISEASE», 2018, 63, pp. 887 - 897 [articolo]

Franceschini, A.; Strammiello, R.; Capellari, S.; Giese, A.; Parchi, P., Regional pattern of microgliosis in sporadic Creutzfeldt-Jakob disease in relation to phenotypic variants and disease progression, «NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY», 2018, 44, pp. 574 - 589 [articolo]

Zerr, Inga; Parchi, Piero, Sporadic Creutzfeldt–Jakob disease, in: Human Prion Diseases, Amsterdam, Netherlands, Elsevier, 2018, pp. 155 - 174 (HANDBOOK OF CLINICAL NEUROLOGY) [capitolo di libro]

Abu-Rumeileh, Samir; Redaelli, Veronica; Baiardi, Simone; Mackenzie, Graeme; Windl, Otto; Ritchie, Diane L; Didato, Giuseppe; Hernandez-Vara, Jorge; Rossi, Marcello; Capellari, Sabina; Imperiale, Daniele; Rizzone, Mario Giorgio; Belotti, Alessia; Sorbi, Sandro; Rozemuller, Annemieke J M; Cortelli, Pietro; Gelpi, Ellen; Will, Robert G; Zerr, Inga; Giaccone, Giorgio; Parchi, Piero, Sporadic Fatal Insomnia in Europe: Phenotypic features and diagnostic challenges, «ANNALS OF NEUROLOGY», 2018, 84, pp. 347 - 360 [articolo]

Abu-Rumeileh, Samir; Capellari, Sabina; Stanzani-Maserati, Michelangelo; Polischi, Barbara; Martinelli, Paolo; Caroppo, Paola; Ladogana, Anna; Parchi, Piero, The CSF neurofilament light signature in rapidly progressive neurodegenerative dementias, «ALZHEIMER'S RESEARCH & THERAPY», 2018, 10, Article number: 3, pp. 1 - 11 [articolo]Open Access

Giannoccaro, Maria Pia; Bartoletti-Stella, Anna; Piras, Silvia; Casalena, Alfonsina; Oppi, Federico; Ambrosetto, Giovanni; Montagna, Pasquale; Liguori, Rocco; Parchi, Piero; Capellari, Sabina, The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance, «JOURNAL OF ALZHEIMER'S DISEASE», 2018, 62, pp. 687 - 697 [articolo]

Capellari, Sabina; Baiardi, Simone; Rinaldi, Rita; Bartoletti-Stella, Anna; Graziano, Claudio; Piras, Silvia; Calandra-Buonaura, Giovanna; D'Angelo, Roberto; Terziotti, Camilla; Lodi, Raffaele; Donadio, Vincenzo; Pironi, Loris; Cortelli, Pietro; Parchi, Piero, Two novel PRNP truncating mutations broaden the spectrum of prion amyloidosis, «ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY», 2018, 5, pp. 777 - 783 [articolo]Open Access

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