Foto del docente

Piero Parchi

Professore associato

Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale

Settore scientifico disciplinare: MED/26 NEUROLOGIA

Pubblicazioni

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, pp. 1 - 11 [articolo]

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]

Baiardi, Simone; Capellari, Sabina; Bartoletti Stella, Anna; Parchi, Piero, Unusual Clinical Presentations Challenging the Early Clinical Diagnosis of Creutzfeldt-Jakob Disease, «JOURNAL OF ALZHEIMER'S DISEASE», 2018, 64, pp. 1051 - 1065 [articolo]

Vicente-Pascual, Mikel; Rossi, Marcello; Gámez, Josep; Lladó, Albert; Valls, Josep; Grau-Rivera, Oriol; Ávila Polo, Rainiero; Llorens, Franc; Zerr, Inga; Ferrer, Isidre; Nos, Carlos; Parchi, Piero; Sánchez-Valle, Raquel; Gelpí, Ellen, Variably protease-sensitive prionopathy presenting within ALS/FTD spectrum, «ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY», 2018, 5, pp. 1297 - 1302 [articolo]

Rossi, Marcello; Saverioni, Daniela; Di Bari, Michele; Baiardi, Simone; Lemstra, Afina Willemina; Pirisinu, Laura; Capellari, Sabina; Rozemuller, Annemieke; Nonno, Romolo; Parchi, Piero, Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature, «ACTA NEUROPATHOLOGICA COMMUNICATIONS», 2017, 5, pp. 1 - 12 [articolo]

Bartoletti-Stella, Anna; Gasparini, Laura; Giacomini, Caterina; Corrado, Patrizia; Terlizzi, Rossana; Giorgio, Elisa; Magini, Pamela; Seri, Marco; Baruzzi, Agostino; Parchi, Piero; Brusco, Alfredo; Cortelli, Pietro; Capellari, Sabina, Corrigendum: Messenger RNA processing is altered in autosomal dominant leukodystrophy [Human Molecular Genetics, 24 (2015) (2746-2756)] DOI:10.1093/hmg/ddv034, «HUMAN MOLECULAR GENETICS», 2017, 26, pp. 3868 - 3868 [articolo]

Abu Rumeileh, Samir; Lattanzio, Francesca; Stanzani Maserati, Michelangelo; Rizzi, Romana; Capellari, Sabina; Parchi, Piero, Diagnostic Accuracy of a Combined Analysis of Cerebrospinal Fluid t-PrP, t-tau, p-tau, and Aβ42 in the Differential Diagnosis of Creutzfeldt-Jakob Disease from Alzheimer's Disease with Emphasis on Atypical Disease Variants, «JOURNAL OF ALZHEIMER'S DISEASE», 2017, 55, pp. 1471 - 1480 [articolo]

Franceschini, Alessia; Baiardi, Simone; Hughson, Andrew G.; Mckenzie, Neil; Moda, Fabio; Rossi, Marcello; Capellari, Sabina; Green, Alison; Giaccone, Giorgio; Caughey, Byron; Parchi, Piero, High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions, «SCIENTIFIC REPORTS», 2017, 7, pp. 1 - 8 [articolo]

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