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Piero Parchi

Associate Professor

Department of Experimental, Diagnostic and Specialty Medicine - DIMES

Academic discipline: MED/26 Neurology

Publications

Francesca, Lattanzio; Samir, Abu-Rumeileh; Alessia, Franceschini; Hideaki, Kai; Giulia, Amore; Ilaria, Poggiolini; Marcello, Rossi; Simone, Baiardi; Lynne, Mcguire; Anna, Ladogana; Maurizio, Pocchiari; Alison, Green; Sabina, Capellari; Piero, Parchi, Prion-specific and surrogate CSF biomarkers in Creutzfeldt-Jakob disease: diagnostic accuracy in relation to molecular subtypes and analysis of neuropathological correlates of p-tau and A$\upbeta$42 levels, «ACTA NEUROPATHOLOGICA», 2017, 133, pp. 559 - 578 [Scientific article]

Baiardi, Simone; Magherini, Anna; Capellari, Sabina; Redaelli, Veronica; Ladogana, Anna; Rossi, Marcello; Tagliavini, Fabrizio; Pocchiari, Maurizio; Giaccone, Giorgio; Parchi, Piero, Towards an early clinical diagnosis of sporadic CJD VV2 (ataxic type), «JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY», 2017, 88, pp. 764 - 772 [Scientific article]

Cescatti, Maura; Saverioni, Daniela; Capellari, Sabina; Tagliavini, Fabrizio; Kitamoto, Tetsuyuki; Ironside, James; Giese, Armin; Parchi, Piero, Analysis of Conformational Stability of Abnormal Prion Protein Aggregates across the Spectrum of Creutzfeldt-Jakob Disease Prions, «JOURNAL OF VIROLOGY», 2016, 90, pp. 6244 - 6254 [Scientific article]

Mcguire, Lynne I.; Poleggi, Anna; Poggiolini, Ilaria; Suardi, Silvia; Grznarova, Katarina; Shi, Song; de Vil, Bart; Sarros, Shannon; Satoh, Katsuya; Cheng, Keding; Cramm, Maria; Fairfoul, Graham; Schmitz, Matthias; Zerr, Inga; Cras, Patrick; Equestre, Michele; Tagliavini, Fabrizio; Atarashi, Ryuichiro; Knox, David; Collins, Steven; Haïk, Stéphane; Parchi, Piero; Pocchiari, Maurizio; Green, Alison, Cerebrospinal fluid real-time quaking-induced conversion is a robust and reliable test for sporadic creutzfeldt–jakob disease: An international study, «ANNALS OF NEUROLOGY», 2016, 80, pp. 160 - 165 [Scientific article]

Takeuchi, Atsuko; Kobayashi, Atsushi; Parchi, Piero; Yamada, Masahito; Morita, Masanori; Uno, Shusei; Kitamoto, Tetsuyuki, Distinctive properties of plaque-type dura mater graft-associated Creutzfeldt–Jakob disease in cell-protein misfolding cyclic amplification, «LABORATORY INVESTIGATION», 2016, 96, pp. 581 - 587 [Scientific article]

Minikel, Eric Vallabh; Vallabh, Sonia M.; Lek, Monkol; Estrada, Karol; Samocha, Kaitlin E.; Sathirapongsasuti, J. Fah; Mclean, Cory Y.; Tung, Joyce Y.; Yu, Linda P. C.; Gambetti, Pierluigi; Blevins, Janis; Zhang, Shulin; Cohen, Yvonne; Chen, Wei; Yamada, Masahito; Hamaguchi, Tsuyoshi; Sanjo, Nobuo; Mizusawa, Hidehiro; Nakamura, Yosikazu; Kitamoto, Tetsuyuki; Collins, Steven J.; Boyd, Alison; Will, Robert G.; Knight, Richard; Ponto, Claudia; Zerr, Inga; Kraus, Theo F.J.; Eigenbrod, Sabina; Giese, Armin; Calero, Miguel; De Pedro-Cuesta, Jesús; Haïk, Stéphane; Laplanche, Jean-Louis; Bouaziz-Amar, Elodie; Brandel, Jean-Philippe; Capellari, Sabina; Parchi, Piero; Poleggi, Anna; Ladogana, Anna; O'Donnell-Luria, Anne H.; Karczewski, Konrad J.; Marshall, Jamie L.; Boehnke, Michael; Laakso, Markku; Mohlke, Karen L.; Kähler, Anna; Chambert, Kimberly; Mccarroll, Steven; Sullivan, Patrick F.; Hultman, Christina M.; Purcell, Shaun M.; Sklar, Pamela; Van Der Lee, Sven J.; Rozemuller, Annemieke; Jansen, Casper; Hofman, Albert; Kraaij, Robert; Van Rooij, Jeroen G. J.; Ikram, M. Arfan; Uitterlinden, André G.; Van Duijn, Cornelia M.; Daly, Mark J.; Macarthur, Daniel G., Quantifying prion disease penetrance using large population control cohorts, «SCIENCE TRANSLATIONAL MEDICINE», 2016, 8, pp. 9 - 20 [Scientific article]

Baiardi, Simone; Capellari, Sabina; Ladogana, Anna; Strumia, Silvia; Santangelo, Mario; Pocchiari, Maurizio; Parchi, Piero, Revisiting the Heidenhain Variant of Creutzfeldt-Jakob Disease: Evidence for Prion Type Variability Influencing Clinical Course and Laboratory Findings, «JOURNAL OF ALZHEIMER'S DISEASE», 2016, 50, pp. 465 - 476 [Scientific article]

Bartoletti-Stella A; Gasparini L; Giacomini C; Corrado P; Terlizzi R; Giorgio E; Magini P; Seri M; Baruzzi A; Parchi P; Brusco A; Cortelli P; Capellari S, Messenger RNA processing is altered in autosomal dominant leukodystrophy, «HUMAN MOLECULAR GENETICS», 2015, 24, pp. 2746 - 2756 [Scientific article]

Alafuzoff, Irina; Pikkarainen, Maria; Neumann, Manuela; Arzberger, Thomas; Al-Sarraj, Safa; Bodi, Istvan; Bogdanovic, Nenad; Bugiani, Orso; Ferrer, Isidro; Gelpi, Ellen; Gentleman, Stephen; Giaccone, Giorgio; Graeber, Manuel B.; Hortobagyi, Tibor; Ince, Paul G.; Ironside, James W.; Kavantzas, Nikolaos; King, Andrew; Korkolopoulou, Penelope; Kovács, Gábor G.; Meyronet, David; Monoranu, Camelia; Nilsson, Tatjana; Parchi, Piero; Patsouris, Efstratios; Revesz, Tamas; Roggendorf, Wolfgang; Rozemuller, Annemieke; Seilhean, Danielle; Streichenberger, Nathalie; Thal, Dietmar R.; Wharton, Stephen B.; Kretzschmar, Hans, Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium, «JOURNAL OF NEURAL TRANSMISSION», 2015, 122, pp. 957 - 972 [Scientific article]

Kobayashi, Atsushi; Parchi, Piero; Yamada, Masahito; Brown, Paul; Saverioni, Daniela; Matsuura, Yuichi; Takeuchi, Atsuko; Mohri, Shirou; Kitamoto, Tetsuyuki, Transmission properties of atypical Creutzfeldt-Jakob disease: A clue to disease etiology?, «JOURNAL OF VIROLOGY», 2015, 89, pp. 3939 - 3946 [Scientific article]

Bacchelli E;Ceroni F;Pinto D;Lomartire S;Giannandrea M;D'Adamo P;Bonora E;Parchi P;Tancredi R;Battaglia A;Maestrini E, A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder., «JOURNAL OF NEURODEVELOPMENTAL DISORDERS», 2014, 6, pp. 1 - 11 [Scientific article]Open Access

Cortelli, P.; Fabbri, M.; Calandra-Buonaura, G.; Capellari, S.; Tinuper, P.; Parchi, P.; Lugaresi, E., Gait disorders in fatal familial insomnia, «MOVEMENT DISORDERS», 2014, 29, pp. 420 - 424 [Scientific article]

Bonora E;Graziano C;Minopoli F;Bacchelli E;Magini P;Diquigiovanni C;Lomartire S;Bianco F;Vargiolu M;Parchi P;Marasco E;Mantovani V;Rampoldi L;Trudu M;Parmeggiani A;Battaglia A;Mazzone L;Tortora G;Maestrini E;Seri M;Romeo G;IMGSAC, Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients., «EMBO MOLECULAR MEDICINE», 2014, 6, pp. 795 - 809 [Scientific article]Open Access

Franco Cardone; Serena Principe; Maria Eugenia Schininà; Bruno Maras; Sabina Capellari; Piero Parchi; Silvio Notari; Laura Di Francesco; Anna Poleggi; Roberta Galeno; Ramona Vinci; Vittorio Mellina; Susanna Almonti; Anna Ladogana; Maurizio Pocchiari, Mutant PrPCJD prevails over wild-type PrPCJD in the brain of V210I and R208H genetic Creutzfeldt-Jakob disease patients, «BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS», 2014, 454, pp. 289 - 294 [Scientific article]

Moghadam KK;Pizza F;La Morgia C;Franceschini C;Tonon C;Lodi R;Barboni P;Seri M;Ferrari S;Liguori R;Donadio V;Parchi P;Cornelio F;Inzitari D;Mignarri A;Capocchi G;Dotti MT;Winkelmann J;Lin L;Mignot E;Carelli V;Plazzi G, Narcolepsy is a common phenotype in HSAN IE and ADCA-DN, «BRAIN», 2014, 137, pp. 1643 - 1655 [Scientific article]

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