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 [articolo]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 [articolo]
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 [articolo]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 [articolo]
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 [articolo]
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 [articolo]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 [articolo]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 [articolo]
Giannini, G.; Palandri, G.; Ferrari, A.; Oppi, F.; Milletti, D.; Albini-Riccioli, L.; Mantovani, P.; Magnoni, S.; Chiari, L.; Cortelli, P.; Cevoli, S.; Agati, R.; Calandra-Buonaura, G.; Capellari, S.; Parchi, P.; Stanzani-Maserati, M.; Marliani, A. F.; Merola, M.; Piserchia, V. A.; Sambati, L.; Sturiale, C.; Supino, A.; Nicola, M.; Urli, T., A prospective evaluation of clinical and instrumental features before and after ventriculo-peritoneal shunt in patients with idiopathic Normal pressure hydrocephalus: The Bologna PRO-Hydro study, «PARKINSONISM & RELATED DISORDERS», 2019, 66, pp. 117 - 124 [articolo]
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 [articolo]Open Access
Giorgio, E.; Lorenzati, M.; Di Val Cervo, P. R.; Brussino, A.; Cernigoj, M.; Sala, E. D.; Stella, A. B.; Ferrero, M.; Caiazzo, M.; Capellari, S.; Cortelli, P.; Conti, L.; Cattaneo, E.; Buffo, A.; Brusco, A., Allele-specific silencing as treatment for gene duplication disorders: Proof-of-principle in autosomal dominant leukodystrophy, «BRAIN», 2019, 142, pp. 1905 - 1920 [articolo]
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 [articolo]Open Access
Baiardi S.; Abu-Rumeileh S.; Rossi M.; Zenesini C.; Bartoletti-Stella A.; Polischi B.; Capellari S.; Parchi P., Antemortem CSF Aβ42/Aβ40 ratio predicts Alzheimer's disease pathology better than Aβ42 in rapidly progressive dementias, «ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY», 2019, 6, pp. 263 - 273 [articolo]Open Access
Oosterloo, Mayke; Bijlsma, Emilia K.; van Kuijk, Sander MJ.; Minkels, Floor; de Die-Smulders, Christine EM.; Bachoud-Lévi, Anne-Catherine; Bentivoglio, Anna-Rita; Biunno, Ida; Bonelli, Raphael M.; Bronzova, Juliana; Burgunder, Jean-Marc; Dunnett, Stephen B.; Ferreira, Joaquim J.; Frich, Jan; Giuliano, Joe; Handley, Olivia J.; Heiberg, Arvid; Illarioshkin, Sergey; Illmann, Torsten; Klempir, Jiri; Landwehrmeyer, G. Bernhard; Levey, Jamie; McLean, Tim; Nielsen, Jørgen E.; Koivisto, Susana Pro; Päivärinta, Markku; Pålhagen, Sven; Quarrell, Oliver; Ramos-Arroyo, Maria; Roos, Raymund A.C.; Saft, Carsten; Sebastián, Ana Rojo; Tabrizi, Sarah J.; Vandenberghe, Wim; Verellen-Dumoulin, Christine; Uhrova, Tereza; Wahlström+, Jan; Zaremba, Jacek; (formerly Rödig, Verena Baake; Barth, Katrin; Garde, Monica Bascuñana; Becanovic, Kristina; Bernard, Tomáš; Betz, Sabrina; Bos, Reineke; Come, Adrien; Guedes, Leonor Correia; Callaghan, Jenny; Capodarca, Selene; Charpentier, Sébastien; Vieira , Clinical and genetic characteristics of late-onset Huntington's disease, «PARKINSONISM & RELATED DISORDERS», 2019, 61, pp. 101 - 105 [articolo]
Contin, Manuela; Lopane, Giovanna; Mohamed, Susan; Calandra-Buonaura, Giovanna; Capellari, Sabina; De Massis, Patrizia; Nassetti, Stefania; Perrone, Alessandro; Riva, Roberto; Sambati, Luisa; Scaglione, Cesa; Cortelli, Pietro, Clinical pharmacokinetics of pramipexole, ropinirole and rotigotine in patients with Parkinson's disease, «PARKINSONISM & RELATED DISORDERS», 2019, 61, pp. 111 - 117 [articolo]
