Sabina Capellari

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, Article number: 10655, pp. 1 - 8 [articolo]Open Access

Moss, Davina J. Hensman; Tabrizi, Sarah J; Mead, Simon; Kitty, Lo; Pardiã±as, Antonio F; Holmans, Peter; Jones, Lesley; Langbehn, Douglas; Coleman, A.; Santos, R. Dar; Decolongon, J.; Sturrock, A.; Bardinet, E.; Ret, C. Jauff; Justo, D.; Lehericy, S.; Marelli, C.; Nigaud, K.; Valabrãgue, R.; van den Bogaard, S. J. A.; Dumas, E. M.; van der Grond, J.; T'Hart, E. P.; Jurgens, C.; Witjes-Ane, M. -. N.; Arran, N.; Callaghan, J.; Stopford, C.; Frost, C.; Jones, R.; Hobbs, N.; Lahiri, N.; Ordidge, R.; Owen, G.; Pepple, T.; Read, J.; Say, M.; Wild, E.; Patel, A.; Fox, N. C.; Gibbard, C.; Malone, I.; Crawford, H.; Whitehead, D.; Keenan, S.; Cash, D. M.; Berna, C.; Bechtel, N.; Bohlen, S.; Man, A. Hoff; Kraus, P.; Axelson, E.; Wang, C.; Acharya, T.; Lee, S.; Monaco, W.; Campbell, C.; Queller, S.; Whitlock, K.; Campbell, C.; Campbell, M.; Frajman, E.; Milchman, C.; O'Regan, A.; Labuschagne, I.; Stout, J.; Landwehrmeyer, B.; Craufurd, D.; Scahill, R.; Hicks, S.; Kennard, C.; Johnson, H.; Tobin, A.; Rosas, H. D.; Reilmann, R.; Borowsky, B.; Pourchot, C.; Andrews, S. C.; Bachoud-Lévi, Anne-Catherine; Bentivoglio, Anna Rita; Biunno, Ida; Bonelli, Raphael; Burgunder, Jean-Marc; Dunnett, Stephen; Ferreira, Joaquim; Handley, Olivia; Heiberg, Arvid; Illmann, Torsten; Landwehrmeyer, G. Bernhard; Levey, Jamie; Ramos-Arroyo, Maria A.; Nielsen, Jã¸rgen; Koivisto, Susana Pro; Pã¤ivã¤rinta, Markku; Roos, Raymund A. C.; Sebastiã¡n, A. Rojo; Tabrizi, Sarah; Vandenberghe, Wim; Verellen-Dumoulin, Christine; Uhrova, Tereza; Wahlstrã¶m, Jan; Zaremba, Jacek; Baake, Verena; Barth, Katrin; Garde, Monica Bascuñana; Betz, Sabrina; Bos, Reineke; Callaghan, Jenny; Come, Adrien; Guedes, Leonor Correia; Ecker, Daniel; Finisterra, Ana Maria; Fullam, Ruth; Gilling, Mette; Gustafsson, Lena; Handley, Olivia J; Hvalstedt, Carina; Held, Christine; Koppers, Kerstin; Lamanna, Claudia; Laurã , Matilde; Descals, Asunción Martínez; Martinez-Horta, Saã¼l; Mestre, Tiago; Minster, Sara; Monza, Daniela; Mã¼tze, Lisanne; Oehmen, Martin; Orth, Michael; Padieu, Hã©lãne; Paterski, Laurent; Peppa, Nadia; Koivisto, Susana Pro; Di Renzo, Martina; Rialland, Amandine; Rã¸ren, Niini; Å aå¡inkovã¡, Pavla; Timewell, Erika; Townhill, Jenny; Cubillo, Patricia Trigo; da Silva, Wildson Vieira; van Walsem, Marleen R; Whalstedt, Carina; Witjes-Ané, Marie-Noelle; Witkowski, Grzegorz; Wright, Abigail; Zielonka, Daniel; Zielonka, Eugeniusz; Zinzi, Paola; Bonelli, Raphael M.; Lilek, Sabine; Hecht, Karen; Herranhof, Brigitte; Holl, Anna; Kapfhammer, Hans-Peter; Koppitz, Michael; Magnet, Markus; Mã¼ller, Nicole; Otti, Daniela; Painold, Annamaria; Reisinger, Karin; Scheibl, Monika; Schã¶ggl, Helmut; Ullah, Jasmin; Braunwarth, Eva-Maria; Brugger, Florian; Buratti, Lisa; Hametner, Eva-Maria; Hepperger, Caroline; Holas, Christiane; Hotter, Anna; Hussl, Anna; Mã¼ller, Christoph; Poewe, Werner; Seppi, Klaus; Sprenger, Fabienne; Wenning, Gregor; Boogaerts, Andrea; Calmeyn, Godelinde; Delvaux, Isabelle; Liessens, Dirk; Somers, Nele; Dupuit, Michel; Minet, Cã©cile; van Paemel, Dominique; Ribaã¯, Pascale; Verellen-Dumoulin, Christine; Boogaerts, Andrea; Vandenberghe, Wim; van Reijen, Dimphna; Klempã­r, Jirã­; Majerovã¡, Veronika; Roth, Jan; Stã¡rkovã¡, Irena; Hjermind, Lena E.; Jacobsen, Oda; Nielsen, Jørgen E.; Larsen, Ida Unmack; Vinther-Jensen, Tua; Hiivola, Heli; Hyppã¶nen, Hannele; Martikainen, Kirsti; Tuuha, Katri; Allain, Philippe; Bonneau, Dominique; Bost, Marie; Gohier, Bã©nã©dicte; Guã©rid, Marie-Anne; Olivier, Audrey; Prundean, Adriana; Scherer-Gagou, Clarisse; Verny, Christophe; Babiloni, Blandine; Debruxelles, Sabrina; Duchã©, Charlotte; Goizet, Cyril; Jameau, Laetitia; Lafoucriãre, Danielle; Spampinato, Umberto; Barthã©lã©my, Rekha; De Bruycker, Christelle; Carette, Maryline Cabaret Anne-Sophie; Defebvre, Eric Decorte Luc; Delliaux, Marie; Delval, Arnaud; Destee, Alain; Dujardin, Kathy; Lemaire,, Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study, «LANCET NEUROLOGY», 2017, 16, pp. 701 - 711 [articolo]

Giannoccaro, Maria Pia; Bartoletti-Stella, Anna; Piras, Silvia; Pession, Annalisa; De Massis, Patrizia; Oppi, Federico; Stanzani-Maserati, Michelangelo; Pasini, Elena; Baiardi, Simone; Avoni, Patrizia; Parchi, Piero; Liguori, Rocco; Capellari, Sabina, Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature, «JOURNAL OF NEUROLOGY», 2017, 264, pp. 1426 - 1433 [articolo]

Terlizzi, Rossana; Valentino, Maria Lucia; Bartoletti-Stella, Anna; Columbaro, Marta; Piras, Silvia; Stanzani-Maserati, Michelangelo; Quadri, Marialuisa; Breedveld, Guido J.; Bonifati, Vincenzo; Martinelli, Paolo; Parchi, Piero; Capellari, Sabina, Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation, «MOVEMENT DISORDERS», 2017, 32, pp. 1259 - 1260 [articolo]

Vita, Maria Gabriella; Tiple, Dorina; Bizzarro, Alessandra; Ladogana, Anna; Colaizzo, Elisa; Capellari, Sabina; Rossi, Marcello; Parchi, Piero; Masullo, Carlo; Pocchiari, Maurizio, Patient with rapidly evolving neurological disease with neuropathological lesions of Creutzfeldt-Jakob disease, Lewy body dementia, chronic subcortical vascular encephalopathy and meningothelial meningioma, «NEUROPATHOLOGY», 2017, 37, pp. 110 - 115 [articolo]

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 [articolo]Open Access

Donadio, Vincenzo; Incensi, Alex; Rizzo, Giovanni; Scaglione, Cesa; Capellari, Sabina; Fileccia, Enrico; Avoni, Patrizia; Liguori, Rocco, Spine Topographical Distribution of Skin α-Synuclein Deposits in Idiopathic Parkinson Disease, «JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY», 2017, 76, pp. 384 - 389 [articolo]

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 [articolo]

Sailer, Anna; Scholz, Sonja W; Nalls, Michael A; Schulte, Claudia; Federoff, Monica; Price, T Ryan; Lees, Andrew; Ross, Owen A; Dickson, Dennis W; Mok, Kin; Mencacci, Niccolo E; Schottlaender, Lucia; Chelban, Viorica; Ling, Helen; O'Sullivan, Sean S; Wood, Nicholas W; Traynor, Bryan J; Ferrucci, Luigi; Federoff, Howard J; Mhyre, Timothy R; Morris, Huw R; Deuschl, Günther; Quinn, Niall; Widner, Hakan; Albanese, Alberto; Infante, Jon; Bhatia, Kailash P; Poewe, Werner; Oertel, Wolfgang; Höglinger, Günter U; Wüllner, Ullrich; Goldwurm, Stefano; Pellecchia, Maria Teresa; Ferreira, Joaquim; Tolosa, Eduardo; Bloem, Bastiaan R; Rascol, Olivier; Meissner, Wassilios G; Hardy, John A; Revesz, Tamas; Holton, Janice L; Gasser, Thomas; Wenning, Gregor K; Singleton, Andrew B; Houlden, Henry; European Multiple System Atrophy Study Group [; Giovanna, Calandra Buonaura; Sabina, Capellari; Pietro, Cortelli;] and the UK Multiple System Atrophy Study Group, A genome-wide association study in multiple system atrophy, «NEUROLOGY», 2016, 87, pp. 1591 - 1598 [articolo]

Terlizzi, Rossana; Calandra-Buonaura, Giovanna; Zanigni, Stefano; Barletta, Giorgio; Capellari, Sabina; Guaraldi, Pietro; Donadio, Vincenzo; Cason, Ernesto; Contin, Manuela; Poda, Roberto; Tonon, Caterina; Sambati, Luisa; Gallassi, Roberto; Liguori, Rocco; Lodi, Raffaele; Cortelli, Pietro, A longitudinal study of a family with adult-onset autosomal dominant leukodystrophy: Clinical, autonomic and neuropsychological findings, «AUTONOMIC NEUROSCIENCE: BASIC & CLINICAL», 2016, 195, pp. 20 - 26 [articolo]

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 [articolo]

Rizzo, Giovanni; Licchetta, Laura; Scaglione, Cesa; Buttiglione, Maura; Capellari, Sabina; Martinelli, Paolo; Martino, Davide, Behçet disease presenting with movement disorders and antibasal ganglia antibodies, «AUTOIMMUNITY REVIEWS», 2016, 15, pp. 287 - 288 [replica/breve intervento]

CALANDRA BUONAURA, Giovanna; Doria, Andrea; Lopane, Giovanna; Guaraldi, Pietro; Capellari, Sabina; Martinelli, Paolo; Cortelli, Pietro; Contin, MANUELA MARIA ANTONIA, Pharmacodynamics of a low subacute levodopa dose helps distinguish between multiple system atrophy with predominant Parkinsonism and Parkinson’s disease, «JOURNAL OF NEUROLOGY», 2016, 263, pp. 250 - 256 [articolo]