Mammana A.; Baiardi S.; Quadalti C.; Rossi M.; Donadio V.; Capellari S.; Liguori R.; Parchi P., RT-QuIC Detection of Pathological α-Synuclein in Skin Punches of Patients with Lewy Body Disease, «MOVEMENT DISORDERS», 2021, 36, pp. 2173 - 2177 [Scientific article]Open Access
Bartoletti-Stella A.; Vacchiano V.; De Pasqua S.; Mengozzi G.; De Biase D.; Bartolomei I.; Avoni P.; Rizzo G.; Parchi P.; Donadio V.; Chio A.; Pession A.; Oppi F.; Salvi F.; Liguori R.; Capellari S., Targeted sequencing panels in Italian ALS patients support different etiologies in the ALS/FTD continuum, «JOURNAL OF NEUROLOGY», 2021, 268, pp. 3766 - 3776 [Scientific article]Open Access
Vacchiano V.; Mometto N.; Bartoletti-Stella A.; Rizzo G.; Abu-Rumeileh S.; Salvi F.; Parchi P.; Liguori R.; Capellari S., The clinical spectrum of multisystem proteinopathy: Data from a neurodegenerative cohort, «JOURNAL OF THE NEUROLOGICAL SCIENCES», 2021, 426, pp. 117478 - 117478 [Comment or similar]
Mitolo M.; Stanzani-Maserati M.; Manners D.N.; Capellari S.; Testa C.; Talozzi L.; Poda R.; Oppi F.; Evangelisti S.; Gramegna L.L.; Magarelli S.; Pantieri R.; Liguori R.; Lodi R.; Tonon C., The combination of metabolic posterior cingulate cortical abnormalities and structural asymmetries improves the differential diagnosis between primary progressive aphasia and alzheimer's disease, «JOURNAL OF ALZHEIMER'S DISEASE», 2021, 82, pp. 1467 - 1473 [Scientific article]
Areskeviciute A.; Lund E.L.; Capellari S.; Parchi P.; Pinkowsky C.T., The first sporadic creutzfeldt–jakob disease case with a rare molecular subtype vv1 and 1-octapeptide repeat deletion in prnp, «VIRUSES», 2021, 13, Article number: 2061 , pp. 1 - 7 [Scientific article]Open Access
Mantovani P.; Albini-Riccioli L.; Giannini G.; Milletti D.; Sorenson T.J.; Stanzani Maserati M.; Oppi F.; Elder B.D.; Cevoli S.; Cortelli P.; Palandri G.; Agati R.; Calandra Buonaura G.; Capellari S.; Chiari L.; Ferrari A.; Merola M.; Parchi P.; Pirina A.; Piserchia V.A.; Ricci V.; Sambati L.; Sturiale C.; Supino A., Anterior Callosal Angle: A New Marker of Idiopathic Normal Pressure Hydrocephalus?, «WORLD NEUROSURGERY», 2020, 139, pp. e548 - e552 [Scientific article]
Martina Tarozzi, Anna Bartoletti-Stella, Daniele Dall'Olio, Tommaso Matteuzzi, Sabina Capellari, Gastone Castellani, Binary transformation of sequencing data to explore functional genetic patterns., in: Binary transformation of sequencing data to explore functional genetic patterns., 2020(atti di: EMBL PhD symposium 2020, Virtuale, 27-28/11/2020) [Poster]
Romagnoli M.; Stanzani Maserati M.; De Matteis M.; Capellari S.; Carbonelli M.; Amore G.; Cantalupo G.; Zenesini C.; Liguori R.; Sadun A.A.; Carelli V.; Park J.C.; La Morgia C., Chromatic Pupillometry Findings in Alzheimer’s Disease, «FRONTIERS IN NEUROSCIENCE», 2020, 14, Article number: 780 , pp. 780 - 780 [Scientific article]Open Access
Abu-Rumeileh S.; Baiardi S.; Ladogana A.; Zenesini C.; Bartoletti-Stella A.; Poleggi A.; Mammana A.; Polischi B.; Pocchiari M.; Capellari S.; Parchi P., Comparison between plasma and cerebrospinal fluid biomarkers for the early diagnosis and association with survival in prion disease, «JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY», 2020, 91, pp. 1181 - 1188 [Scientific article]
Abu-Rumeileh S.; Steinacker P.; Polischi B.; Mammana A.; Bartoletti-Stella A.; Oeckl P.; Baiardi S.; Zenesini C.; Huss A.; Cortelli P.; Capellari S.; Otto M.; Parchi P., CSF biomarkers of neuroinflammation in distinct forms and subtypes of neurodegenerative dementia, «ALZHEIMER'S RESEARCH & THERAPY», 2020, 12, Article number: 2 , pp. 2 - 2 [Scientific article]Open Access
Abu-Rumeileh S.; Halbgebauer S.; Steinacker P.; Anderl-Straub S.; Polischi B.; Ludolph A.C.; Capellari S.; Parchi P.; Otto M., CSF SerpinA1 in Creutzfeldt–Jakob disease and frontotemporal lobar degeneration, «ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY», 2020, 7, pp. 191 - 199 [Scientific article]Open Access
Abu-Rumeileh S.; Oeckl P.; Baiardi S.; Halbgebauer S.; Steinacker P.; Capellari S.; Otto M.; Parchi P., Csf ubiquitin levels are higher in alzheimer’s disease than in frontotemporal dementia and reflect the molecular subtype in prion disease, «BIOMOLECULES», 2020, 10, Article number: 497 , pp. 497 - 508 [Scientific article]Open Access
Mammana A.; Baiardi S.; Rossi M.; Franceschini A.; Donadio V.; Capellari S.; Caughey B.; Parchi P., Detection of prions in skin punch biopsies of Creutzfeldt–Jakob disease patients, «ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY», 2020, 7, pp. 559 - 564 [Scientific article]Open Access
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 [Scientific article]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 [Scientific article]
