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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]
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
Muccioli, Lorenzo; Mammana, Angela; Incensi, Alex; Baiardi, Simone; Parchi, Piero; Liguori, Rocco; Donadio, Vincenzo, The In Vivo Diagnosis of Concomitant Alzheimer and Lewy Body Pathology: A Case Report, «JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY», 2021, 80, pp. 1085 - 1087 [Comment or similar]
Baiardi, Simone; Pizza, Fabio; Polischi, Barbara; Moresco, Monica; Abu-Rumeileh, Samir; Plazzi, Giuseppe; Parchi, Piero, Cerebrospinal fluid biomarkers of neurodegeneration in narcolepsy type 1, «SLEEP», 2020, 43, Article number: zsz215 , pp. 1 - 5 [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]
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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 [Scientific article]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 [Scientific article]
