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Baiardi S.; Mammana A.; Rossi M.; Ladogana A.; Carla B.; Gambetti P.; Capellari S.; Parchi P., Phenotypic Heterogeneity of Variably Protease-Sensitive Prionopathy: A Report of Three Cases Carrying Different Genotypes at PRNP Codon 129, «VIRUSES», 2022, 14, Article number: 367, pp. 367 - 379 [articolo]Open Access
Jansen W.J.; Janssen O.; Tijms B.M.; Vos S.J.B.; Ossenkoppele R.; Visser P.J.; Aarsland D.; Alcolea D.; Altomare D.; Von Arnim C.; Baiardi S.; Baldeiras I.; Barthel H.; Bateman R.J.; Van Berckel B.; Binette A.P.; Blennow K.; Boada M.; Boecker H.; Bottlaender M.; Den Braber A.; Brooks D.J.; Van Buchem M.A.; Camus V.; Carill J.M.; Cerman J.; Chen K.; Chetelat G.; Chipi E.; Cohen A.D.; Daniels A.; Delarue M.; Didic M.; Drzezga A.; Dubois B.; Eckerstrom M.; Ekblad L.L.; Engelborghs S.; Epelbaum S.; Fagan A.M.; Fan Y.; Fladby T.; Fleisher A.S.; Van Der Flier W.M.; Forster S.; Fortea J.; Frederiksen K.S.; Freund-Levi Y.; Frings L.; Frisoni G.B.; Frohlich L.; Gabryelewicz T.; Gertz H.-J.; Gill K.D.; Gkatzima O.; Gomez-Tortosa E.; Grimmer T.; Guedj E.; Habeck C.G.; Hampel H.; Handels R.; Hansson O.; Hausner L.; Hellwig S.; Heneka M.T.; Herukka S.-K.; Hildebrandt H.; Hodges J.; Hort J.; Huang C.-C.; Iriondo A.J.; Itoh Y.; Ivanoiu A.; Jagust W.J.; Jessen F.; Johannsen P.; Johnson K.A.; Kandimal, Prevalence Estimates of Amyloid Abnormality Across the Alzheimer Disease Clinical Spectrum, «JAMA NEUROLOGY», 2022, 79, pp. 228 - 243 [articolo]
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Gelpi E.; Baiardi S.; Nos C.; Dellavalle S.; Aldecoa I.; Ruiz-Garcia R.; Ispierto L.; Escudero D.; Casado V.; Barranco E.; Boltes A.; Molina-Porcel L.; Bargallo N.; Rossi M.; Mammana A.; Tiple D.; Vaianella L.; Stoegmann E.; Simonitsch-Klupp I.; Kasprian G.; Klotz S.; Hoftberger R.; Budka H.; Kovacs G.G.; Ferrer I.; Capellari S.; Sanchez-Valle R.; Parchi P., Sporadic Creutzfeldt-Jakob disease VM1: phenotypic and molecular characterization of a novel subtype of human prion disease, «ACTA NEUROPATHOLOGICA COMMUNICATIONS», 2022, 10, Article number: 114, pp. 1 - 12 [articolo]Open Access
Poleggi A.; Baiardi S.; Ladogana A.; Parchi P., The Use of Real-Time Quaking-Induced Conversion for the Diagnosis of Human Prion Diseases, «FRONTIERS IN AGING NEUROSCIENCE», 2022, 14, Article number: 874734, pp. 1 - 18 [articolo]Open Access
Watson N.; Hermann P.; Ladogana A.; Denouel A.; Baiardi S.; Colaizzo E.; Giaccone G.; Glatzel M.; Green A.J.E.; Haik S.; Imperiale D.; Mackenzie J.; Moda F.; Smith C.; Summers D.; Tiple D.; Vaianella L.; Zanusso G.; Pocchiari M.; Zerr I.; Parchi P.; Brandel J.-P.; Pal S., Validation of Revised International Creutzfeldt-Jakob Disease Surveillance Network Diagnostic Criteria for Sporadic Creutzfeldt-Jakob Disease, «JAMA NETWORK OPEN», 2022, 5, Article number: e2145878, pp. e2146319 - e2146330 [articolo]Open Access
Brockmann K.; Quadalti C.; Lerche S.; Rossi M.; Wurster I.; Baiardi S.; Roeben B.; Mammana A.; Zimmermann M.; Hauser A.-K.; Deuschle C.; Schulte C.; Waniek K.; Lachmann I.; Sjodin S.; Brinkmalm A.; Blennow K.; Zetterberg H.; Gasser T.; Parchi P., Association between CSF alpha-synuclein seeding activity and genetic status in Parkinson’s disease and dementia with Lewy bodies, «ACTA NEUROPATHOLOGICA COMMUNICATIONS», 2021, 9, Article number: 175, pp. 175 - 186 [articolo]Open Access
Hermann P.; Appleby B.; Brandel J.-P.; Caughey B.; Collins S.; Geschwind M.D.; Green A.; Haik S.; Kovacs G.G.; Ladogana A.; Llorens F.; Mead S.; Nishida N.; Pal S.; Parchi P.; Pocchiari M.; Satoh K.; Zanusso G.; Zerr I., Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease, «LANCET NEUROLOGY», 2021, 20, pp. 235 - 246 [articolo]Open Access
Hermann P.; Appleby B.; Brandel J.-P.; Caughey B.; Collins S.; Geschwind M.D.; Green A.; Haik S.; Kovacs G.G.; Ladogana A.; Llorens F.; Mead S.; Nishida N.; Pal S.; Parchi P.; Pocchiari M.; Satoh K.; Zanusso G.; Zerr I., Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease, «LANCET NEUROLOGY», 2021, 20, pp. 235 - 246 [articolo]
Abu-Rumeileh S.; Parchi P., Cerebrospinal Fluid and Blood Neurofilament Light Chain Protein in Prion Disease and Other Rapidly Progressive Dementias: Current State of the Art, «FRONTIERS IN NEUROSCIENCE», 2021, 15, Article number: 648743, pp. 1 - 9 [articolo]Open Access
Bartoletti-Stella A.; De Pasqua S.; Baiardi S.; Bartolomei I.; Mengozzi G.; Orio G.; Pastorelli F.; Piras S.; Poda R.; Raggi A.; Maserati M.S.; Tarozzi M.; Liguori R.; Salvi F.; Parchi P.; Capellari S., Characterization of novel progranulin gene variants in Italian patients with neurodegenerative diseases, «NEUROBIOLOGY OF AGING», 2021, 97, pp. 145.e7 - 145.e15 [articolo]
Rossi, M.; Baiardi, S.; Teunissen, C. E.; van de Beek, M.; Mammana, A.; Stanzani-Maserati, M.; Van der Flier, W. M.; Sambati, L.; Zenesini, C.; Caughey, B.; Capellari, S.; Lemstra, A. W.; Parchi, P.; Quadalti, C., Diagnostic Value of the CSF α-Synuclein Real-Time Quaking-Induced Conversion Assay at the Prodromal MCI Stage of Dementia With Lewy Bodies, «NEUROLOGY», 2021, 97, pp. e930 - e940 [articolo]Open Access
Mastrangelo, Andrea; Baiardi, Simone; Zenesini, Corrado; Poleggi, Anna; Mammana, Angela; Polischi, Barbara; Ladogana, Anna; Capellari, Sabina; Parchi, Piero, Diagnostic and prognostic performance of CSF α-synuclein in prion disease in the context of rapidly progressive dementia, «ALZHEIMER'S & DEMENTIA: DIAGNOSIS, ASSESSMENT & DISEASE MONITORING», 2021, 13, Article number: e12214, pp. 1 - 8 [articolo]Open Access
Sarapura-Castro E.; Cosentino C.; Landman J.; Landman A.; Torres L.; Nunez Y.; Capellari S.; Parchi P.; Cornejo-Olivas M., Early sensory disturbances and seizures are common manifestations of familial Creutzfeldt-Jakob disease due to E200K PRNP mutation: Case report from two Peruvian families, «CLINICAL NEUROLOGY AND NEUROSURGERY», 2021, 202, Article number: 106490, pp. 1 - 4 [articolo]
