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Page 1
Patient-Relevant Digital-Motor Outcomes for Clinical Trials in Hereditary Spastic Paraplegia Type 7: A Multicenter PROSPAX Study.
Beichert L, Seemann J, Kessler C, Traschütz A, Müller D, Dillmann-Jehn K, Ricca I, Satolli S, Basak NA, Coarelli G, Timmann D, Gagnon C, van de Warrenburg BPC; PROSPAX Consortium; Ilg W, Synofzik M, Schüle R. Beichert L, et al. Among authors: satolli s. Neurology. 2024 Dec 24;103(12):e209887. doi: 10.1212/WNL.0000000000209887. Epub 2024 Dec 2. Neurology. 2024. PMID: 39621946 Free PMC article.
Psychometric properties and clinical correlates of the Frontal Behaviour Inventory in progressive supranuclear palsy: data from the PSP-NET.
Cappiello A, Cuoco S, De Micco R, Satolli S, Di Biasio F, Markushi TB, Sambati L, Pilotto A, Costanzo M, Longo C, Schirinzi T, Del Prete E, Frosini D, Stefani A, Malaguti MC, Fabbrini G, Padovani A, Calandra-Buonaura G, Marchese R, Tessitore A, Barone P, Picillo M; P. S. P.-N. E. T. study group. Cappiello A, et al. Among authors: satolli s. Neurol Sci. 2024 Nov 23. doi: 10.1007/s10072-024-07887-w. Online ahead of print. Neurol Sci. 2024. PMID: 39579261
Correction to: Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia-experience from an Italian cohort.
Satolli S, Rossi S, Vegezzi E, Pellerin D, Manca ML, Barghigiani M, Battisti C, Bilancieri G, Bruno G, Capacci E, Casali C, Ceravolo R, Cocozza S, Cotti Piccinelli S, Criscuolo C, Danzi MC, De Micco R, De Michele G, Dicaire MJ, Falcone GMI, Fancellu R, Ferchichi Y, Ferrari C, Filla A, Fini N, Govoni A, Lo Vecchio F, Malandrini A, Mignarri A, Musumeci O, Nesti C, Pappatà S, Pellecchia MT, Perna A, Petrucci A, Pomponi MG, Ravenni R, Ricca I, Rufa A, Tabolacci E, Tessa A, Tessitore A, Zuchner S, Silvestri G, Cortese A, Brais B, Santorelli FM. Satolli S, et al. J Neurol. 2024 Dec;271(12):7650-7651. doi: 10.1007/s00415-024-12629-1. J Neurol. 2024. PMID: 39499281 No abstract available.
Unveiling a new oceanic anoxic event at the Norian/Rhaetian boundary (Late Triassic).
Rigo M, Jin X, Godfrey L, Katz ME, Sato H, Tomimatsu Y, Zaffani M, Maron M, Satolli S, Concheri G, Cardinali A, Wu Q, Du Y, Lei JZX, van Wieren CS, Tackett LS, Campbell H, Bertinelli A, Onoue T. Rigo M, et al. Among authors: satolli s. Sci Rep. 2024 Jul 6;14(1):15574. doi: 10.1038/s41598-024-66343-z. Sci Rep. 2024. PMID: 38971867 Free PMC article.
Multidisciplinary care use in neurodegenerative complex diseases: The example of progressive supranuclear palsy and advanced Parkinson's disease in real-life.
Fabbri M, Ledda C, Schirinzi T, Artusi CA, Avallone AR, Zenuni H, De Micco R, Aloisio S, Cani I, Malaguti MC, Di Biasio F, Calandra-Buonaura G, Stefani A, Lopiano L, Barone P, Picillo M; PSP-NET study group. Fabbri M, et al. Parkinsonism Relat Disord. 2024 Aug;125:107047. doi: 10.1016/j.parkreldis.2024.107047. Epub 2024 Jun 28. Parkinsonism Relat Disord. 2024. PMID: 38964017 Free article.
Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia-experience from an Italian cohort.
Satolli S, Rossi S, Vegezzi E, Pellerin D, Manca ML, Barghigiani M, Battisti C, Bilancieri G, Bruno G, Capacci E, Casali C, Ceravolo R, Cocozza S, Cotti Piccinelli S, Criscuolo C, Danzi MC, De Micco R, De Michele G, Dicaire MJ, Falcone GMI, Fancellu R, Ferchichi Y, Ferrari C, Filla A, Fini N, Govoni A, Lo Vecchio F, Malandrini A, Mignarri A, Musumeci O, Nesti C, Pappatà S, Pellecchia MT, Perna A, Petrucci A, Pomponi MG, Ravenni R, Ricca I, Rufa A, Tabolacci E, Tessa A, Tessitore A, Zuchner S, Silvestri G, Cortese A, Brais B, Santorelli FM. Satolli S, et al. J Neurol. 2024 Aug;271(8):5478-5488. doi: 10.1007/s00415-024-12506-x. Epub 2024 Jun 17. J Neurol. 2024. PMID: 38886208
MRI-ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX Study.
Scaravilli A, Negroni D, Senatore C, Ugga L, Cosottini M, Ricca I, Bender B, Traschütz A, Başak AN, Vural A, van de Warrenburg BP, Durr A, La Piana R, Timmann D; PROSPAX Consortium; Schüle R, Synofzik M, Santorelli FM, Cocozza S. Scaravilli A, et al. Mov Disord. 2024 Aug;39(8):1343-1351. doi: 10.1002/mds.29871. Epub 2024 Jun 7. Mov Disord. 2024. PMID: 38847051
SCAR32: Functional characterization and expansion of the clinical-genetic spectrum.
Naef V, Lieto M, Satolli S, De Micco R, Troisi M, Pasquariello R, Doccini S, Privitera F, Filla A, Tessitore A, Santorelli FM. Naef V, et al. Among authors: satolli s. Ann Clin Transl Neurol. 2024 Jul;11(7):1879-1886. doi: 10.1002/acn3.52094. Epub 2024 Jun 5. Ann Clin Transl Neurol. 2024. PMID: 38837640 Free PMC article.
18 results