DE STEFANO, NICOLA

DE STEFANO, NICOLA  

Dipartimento di Scienze Mediche, Chirurgiche e Neuroscienze  

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Titolo Data di pubblicazione Autore(i) File Abstract
1H-MR Spectroscopy in Traumatic Brain Injury 1-gen-2011 Marino, S; Ciurleo, R; Bramanti, P; Federico, Antonio; DE STEFANO, Nicola -
2021 MAGNIMS-CMSC-NAIMS consensus recommendations on the use of MRI in patients with multiple sclerosis 1-gen-2021 Wattjes, Mike P; Ciccarelli, Olga; Reich, Daniel S; Banwell, Brenda; de Stefano, Nicola; Enzinger, Christian; Fazekas, Franz; Filippi, Massimo; Frederiksen, Jette; Gasperini, Claudio; Hacohen, Yael; Kappos, Ludwig; Li, David K B; Mankad, Kshitij; Montalban, Xavier; Newsome, Scott D; Oh, Jiwon; Palace, Jacqueline; Rocca, Maria A; Sastre-Garriga, Jaume; Tintoré, Mar; Traboulsee, Anthony; Vrenken, Hugo; Yousry, Tarek; Barkhof, Frederik; Rovira, Àlex -
[(11)C]PBR28 or [(18)F]PBR111 detect white matter inflammatory heterogeneity in multiple sclerosis 1-gen-2017 Datta, Gourab; Colasanti, Alessandro; Kalk, Nicola; Owen, David R; Scott, Gregory; Rabiner, Eugenii Ilan A; Gunn, Roger; Lingford Hughes, Anne; Malik, Omar; Ciccarelli, Olga; Nicholas, Richard; Nie, Lei; Battaglini, Marco; DE STEFANO, Nicola; Matthews, Paul -
A case of ovarioleukodystrophy without elF2B mutations 1-gen-2008 Gaudiano, C.; Di PerriI, C.; Scali, O.; Rufa, Alessandra; Battisti, Carla; De Stefano, Nicola; Federico, Antonio -
A case report of FAVA syndrome in a young woman carrying a mutation in the PIK3CA gene 1-gen-2023 Costagliola, Antonella; Arcuri, Felice; Pelliccioni, Pietro; Malandrini, Alessandro; De Stefano, Nicola; Battisti, Carla -
A comparison of cognitive performances between multiple sclerosis patients with pediatric- versus adult onset disease 1-gen-2014 Hakiki, B.; Niccolai, C.; Portaccio, E.; Goretti, B.; Giannini, M.; Pasto’, L.; Pecori, C.; Stromillo, Ml; Giorgio, Antonio; Rossi, F.; De Stefano, N.; Amato, Mp -
A Deep Learning Approach to Predicting Disease Progression in Multiple Sclerosis Using Magnetic Resonance Imaging 1-gen-2022 Storelli, Loredana; Azzimonti, Matteo; Gueye, Mor; Vizzino, Carmen; Preziosa, Paolo; Tedeschi, Gioachino; De Stefano, Nicola; Pantano, Patrizia; Filippi, Massimo; Rocca, Maria A -
A double-blind, randomized, placebo-controlled phase 2 trial evaluating the selective dihydroorotate dehydrogenase inhibitor vidofludimus calcium in relapsing-remitting multiple sclerosis 1-gen-2022 Fox, Robert J; Wiendl, Heinz; Wolf, Christian; De Stefano, Nicola; Sellner, Johann; Gryb, Viktoriia; Rejdak, Konrad; Bozhinov, Plamen Stoyanov; Tomakh, Nataliya; Skrypchenko, Iryna; Muehler, Andreas R -
A human post-mortem brain model for the standardization of multi-centre MRI studies 1-gen-2015 Droby, Amgad; Lukas, Carsten; Schänzer, Anne; Spiwoks Becker, Isabella; Giorgio, Antonio; Gold, Ralf; DE STEFANO, Nicola; Kugel, Harald; Deppe, Michael; Wiendl, Heinz; Meuth, Sven G.; Acker, Till; Zipp, Frauke; Deichmann, Ralf -
A multicentre study of motor functional connectivity changes in patients with multiple sclerosis 1-gen-2011 Valsasina, P; Rocca, Ma; Absinta, M; Sormani, Mp; Mancini, L; DE STEFANO, Nicola; Rovira, A; Gass, A; Enzinger, C; Barkhof, F; Wegner, C; Matthews, Pm; Filippi, M. -
A new family with CADASIL: presentation of an homozygous patient and comparison with heterozigous phenotypes. 1-gen-2005 Sperduto, A; Dotti, Maria; DE STEFANO, Nicola; De Santis, M; Bianchi, Silvia; Rufa, Alessandra; Frantellizzi, P; Federico, Antonio -
A new missense mutation in caveolin-3 gene causes rippling muscle disease. 1-gen-2006 Dotti, Maria; Malandrini, Alessandro; Gambelli, Simona; Salvadori, Claudio; DE STEFANO, Nicola; Federico, Antonio -
A novel approach with “skeletonised MTR” measures tract-specific microstructural changes in early primary-progressive MS 1-gen-2014 Benedetta, Bodini; Mara, Cercignani; Ahmed, Toosy; DE STEFANO, Nicola; David H., Miller; Alan J., Thompson; Olga, Ciccarelli -
A Novel Mutation in the Notch3 Gene in an Italian Family with CADASIL: Genetic and MRI Spectroscopic Findings 1-gen-2001 Oliveri, R. L.; Muglia, M.; DE STEFANO, N.; Mazzei, R.; Labate, A.; Conforti, F. L.; Patitucci, A.; Gabriele, A. L.; Magariello, A.; Zappia, M.; Gambardella, A.; Federico, A.; Quattrone, A. -
A novel NOTCH3 frameshift deletion and mitochondrial abnormalities in a patient with CADASIL 1-gen-2004 Dotti, M. T.; DE STEFANO, N.; Bianchi, S.; Malandrini, A.; Battisti, C.; Cardaioli, E.; Federico, A. -
A practical review of the neuropathology and neuroimaging of multiple sclerosis 1-gen-2016 Matthews, Paul M; Roncaroli, Frederico; Waldman, Adam; Sormani, Maria Pia; DE STEFANO, Nicola; Giovannoni, Gavin; Reynolds, Richard -
A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case 1-gen-1997 Plewnia, K; Dotti, Maria; Malandrini, Alessandro; Manneschi, L; Battisti, Carla; DE STEFANO, Nicola; Rufa, Alessandra; Motolese, Eduardo; Federico, Antonio -
A Rett syndrome MECP2 mutation that causes mental retardation in men 1-gen-2002 Dotti, Maria; Orrico, A.; DE STEFANO, Nicola; Battisti, Carla; Sicurelli, F.; Severi, S.; Lam, C. W.; Galli, L.; Sorrentino, Vincenzo; Federico, Antonio -
A semiautomatic method for multiple sclerosis lesion segmentation on Dual-Echo MR imaging: Application in a multicenter context 1-gen-2016 Storelli, L.; Pagani, E.; Rocca, M. A.; Horsfield, M. A.; Gallo, A.; Bisecco, A.; Battaglini, Marco; DE STEFANO, Nicola; Vrenken, H.; Thomas, D. L.; Mancini, L.; Ropele, S.; Enzinger, C.; Preziosa, P.; Filippi, M. -
Abnormal connectivity of the sensorimotor network in patients with MS: A multicenter fMRI study 1-gen-2009 Rocca, Ma; Absinta, M; Valsasina, P; Ciccarelli, O; Marino, S; Rovira, A; Gass, A; Wegner, C; Enzinger, C; Korteweg, T; Sormani, Mp; Mancini, L; Thompson, Aj; DE STEFANO, Nicola; Montalban, X; Hirsch, J; Kappos, L; Ropele, S; Palace, J; Barkhof, F; Matthews, Pm; Filippi, M. -