DE STEFANO, NICOLA
DE STEFANO, NICOLA
Dipartimento di Scienze Mediche, Chirurgiche e Neuroscienze
1H-MR Spectroscopy in Traumatic Brain Injury
2011-01-01 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
2021-01-01 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
2017-01-01 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
2008-01-01 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
2023-01-01 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
2014-01-01 Hakiki, B.; Niccolai, C.; Portaccio, E.; Goretti, B.; Giannini, M.; Pastò, L.; Pecori, C .; Stromillo, M. L.; Giorgio, A.; Rossi, F.; De Stefano, N.; Amato, M. P.
A Deep Learning Approach to Predicting Disease Progression in Multiple Sclerosis Using Magnetic Resonance Imaging
2022-01-01 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
2022-01-01 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
2015-01-01 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
2011-01-01 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.
2005-01-01 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.
2006-01-01 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
2014-01-01 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
2001-01-01 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
2004-01-01 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
2016-01-01 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
1997-01-01 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
2002-01-01 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
2016-01-01 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
2009-01-01 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.
| 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.; Pastò, L.; Pecori, C .; Stromillo, M. L.; Giorgio, A.; Rossi, F.; De Stefano, N.; Amato, M. P. | - | |
| 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. | - |