Testa, Claudia; Evangelisti, Stefania; Popeo, Mariagrazia; Zanigni, Stefano; Gramegna, Laura Ludovica; Fantazzini, Paola; Tonon, Caterina; Manners, David Neil; Lodi, Raffaele, The effect of diffusion gradient direction number on corticospinal tractography in the human brain: an along-tract analysis, «MAGNETIC RESONANCE MATERIALS IN PHYSICS BIOLOGY AND MEDICINE», 2017, 30, pp. 265 - 280 [Scientific article]
Zanigni, S; Evangelisti, S; Testa, C; Manners, Dn; Calandra-Buonaura, G; Guarino, M; Gabellini, A; Gramegna, Ll; Giannini, G; Sambati, L; Cortelli, P; Lodi, R; Tonon, C., White matter and cortical changes in atypical parkinsonisms: A multimodal quantitative MR study, «PARKINSONISM & RELATED DISORDERS», 2017, 39, pp. 44 - 51 [Scientific article]
Terlizzi, Rossana; Calandra-Buonaura, Giovanna; Zanigni, Stefano; Barletta, Giorgio; Capellari, Sabina; Guaraldi, Pietro; Donadio, Vincenzo; Cason, Ernesto; Contin, Manuela; Poda, Roberto; Tonon, Caterina; Sambati, Luisa; Gallassi, Roberto; Liguori, Rocco; Lodi, Raffaele; Cortelli, Pietro, A longitudinal study of a family with adult-onset autosomal dominant leukodystrophy: Clinical, autonomic and neuropsychological findings, «AUTONOMIC NEUROSCIENCE: BASIC & CLINICAL», 2016, 195, pp. 20 - 26 [Scientific article]
Zanigni, Stefano; Calandra-Buonaura, Giovanna; Manners, David Neil; Testa, Claudia; Gibertoni, Dino; Evangelisti, Stefania; Sambati, Luisa; Guarino, Maria; De Massis, Patrizia; Gramegna, Laura Ludovica; Bianchini, Claudio; Rucci, Paola; Cortelli, Pietro; Lodi, Raffaele; Tonon, Caterina, Accuracy of MR markers for differentiating Progressive Supranuclear Palsy from Parkinson's disease, «NEUROIMAGE. CLINICAL», 2016, 11, pp. 736 - 742 [Scientific article]Open Access
D'Angelo, R; Rinaldi, R; Carelli, V; Boschetti, E; Caporali, L; Capristo, M; Casali, C; Cenacchi, G; Gramegna, Ll; Lodi, R; Pinna, Ad; Pironi, L; Stanzani, M; Tonon, C; D'Alessandro, R; De Giorgio, R, ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathy., «NEUROLOGICAL SCIENCES», 2016, 37, pp. 1149 - 1151 [Scientific article]
De Giorgio, Roberto; Pironi, Loris; Rinaldi, Rita; Boschetti, Elisa; Caporali, Leonardo; Capristo, Mariantonietta; Casali, Carlo; Cenacchi, Giovanna; Contin, Manuela; D'Angelo, Roberto; D'Errico, Antonietta; Gramegna, Laura Ludovica; Lodi, Raffaele; Maresca, Alessandra; Mohamed, Susan; Morelli, Maria Cristina; Papa, Valentina; Tonon, Caterina; Tugnoli, Vitaliano; Carelli, Valerio; D'Alessandro, Roberto; Pinna, Antonio Daniele, Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy, «ANNALS OF NEUROLOGY», 2016, 80, pp. 448-55 - 455 [Scientific article]Open Access
Testa, Claudia; Pultrone, CRISTIAN VINCENZO; Manners, DAVID NEIL; Schiavina, Riccardo; Lodi, Raffaele, Metabolic Imaging in Prostate Cancer: Where We Are, «FRONTIERS IN ONCOLOGY», 2016, 6, Article number: 225 , pp. 1 - 8 [Scientific article]Open Access
Zanigni, Stefano; Evangelisti, Stefania; Giannoccaro, Maria Pia; Oppi, Federico; Poda, Roberto; Giorgio, Antonio; Testa, Claudia; Manners, David Neil; Avoni, Patrizia; Gramegna, Laura Ludovica; De Stefano, Nicola; Lodi, Raffaele; Tonon, Caterina; Liguori, Rocco, Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1, «NEUROIMAGE. CLINICAL», 2016, 11, pp. 678 - 685 [Scientific article]Open Access
Nicoletti, Giuseppe; Manners, David Neil; Novellino, Fabiana; Testa, Claudia; Gagliardi, Monica; Tonon, Caterina; Lodi, Raffaele; Quattrone, Aldo, Voxel-based morphometry to detect effect of APOE on brain gray matter changes in Parkinson's Disease, «PSYCHIATRY RESEARCH. NEUROIMAGING», 2016, 254, pp. 177 - 179 [Scientific article]
Carelli, Valerio; Sabatelli, Mario; Carrozzo, Rosalba; Rizza, Teresa; Schimpf, Simone; Wissinger, Bernd; Zanna, Claudia; Rugolo, Michela; La Morgia, Chiara; Caporali, Leonardo; Carbonelli, Michele; Barboni, Piero; Tonon, Caterina; Lodi, Raffaele; Bertini, Enrico, 'Behr syndrome' with OPA1 compound heterozygote mutations, «BRAIN», 2015, 138, pp. e321 - e321 [Scientific article]
Morisi R, Gnecco G, Lanconelli N, Zanigni S, Manners DN, Testa C, Evangelisti S, Gramegna LL, Bianchini C, Cortelli P, Tonon C, Lodi, R, Binary and multi-class parkinsonian disorders classification using support vector machines, in: Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics), Springer Verlag, 2015, 9117, pp. 379 - 386 (atti di: th Iberian Conference on Pattern Recognition and Image Analysis, IbPRIA 2015, Santiago de Compostela; Spain, 17-19 June 2015) [Contribution to conference proceedings]
Zanigni, Stefano; Terlizzi, Rossana; Tonon, Caterina; Testa, Claudia; Manners, David Neil; Capellari, Sabina; Gallassi, Roberto; Poda, Roberto; Gramegna, Laura Ludovica; Calandra-Buonaura, Giovanna; Sambati, Luisa; Cortelli, Pietro; Lodi, Raffaele, Brain magnetic resonance metabolic and microstructural changes in adult-onset autosomal dominant leukodystrophy, «BRAIN RESEARCH BULLETIN», 2015, 117, pp. 24 - 31 [Scientific article]
Manners, D.N.; Rizzo, G.; La Morgia, C.; Tonon, C.; Testa, C.; Barboni, P.; Malucelli, E.; Valentino, M.L.; Caporali, L.; Strobbe, D.; Carelli, V.; Lodi, R., Diffusion tensor imaging mapping of brain white matter pathology in mitochondrial optic neuropathies, «AJNR, AMERICAN JOURNAL OF NEURORADIOLOGY», 2015, 36, pp. 1259 - 1265 [Scientific article]
T. Pippucci;A. Maresca;P. Magini;G. Cenacchi;V. Donadio;F. Palombo;V. Papa;A. Incensi;G. Gasparre;M. L. Valentino;C. Preziuso;A. Pisano;M. Ragno;R. Liguori;C. Giordano;C. Tonon;R. Lodi;A. Parmeggiani;V. Carelli;M. Seri, Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy, «EMBO MOLECULAR MEDICINE», 2015, 7, pp. 848 - 858 [Scientific article]Open Access
Abrams, A.J.; Hufnagel, R.B.; Rebelo, A.; Zanna, C.; Patel, N.; Gonzalez, M.A.; Campeanu, I.J.; Griffin, L.B.; Groenewald, S.; Strickland, A.V.; Tao, F.; Speziani, F.; Abreu, L.; Schule, R.; Caporali, L.; La Morgia, C.; Maresca, A.; Liguori, R.; Lodi, R.; Ahmed, Z.M.; Sund, K.L.; Wang, X.; Krueger, L.A.; Peng, Y.; Prada, C.E.; Prows, C.A.; Schorry, E.K.; Antonellis, A.; Zimmerman, H.H.; Abdul-Rahman, O.A.; Yang, Y.; Downes, S.M.; Prince, J.; Fontanesi, F.; Barrientos, A.; Nemeth, A.H.; Carelli, V.; Huang, T.; Zuchner, S.; Dallman, J.E., Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder, «NATURE GENETICS», 2015, 47, pp. 926 - 932 [Scientific article]Open Access
