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 [articolo]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 [articolo]
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 [articolo]
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) [Contributo in Atti di convegno]
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 [articolo]
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 [articolo]
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 [articolo]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 [articolo]Open Access
Carelli, V.; Musumeci, O.; Caporali, L.; Zanna, C.; La Morgia, C.; Del Dotto, V.; Porcelli, A.M.; Rugolo, M.; Valentino, M.L.; Iommarini, L.; Maresca, A.; Barboni, P.; Carbonelli, M.; Trombetta, C.; Valente, E.M.; Patergnani, S.; Giorgi, C.; Pinton, P.; Rizzo, G.; Tonon, C.; Lodi, R.; Avoni, P.; Liguori, R.; Baruzzi, A.; Toscano, A.; Zeviani, M., Syndromic parkinsonism and dementia associated with OPA1 missense mutations, «ANNALS OF NEUROLOGY», 2015, 78, pp. 21 - 38 [articolo]Open Access
Zanigni, S.; Testa, C.; Calandra-Buonaura, G.; Sambati, L.; Guarino, M.; Gabellini, A.; Evangelisti, S.; Cortelli, P.; Lodi, R.; Tonon, C., The contribution of cerebellar proton magnetic resonance spectroscopy in the differential diagnosis among parkinsonian syndromes, «PARKINSONISM & RELATED DISORDERS», 2015, 21, pp. 929 - 937 [articolo]
Carossa V;Ghelli A;Tropeano CV;Valentino ML;Iommarini L;Maresca A;Caporali L;Morgia CL;Liguori R;Barboni P;Carbonelli M;Rizzo G;Tonon C;Lodi R;Martinuzzi A;Nardo VD;Rugolo M;Ferretti L;Gandini F;Pala M;Achilli A;Olivieri A;Torroni A;Carelli V, A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance., «HUMAN MUTATION», 2014, 35, pp. 954 - 958 [articolo]
C. Tonon; L.L. Gramegna; D.N. Manners; C. Testa; C. Bianchini; R. Rinaldi; R. D'Angelo; R. Latorre; V. Stanghellini; R. De Giorgio; R. Lodi, Advanced brain MR study in mitochondrial neurogastrointestinal encephalomyopathy: double dissociation between severe CIPO, mild neurological, and severe neuroradiological findings, in: Special Issue: Abstracts of the 1st Federation Neurogastroenterology and Motility Scientific Meeting, September 5-7, 2014, Guangzhou, China, «NEUROGASTROENTEROLOGY & MOTILITY», 2014, 26, pp. 173 - 173 (atti di: 1st Federation Neurogastroenterology and Motility Scientific Meeting, Guangzhou, 5-7 september) [atti di convegno-poster]
C. La Morgia; L. Caporali; F. Gandini; A. Olivieri; F. Toni; S. Nassetti;
D. Brunetto; C. Stipa; C. Scaduto; A. Parmeggiani; C. Tonon; R. Lodi;
A. Torroni; V. Carelli, Association of the mtDNA m.4171C>A/MT-ND1 mutation with both optic neuropathy and bilateral brainstem lesions, «BMC NEUROLOGY», 2014, 14, Article number: 116, pp. 1 - 5 [articolo]Open Access
R. Liguori;M. P. Giannoccaro;A. Arnoldi;A. Citterio;C. Tonon;R. Lodi;N. Bresolin;M. T. Bassi, Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations., «JOURNAL OF NEUROLOGY», 2014, 261, pp. 1789 - 1793 [articolo]
E. Boschetti; R. D’Alessandro; F. Bianco; V. Carelli; G. Cenacchi; A.D. Pinna; M. Del Gaudio; R. Rinaldi; V. Stanghellini; C. Tonon; R. Lodi; L. Pironi; K. Rhoden; V. Tugnoli; C. Casali; R. De Giorgio, Liver tissue: a proof-of-concept study for OLT in MNGIE patients, «EUROPEAN JOURNAL OF HISTOCHEMISTRY», 2014, 58, pp. 8 - 8 [abstract]
