Carrozzo, Rosalba; Verrigni, Daniela; Rasmussen, Magnhild; de Coo, Rene; Amartino, Hernan; Bianchi, Marzia; Buhas, Daniela; Mesli, Samir; Naess, Karin; Born, Alfred Peter; Woldseth, Berit; Prontera, Paolo; Batbayli, Mustafa; Ravn, Kirstine; Joensen, Fróði; Cordelli, Duccio M.; Santorelli, Filippo Maria; Tulinius, Mar; Darin, Niklas; Duno, Morten; Jouvencel, Philippe; Burlina, Alberto; Stangoni, Gabriela; Bertini, Enrico; Redonnet-Vernhet, Isabelle; Wibrand, Flemming; Dionisi-Vici, Carlo; Uusimaa, Johanna; Vieira, Paivi; Osorio, Andrés Nascimento; McFarland, Robert; Taylor, Robert W.; Holme, Elisabeth; Ostergaard, Elsebet*, Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients, «JOURNAL OF INHERITED METABOLIC DISEASE», 2016, 39, pp. 243 - 252 [Scientific article]
Magini, Pamela; Poscente, Monica; Ferrari, Simona; Vargiolu, Manuela; Bacchelli, Elena; Graziano, Claudio; Wischmeijer, Anita; Turchetti, Daniela; Malaspina, Elisabetta; Marchiani, Valentina; Cordelli, Duccio Maria; Franzoni, Emilio; Romeo, Giovanni; Seri, Marco, Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration, «MOLECULAR CYTOGENETICS», 2015, 8, Article number: 58 , pp. 1 - 7 [Scientific article]Open Access
Masetti, Riccardo; Cordelli, Duccio Maria; Zama, Daniele; Vendemini, Francesca; Biagi, Carlotta; Franzoni, Emilio; Pession, Andrea, PRES in children undergoing hematopoietic stem cell or solid organ transplantation, «PEDIATRICS», 2015, 135, pp. 890 - 901 [Scientific article]
Magini P;Pippucci T;Tsai IC;Coppola S;Stellacci E;Bartoletti-Stella A;Turchetti D;Graziano C;Cenacchi G;Neri I;Cordelli DM;Marchiani V;Bergamaschi R;Gasparre G;Neri G;Mazzanti L;Patrizi A;Franzoni E;Romeo G;Bordo D;Tartaglia M;Katsanis N;Seri M, A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype., «HUMAN MOLECULAR GENETICS», 2014, 23, pp. 3607 - 3617 [Scientific article]
Raffaella Vergaro;Duccio Maria Cordelli;Angela Miniaci;Davide Tassinari;Luca Spinardi;Andrea Pession;Emilio Franzoni, Cerebral Ischemic Involvement in Vogt-Koyanagi-Harada Disease, «PEDIATRIC NEUROLOGY», 2014, 51, pp. 119 - 122 [Scientific article]
Duccio Maria Cordelli;Riccardo Masetti;Daniele Zama;Daniela Gueraldi;Roberto Rondelli;Carlo Cottone;Arcangelo Prete;Andrea Pession;Emilio Franzoni, Etiology, characteristics and outcome of seizures after pediatric hematopoietic stem cell transplantation, «SEIZURE», 2014, 23, pp. 140 - 145 [Scientific article]
Zama D;Morello W;Masetti R;Cordelli DM;Massaccesi E;Prete A;Pession A, Inflammatory disease of the central nervous system induced by anti-GD2 monoclonal antibody in a patient with high risk neuroblastoma., «PEDIATRIC BLOOD & CANCER», 2014, 61, pp. 1521 - 1522 [Scientific article]
Livingston, John H.*; Mayer, Josephine; Jenkinson, Emma; Kasher, Paul; Stivaros, Stavros; Berger, Andrea; Cordelli, Duccio M.; Ferreira, Patrick; Jefferson, Rosalind; Kutschke, Georg; Lundberg, Staffan; Ounap, Katrin; Prabhakar, Prab; Soh, Calvin; Stewart, Helen; Stone, Jon; Van Der Knaap, Marjo S.; Van Esch, Hilda; Van Mol, Christine; Wakeling, Emma; Whitney, Andrea; Rice, Gillian I.; Crow, Yanick J., Leukoencephalopathy with calcifications and cysts: A purely neurological disorder distinct from coats plus, «NEUROPEDIATRICS», 2014, 45, pp. 175 - 182 [Scientific article]
Duccio M. Cordelli; Riccardo Masetti; Emilia Ricci; Francesco Toni; Daniele Zama; Monica Maffei; Andrea Gentili; Antonia Parmeggiani; Andrea Pession; Emilio Franzoni, Life-threatening complications of posterior
reversible encephalopathy syndrome in children, «EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY», 2014, 18, pp. 632 - 640 [Scientific article]
Zama, D; Masetti, R; Cordelli, Dm; Vendemini, F; Giordano, L; Milito, G; Franzoni, E; Porta, F; Prete, A; Rondelli, R; Pession A., Risk factor analysis of posterior reversible encephalopathy syndrome after allogeneic hematopoietic SCT in children, «BONE MARROW TRANSPLANTATION», 2014, 49, pp. 1538 - 1540 [Scientific article]
Quattrocchi, Carlo C.; Zanni, Ginevra; Napolitano, Antonio; Longo, Daniela; Cordelli, Duccio Maria; Barresi, Sabina; Randisi, Francesco; Valente, Enza Maria; Verdolotti, Tommaso; Genovese, Elisabetta; Specchio, Nicola; Vitiello, Giuseppina; Spiegel, Ronen; Bertini, Enrico; Bernardi, Bruno*, Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: Further delineation of a cobblestone-like phenotype, «NEUROGENETICS», 2013, 14, pp. 77 - 83 [Scientific article]
Giordano, Lucio*; Vignoli, Aglaia; Cusmai, Raffaella; Parisi, Pasquale; Mastrangelo, Massimo; Coppola, Giangennaro; Cordelli, Duccio Maria; Accorsi, Patrizia; Milito, Giuseppe; Darra, Francesca; Pruna, Dario; Belcastro, Vincenzo; Verrotti, Alberto; Striano, Pasquale, Early onset absence epilepsy with onset in the first year of life: A multicenter cohort study, «EPILEPSIA», 2013, 54, pp. 66 - 69 [Scientific article]
Cordelli DM; Garavelli L; Savasta S; Guerra A; Pellicciari A; Giordano L; Bonetti S; Cecconi I; Wischmeijer A; Seri M; Rosato S; Gelmini C; Della Giustina E; Ferrari AR; Zanotta N; Epifanio R; Grioni D; Malbora B; Mammi I; Mari F; Buoni S; Mostardini R; Grosso S; Pantaleoni C; Doz M; Poch-Olivé ML; Rivieri F; Sorge G; Simonte G; Licata F; Tarani L; Terazzi E; Mazzanti L; Cerruti Mainardi P; Boni A; Faravelli F; Grasso M; Bianchi P; Zollino M; Franzoni E., Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype., «AMERICAN JOURNAL OF MEDICAL GENETICS. PART A», 2013, 161A, pp. 273 - 284 [Scientific article]
Cordelli DM; Pellicciari A; Kiriazopulos D; Franzoni E; Garavelli L., Epilepsy
in Mowat-Wilson syndrome: is it a matter of GABA?, «EPILEPSIA», 2013, 54(7), pp. 1331 - 1332 [Scientific article]
Cordelli DM; Aldrovandi A; Gentile V; Garone C; Conti S; Aceti A; Gennaro E;
Zara F; Franzoni E, Fever as a seizure precipitant factor in Panayiotopoulos
syndrome: A clinical and genetic study, «SEIZURE», 2012, 21(2), pp. 141 - 143 [Scientific article]
