CAMA, ARMANDO

CAMA, ARMANDO  

100009 - Dipartimento di Neuroscienze, Riabilitazione, Oftamologia, Genetica e Scienze Materno-Infantili  

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A 3-year-old boy with drug-resistant complex partial seizures 1-gen-2012 Striano, Pasquale; Consales, A; Severino, M; Prato, G; Occella, C; Rossi, A; Cama, A; Nozza, P; Baglietto, MARIA GIUSEPPINA
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 1-gen-2019 Salpietro, V; Dixon, Cl; Guo, H; Bello, Od; Vandrovcova, J; Efthymiou, S; Maroofian, R; Heimer, G; Burglen, L; Valence, S; Torti, E; Hacke, M; Rankin, J; Tariq, H; Colin, E; Procaccio, V; Striano, P; Mankad, K; Lieb, A; Chen, S; Pisani, L; Bettencourt, C; Männikkö, R; Manole, A; Brusco, A; Grosso, E; Ferrero, Gb; Armstrong-Moron, J; Gueden, S; Bar-Yosef, O; Tzadok, M; Monaghan, Kg; Santiago-Sim, T; Person, Re; Cho, Mt; Willaert, R; Yoo, Y; Chae, Jh; Quan, Y; Wu, H; Wang, T; Bernier, Ra; Xia, K; Blesson, A; Jain, M; Motazacker, Mm; Jaeger, B; Schneider, Al; Boysen, K; Muir, Am; Myers, Ct; Gavrilova, Rh; Gunderson, L; Schultz-Rogers, L; Klee, Ew; Dyment, D; Osmond, M; Parellada, M; Llorente, C; Gonzalez-Peñas, J; Carracedo, A; Van Haeringen, A; Ruivenkamp, C; Nava, C; Heron, D; Nardello, R; Iacomino, M; Minetti, C; Skabar, A; Fabretto, A; SYNAPS Study, Group; Raspall-Chaure, M; Chez, M; Tsai, A; Fassi, E; Shinawi, M; Constantino, Jn; De Zorzi, R; Fortuna, S; Kok, F; Keren, B; Bonneau, D; Choi, M; Benzeev, B; Zara, F; Mefford, Hc; Scheffer, Ie; Clayton-Smith, J; Macaya, A; Rothman, Je; Eichler, Ee; Kullmann, Dm; Houlden, H; Hanna, Mg; Bugiardini, E; Hostettler, I; O'Callaghan, B; Khan, A; Cortese, A; O'Connor, E; Yau, Wy; Bourinaris, T; Kaiyrzhanov, R; Chelban, V; Madej, M; Diana, Mc; Vari, Ms; Pedemonte, M; Bruno, C; Balagura, G; Scala, M; Fiorillo, C; Nobili, L; Malintan, Nt; Zanetti, Mn; Krishnakumar, Ss; Lignani, G; Jepson, Jec; Broda, P; Baldassari, S; Rossi, P; Fruscione, F; Madia, F; Traverso, M; De-Marco, P; Pérez-Dueñas, B; Munell, F; Kriouile, Y; El-Khorassani, M; Karashova, B; Avdjieva, D; Kathom, H; Tincheva, R; Van-Maldergem, L; Nachbauer, W; Boesch, S; Gagliano, A; Amadori, E; Goraya, Js; Sultan, T; Kirmani, S; Ibrahim, S; Jan, F; Mine, J; Banu, S; Veggiotti, P; Zuccotti, Gv; Ferrari, Md; Van Den Maagdenberg, Amj; Verrotti, A; Marseglia, Gl; Savasta, S; Soler, Ma; Scuderi, C; Borgione, E; Chimenz, R; Gitto, E; Dipasquale, V; Sallemi, A; Fusco, M; Cuppari, C; Cutrupi, Mc; Ruggieri, M; Cama, A; Capra, V; Mencacci, Ne; Boles, R; Gupta, N; Kabra, M; Papacostas, S; Zamba-Papanicolaou, E; Dardiotis, E; Maqbool, S; Rana, N; Atawneh, O; Lim, Sy; Shaikh, F; Koutsis, G; Breza, M; Coviello, Da; Dauvilliers, Ya; Alkhawaja, I; Alkhawaja, M; Al-Mutairi, F; Stojkovic, T; Ferrucci, V; Zollo, M; Alkuraya, Fs; Kinali, M; Sherifa, H; Benrhouma, H; Turki, Iby; Tazir, M; Obeid, M; Bakhtadze, S; Saadi, Nw; Zaki, Ms; Triki, Cc; Benfenati, F; Gustincich, S; Kara, M; Belcastro, V; Specchio, N; Capovilla, G; Karimiani, Eg; Salih, Am; Okubadejo, Nu; Ojo, Oo; Oshinaike, Oo; Oguntunde, O; Wahab, K; Bello, Ah; Abubakar, S; Obiabo, Y; Nwazor, E; Ekenze, O; Williams, U; Iyagba, A; Taiwo, L; Komolafe, M; Senkevich, K; Shashkin, C; Zharkynbekova, N; Koneyev, K; Manizha, G; Isrofilov, M; Guliyeva, U; Salayev, K; Khachatryan, S; Rossi, S; Silvestri, G; Haridy, N; Ramenghi, La; Xiromerisiou, G; David, E; Aguennouz, M; Fidani, L; Spanaki, C; Tucci, A.
Analysis of NADP+-dependent isocitrate dehydrogenase-1/2 gene mutations in pediatric brain tumors: Report of a secondary anaplastic astrocytoma carrying the IDH1 mutation 1-gen-2012 Mascelli, S.; Raso, A.; Biassoni, R.; Severino, M.; Sak, K.; Joost, K.; Milanaccio, C.; Barra, S.; Grillo-Ruggieri, F.; Vanni, I.; Consales, A.; Cama, A.; Capra, V.; Nozza, P.; Garre, M. L.
Brain damage as detected by cDNA-microarray in the spinal fluid of patients with aicardi-goutières syndrome 1-gen-2008 Izzotti, A.; Fazzi, E.; Orcesi, S.; Cartiglia, C.; Longobardi, M.; Capra, V.; Lebon, P.; Cama, A.; Pulliero, A.; La Piana, R.; Lanzi, G.
Brain damage as detected by cDNA-microarray in the spinal fluid of patients with Aicardi-Goutieres syndrome 1-gen-2008 Izzotti, Alberto; Fazzi, E.; Orcesi, S.; Cartiglia, Cristina; Longobardi, Mariagrazia; Capra, V.; Lebon, P.; Cama, A.; Pulliero, Alessandra; LA PIANA, R.; Lanzi, G.
Burr Holes Revascularization in Three Pediatric Cases of Moyamoya Syndrome: Easy Choice or Insidious Trap? Case Series and Review 1-gen-2018 Pacetti, Mattia; Tortora, Domenico; Fiaschi, Pietro; Consales, Alessandro; Piatelli, Gianluca; Ravegnani, Marcello; Cama, Armando; Pavanello, Marco
Chiari malformation type I: what information from the genetics? 1-gen-2019 Capra, V.; Iacomino, M.; Accogli, A.; Pavanello, M.; Zara, F.; Cama, A.; De Marco, P.
Consensus statement from the international consensus meeting on post-traumatic cranioplasty 1-gen-2021 Iaccarino, C.; Kolias, A.; Adelson, P. D.; Rubiano, A. M.; Viaroli, E.; Buki, A.; Cinalli, G.; Fountas, K.; Khan, T.; Signoretti, S.; Waran, V.; Adeleye, A. O.; Amorim, R.; Bertuccio, A.; Cama, A.; Chesnut, R. M.; De Bonis, P.; Estraneo, A.; Figaji, A.; Florian, S. I.; Formisano, R.; Frassanito, P.; Gatos, C.; Germano, A.; Giussani, C.; Hossain, I.; Kasprzak, P.; La Porta, F.; Lindner, D.; Maas, A. I. R.; Paiva, W.; Palma, P.; Park, K. B.; Peretta, P.; Pompucci, A.; Posti, J.; Sengupta, S. K.; Sinha, A.; Sinha, V.; Stefini, R.; Talamonti, G.; Tasiou, A.; Zona, G.; Zucchelli, M.; Hutchinson, P. J.; Servadei, F.
Craniosinostosi 1-gen-1996 Bonioli, Eugenio; Cama, A.; Bellini, C.
Currarino syndrome: Proposal of a diagnostic and therapeutic protocol 1-gen-2004 Martucciello, Giuseppe; Torre, M.; Belloni, E.; Lerone, M.; PINI PRATO, A.; Cama, A.; Jasonni, Vincenzo
Dermoid and Epidermoid Cysts of Scalp: Case Series of 234 Consecutive Patients 1-gen-2018 Prior, A.; Anania, P.; Pacetti, M.; Secci, F.; Ravegnani, M.; Pavanello, M.; Piatelli, G.; Cama, A.; Consales, A.
A Distinct Gene-Expression Profile in Pediatric Ganglioglioma 1-gen-2012 Samantha, Mascelli; Alessandro, Raso; Barla, Annalisa; Paolo, Nozza; Roberto, Biassoni; Sara, Pignatelli; Cama, Armando; Verri, Alessandro; Valeria, Capra; Marialuisa, Garrè
Distinctive Genetic Profile With IDH1, TP53, and MLH1 Mutations in a Radiation-Induced Anaplastic Astrocytoma 1-gen-2016 Mascelli, S.; Nozza, P.; Sak, K.; Joost, K.; Cama, A.; Capra, V.; Garre, M. L.; Raso, A.
Endocrine and growth features in childhood craniopharyngioma: a mono-institutional study. 1-gen-2006 DI BATTISTA, ELIANA MARIA; Naselli, Arturo; Queirolo, S; Gallarotti, F; Garre', Ml; Milanaccio, C; Cama, A.
Epilepsy associated with supratentorial brain tumors under 3 years of life. 1-gen-2009 Gaggero, R; Consales, A; Fazzini, F; Mancardi, Mm; Baglietto, MARIA GIUSEPPINA; Nozza, P; Rossi, A; Pistorio, A; Tumolo, M; Cama, A; Garrè, Ml; Striano, Pasquale
Erratum to: Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 1-gen-2009 Consales, A.; Piatelli, G.; Ravegnani, M.; Pavanello, M.; Striano, Pasquale; Zoli, M. L.; Capra, V.; Rossi, A.; Garrè, M. L.; Calevo, M. G.; Cama, A.
Exclusion of the Sonic Hedgeog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopment 1-gen-1999 Seri, M.; Martucciello, Giuseppe; Paleari, L.; Bolino, A.; Priolo, M.; Salemi, G.; Forabosco, P.; Caroli, F.; Cusano, R.; Tocco, T.; Lerone, M.; Cama, A.; Torre, M.; Guys, Jm; Romeo, G.; Jasonni, Vincenzo
Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type i reveals candidate genes for cranio-facial development 1-gen-2017 Merello, E; Tattini, L; Magi, A; Accogli, 1; Piatelli, G; Pavanello, M; Tortora, Domenico; Cama, Armando; Kibar, Z; Capra, V; DE MARCO, Patrizia
Final results of the second prospective AIEOP protocol for pediatric intracranial ependymoma 1-gen-2016 Massimino, M.; Miceli, R.; Giangaspero, F.; Boschetti, L.; Modena, P.; Antonelli, M.; Ferroli, P.; Bertin, D.; Pecori, E.; Valentini, L.; Biassoni, V.; Garre, M. L.; Schiavello, E.; Sardi, I.; Cama, A.; Viscardi, E.; Scarzello, G.; Scoccianti, S.; Mascarin, M.; Quaglietta, L.; Cinalli, G.; Diletto, B.; Genitori, L.; Peretta, P.; Mussano, A.; Buccoliero, A.; Calareso, G.; Barra, S.; Mastronuzzi, A.; Giussani, C.; Marras, C. E.; Balter, R.; Bertolini, P.; Giombelli, E.; La Spina, M.; Buttarelli, F. R.; Pollo, B.; Gandola, L.
FOCAL PHARMACORESISTANT EPILEPSY IN A CHILD WITH NEUROCUTANEOUS MELANOSIS 1-gen-2011 Pezzella, M; Prato, G; Giudizioso, G; Consales, A; Cama, A; Severino, M; Striano, Pasquale; Baglietto, MARIA GIUSEPPINA