CAMA, ARMANDO
CAMA, ARMANDO
100009 - Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno-Infantili
A 3-year-old boy with drug-resistant complex partial seizures
2012-01-01 Striano, Pasquale; Consales, A; Severino, M; Prato, G; Occella, C; Rossi, A; Cama, A; Nozza, P; Baglietto, MARIA GIUSEPPINA
A Novel Skin and Fascia Opening for Subfascial Inserting of Intrathecal Baclofen Pump
2018-01-01 Fiaschi, P.; Cama, A.; Piatelli, G.; Moretti, P.; Pavanello, M.
A rare case of osteoblastoma associated to aneurysmal bone cyst of the spine. Case report
2016-01-01 Pavanello, Marco; Melloni, Ilaria; Fiaschi, Pietro; Consales, Alessandro; Piatelli, Gianluca; Ravegnani, Marcello; Nozza, Paolo; Gandolfo, Carlo; Cama, Armando
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
2019-01-01 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
2012-01-01 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-Goutieres syndrome
2008-01-01 Izzotti, Alberto; Fazzi, E.; Orcesi, S.; Cartiglia, Cristina; Longobardi, Mariagrazia; Capra, V.; Lebon, P.; Cama, A.; Pulliero, Alessandra; LA PIANA, R.; Lanzi, G.
Brain damage as detected by cDNA-microarray in the spinal fluid of patients with aicardi-goutières syndrome
2008-01-01 Izzotti, A.; Fazzi, E.; Orcesi, S.; Cartiglia, C.; Longobardi, M.; Capra, V.; Lebon, P.; Cama, A.; Pulliero, A.; La Piana, R.; Lanzi, G.
Burr Holes Revascularization in Three Pediatric Cases of Moyamoya Syndrome: Easy Choice or Insidious Trap? Case Series and Review
2018-01-01 Pacetti, Mattia; Tortora, Domenico; Fiaschi, Pietro; Consales, Alessandro; Piatelli, Gianluca; Ravegnani, Marcello; Cama, Armando; Pavanello, Marco
Caudal regression syndrome: An online multicentre survey. Urological long-term results
2002-01-01 Buffa, P.; Torre, M.; Scarsi, P. L.; De Gennaro, M.; Battaglino, F.; Beseghi, U.; Di Lorenzo, F.; Cama, A.
Chiari malformation type I: what information from the genetics?
2019-01-01 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
2021-01-01 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.
Currarino syndrome: Proposal of a diagnostic and therapeutic protocol
2004-01-01 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
2018-01-01 Prior, A.; Anania, P.; Pacetti, M.; Secci, F.; Ravegnani, M.; Pavanello, M.; Piatelli, G.; Cama, A.; Consales, A.
Distinctive Genetic Profile With IDH1, TP53, and MLH1 Mutations in a Radiation-Induced Anaplastic Astrocytoma
2016-01-01 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.
2006-01-01 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.
2009-01-01 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.
2009-01-01 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 Hedgehog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopment
1999-01-01 Seri, M.; Martucciello, G.; Paleari, L.; Bolino, A.; Priolo, M.; Salemi, G.; Forabosco, P.; Caroli, F.; Cusano, R.; Tocco, T.; Lerone, M.; Cama, A.; Torre, M.; Guys, J. M.; Romeo, G.; Jasonni, V.
Exclusion of the Sonic Hedgeog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopment
1999-01-01 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
2017-01-01 Merello, E; Tattini, L; Magi, A; Accogli, 1; Piatelli, G; Pavanello, M; Tortora, Domenico; Cama, Armando; Kibar, Z; Capra, V; DE MARCO, Patrizia
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| A Novel Skin and Fascia Opening for Subfascial Inserting of Intrathecal Baclofen Pump | 1-gen-2018 | Fiaschi, P.; Cama, A.; Piatelli, G.; Moretti, P.; Pavanello, M. | |
| A rare case of osteoblastoma associated to aneurysmal bone cyst of the spine. Case report | 1-gen-2016 | Pavanello, Marco; Melloni, Ilaria; Fiaschi, Pietro; Consales, Alessandro; Piatelli, Gianluca; Ravegnani, Marcello; Nozza, Paolo; Gandolfo, Carlo; Cama, Armando | |
| 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-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. | |
| 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. | |
| 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 | |
| Caudal regression syndrome: An online multicentre survey. Urological long-term results | 1-gen-2002 | Buffa, P.; Torre, M.; Scarsi, P. L.; De Gennaro, M.; Battaglino, F.; Beseghi, U.; Di Lorenzo, F.; Cama, A. | |
| 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. | |
| 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. | |
| 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 Hedgehog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopment | 1-gen-1999 | Seri, M.; Martucciello, G.; Paleari, L.; Bolino, A.; Priolo, M.; Salemi, G.; Forabosco, P.; Caroli, F.; Cusano, R.; Tocco, T.; Lerone, M.; Cama, A.; Torre, M.; Guys, J. M.; Romeo, G.; Jasonni, V. | |
| 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 |