| Spinal dysraphism: a review of neuroradiological features with embryological correlations and proposal for a new classification P Tortori-Donati, A Rossi, A Cama Neuroradiology 42, 471-491, 2000 | 443 | 2000 |
| Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly S Brunelli, A Faiella, V Capra, V Nigro, A Simeone, A Cama, E Boncinelli Nature genetics 12 (1), 94-96, 1996 | 354 | 1996 |
| Germline mutations of the APC gene in patients with familial adenomatous polyposis-associated thyroid carcinoma: results from a European cooperative study F Cetta, G Montalto, M Gori, MC Curia, A Cama, S Olschwang The Journal of Clinical Endocrinology & Metabolism 85 (1), 286-292, 2000 | 300 | 2000 |
| Tyr612 and Tyr632 in Human Insulin Receptor Substrate-1 Are Important for Full Activation of Insulin-Stimulated Phosphatidylinositol 3-Kinase Activity and … DL Esposito, Y Li, A Cama, MJ Quon Endocrinology 142 (7), 2833-2840, 2001 | 203 | 2001 |
| BRCA1 and BRCA2 mutation status and tumor characteristics in male breast cancer: a population-based study in Italy L Ottini, G Masala, C D’Amico, B Mancini, C Saieva, G Aceto, D Gestri, ... Cancer Research 63 (2), 342-347, 2003 | 197 | 2003 |
| Craniopharyngioma: modern concepts in pathogenesis and treatment ML Garrè, A Cama Current opinion in pediatrics 19 (4), 471-479, 2007 | 191 | 2007 |
| AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders V Salpietro, CL Dixon, H Guo, OD Bello, J Vandrovcova, S Efthymiou, ... Nature communications 10 (1), 3094, 2019 | 184 | 2019 |
| Imaging in spine and spinal cord malformations A Rossi, R Biancheri, A Cama, G Piatelli, M Ravegnani, P Tortori-Donati European journal of radiology 50 (2), 177-200, 2004 | 180 | 2004 |
| Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population P De Marco, MG Calevo, A Moroni, L Arata, E Merello, RH Finnell, H Zhu, ... Journal of human genetics 47 (6), 319-324, 2002 | 179 | 2002 |
| VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5 D Szumska, G Pieles, R Essalmani, M Bilski, D Mesnard, K Kaur, ... Genes & development 22 (11), 1465-1477, 2008 | 158 | 2008 |
| Currarino syndrome: proposal of a diagnostic and therapeutic protocol G Martucciello, M Torre, E Belloni, M Lerone, AP Prato, A Cama, ... Journal of pediatric surgery 39 (9), 1305-1311, 2004 | 144 | 2004 |
| Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome—a new clinical perspective ML Garre, A Cama, F Bagnasco, G Morana, F Giangaspero, M Brisigotti, ... Clinical Cancer Research 15 (7), 2463-2471, 2009 | 133 | 2009 |
| Segmental spinal dysgenesis: neuroradiologic findings with clinical and embryologic correlation P Tortori-Donati, MP Fondelli, A Rossi, CA Raybaud, A Cama, V Capra American journal of neuroradiology 20 (3), 445-456, 1999 | 133 | 1999 |
| Final results of the second prospective AIEOP protocol for pediatric intracranial ependymoma M Massimino, R Miceli, F Giangaspero, L Boschetti, P Modena, ... Neuro-oncology 18 (10), 1451-1460, 2016 | 123 | 2016 |
| Magnetic resonance imaging of spinal dysraphism P Tortori-Donati, A Rossi, R Biancheri, A Cama Topics in Magnetic Resonance Imaging 12 (6), 375-409, 2001 | 123 | 2001 |
| Reduced folate carrier polymorphism (80A→ G) and neural tube defects P De Marco, MG Calevo, A Moroni, E Merello, A Raso, RH Finnell, H Zhu, ... European journal of human genetics 11 (3), 245-252, 2003 | 120 | 2003 |
| Spinal dysraphism: MR imaging rationale A Rossi, A Cama, G Piatelli, M Ravegnani, R Biancheri, P Tortori-Donati Journal of neuroradiology 31 (1), 3-24, 2004 | 110 | 2004 |
| Hyperfractionated radiotherapy and chemotherapy for childhood ependymoma: final results of the first prospective AIEOP (Associazione Italiana di Ematologia-Oncologia Pediatrica … M Massimino, L Gandola, F Giangaspero, A Sandri, P Valagussa, ... International Journal of Radiation Oncology* Biology* Physics 58 (5), 1336-1345, 2004 | 109 | 2004 |
| Magnetic resonance imaging spectrum of medulloblastoma J Fruehwald-Pallamar, SB Puchner, A Rossi, ML Garre, A Cama, ... Neuroradiology 53, 387-396, 2011 | 108 | 2011 |
| FZD6 is a novel gene for human neural tube defects P De Marco, E Merello, A Rossi, G Piatelli, A Cama, Z Kibar, V Capra Human mutation 33 (2), 384-390, 2012 | 106 | 2012 |
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