Armando Cama
Armando Cama
Istituto Giannina Gaslini, Genoa (Italy)
Verified email at gaslini.org
TitleCited byYear
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, 1996
3131996
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 (7), 471-491, 2000
2812000
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
2412000
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
1572001
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, 2002
1482002
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
1422003
Craniopharyngioma: modern concepts in pathogenesis and treatment
ML Garrč, A Cama
Current opinion in pediatrics 19 (4), 471-479, 2007
1222007
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
1122008
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
1072004
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
1062004
Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome—a new clinical perspective
ML Garrč, A Cama, F Bagnasco, G Morana, F Giangaspero, M Brisigotti, ...
Clinical Cancer Research 15 (7), 2463-2471, 2009
1052009
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
1011999
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, 2003
992003
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
942001
Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G> A polymorphism for neural tube defect risk
P De Marco, E Merello, MG Calevo, S Mascelli, A Raso, A Cama, V Capra
Journal of human genetics 51 (2), 98-103, 2006
882006
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
852004
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
792004
Chiari complex in children-neuroradiological diagnosis, neurosurgical treatment and proposal of a new classification (312 cases)
A Cama, P Tortori-Donati, GL Piatelli, MP Fondelli, L Andreussi
European Journal of Pediatric Surgery 5 (S 1), 35-38, 1995
781995
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
692012
Polymorphisms in genes involved in folate metabolism as risk factors for NTDs
P De Marco, MG Calevo, A Moroni, L Arata, E Merello, A Cama, ...
European Journal of Pediatric Surgery 11 (S1), S14-S17, 2001
692001
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