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Results: 1-6 |
Results: 6

Authors: Monti, L Salerno, T Lucidi, V Fariello, G Orazi, C Manfredi, R Bella, S Castro, M
Citation: L. Monti et al., Pancreatic cystosis in cystic fibrosis: case report, ABDOM IMAG, 26(6), 2001, pp. 648-650

Authors: Di Capua, M Lispi, ML Giannotti, A Longo, D Fariello, G
Citation: M. Di Capua et al., Neurofibromatosis type 1 presenting with hand dystonia, J CHILD NEU, 16(8), 2001, pp. 606-608

Authors: Giacco, G Cannata, V Furetta, C Santopietro, F Fariello, G
Citation: G. Giacco et al., On the use of pediatric phantoms in the dose evaluation during computed tomography (CT) thorax examinations, MED PHYS, 28(2), 2001, pp. 199-204

Authors: Salvi, S Santorelli, FM Bertini, E Boldrini, R Meli, C Donati, A Burlina, AB Rizzo, C Di Capua, M Fariello, G Dionisi-Vici, C
Citation: S. Salvi et al., Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome, NEUROLOGY, 57(5), 2001, pp. 911-914

Authors: Francalanci, P Eymard-Pierre, E Dionisi-Vici, C Boldrini, R Piemonte, F Virgili, R Fariello, G Bosman, C Santorelli, FM Boespflug-Tanguy, O Bertini, E
Citation: P. Francalanci et al., Fatal infantile leukodystrophy - A severe variant of CACH/VWM syndrome, allelic to chromosome 3q27, NEUROLOGY, 57(2), 2001, pp. 265-270

Authors: Bertini, E des Portes, V Zanni, G Santorelli, F Dionisi-Vici, C Vicari, S Fariello, G Chelly, J
Citation: E. Bertini et al., X-linked congenital ataxia: A clinical and genetic study, AM J MED G, 92(1), 2000, pp. 53-56
Risultati: 1-6 |