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Dott. Fabiano Carmelo - Azienda Ospedaliera Ospedali Riuniti Villa ...

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Pubblicazioni scientifiche 19. Long-Term Efficacy of α-Interferon in β-Thalassemics With Chornic Hepatitis CV Di Marco, O Lo Iacono, P Almasio, C Ciaccio, M Capra, M Rizzo, R Malizia, A Maggio,C <strong>Fabiano</strong>, F Barbaria, A Craxi’. Blood, vol 90, n 6, pag 2207-2212, september 15,1997.20. Long-term course of interferon-treated chronic hepatitis CC Camma’, V Di Marco, O Lo Iacono, P Almasio, M Giunta, P Fuschi, A Vaccaro, C <strong>Fabiano</strong>,S Magrin, R Di Stefano, C Bonura, L Pagliaro, A Craxi’. J of Hepatology 28, pag 531-537,1998.21. Rapid molecular diagnosis of G6PD variants using multiplex PCR and Reverse DotBlot analysis.P Sammarco, C <strong>Fabiano</strong>, F Giardina, G Corsello. Ital J Pediatr 2002, 28: 396-40022. Identification of a New Nonsense Mutation (Tyr129Stop) of the SRY Gene in aNewborn Infant With XY Sex-ReversalM Giuffrè, P Sammarco, C <strong>Fabiano</strong>, F Giardina, F Lunetta, G Corsello Am J Medical Genetics128A: 46-47 200423. Rapid molecular diagnosis of Gilbert’s SyndromeP Sammarco, C <strong>Fabiano</strong>, F Giardina, M Giuffrè, M Piccione, G Corsello. Italian GiournalPediatric 2004; 30 245-247.24. Epidemiological Study of Nonsyndromic Hearing Loss in Sicilian NewbornsM Niceta, C <strong>Fabiano</strong>, P Sammarco, M Piccione, V Antona, M Giuffrè and G Corsello.Am J Medical Genetics vol 143A, n°14, July 15, 2007, p1666-1670.25.Familial Mediterranean fever gene (MEVF) mutations in Chron’s disease in aMediterranean area.Renda MC, Civitavecchia G, <strong>Fabiano</strong> C, Sammarco P, Cottone M. Inflamm Bowel Dis.2008sept;14(9):1313.26.An uncommon case of a female carrier of two distinct X-linked disorders<strong>Fabiano</strong> C, Acquila M, Bicocchi MP, Sammarco P. Haemophilia.2008 May;14(3):665-6.27.Acalculous cholecystitis during the course of acute Epstein-Barr virus infection andGilbert’s syndrome.Iaria C, Leonardi MS, <strong>Fabiano</strong> C, Cascio A.Int J Infect Dis, 2009 Nov;13(6):e519-20.28.Q289P mutation in the FGFR2 gene:first report in a patient with type 1 Pfeiffersyndrome.Piccione M, Antona V, Niceta M, <strong>Fabiano</strong> C, Martines M, Bianchi A, Corsello G. Eur J Pediatr.2009 Sep;168(9):1135-9.29.Trombofilia ereditaria e complicanze gravidiche nella popolazione siciliana.W.O Bertolino, F. Labate, E.C. Bertolino, M.Rannazzisi, G. Assadi, P. Sammarco, M. Niceta,C.<strong>Fabiano</strong>. Italian Journal Gynaecol Obstetr 21:N3:129-136,200930.Persistent jaundice in an infant with homozygous beta-thalassemia due toc o-inheritedCrigler-Najjar syndrome.Aggarwal V, Seth A, Sherma S, Aneja S, Sammarco P, <strong>Fabiano</strong> C. Pediatr Blood Cancer, 2009Dec1 2010;54:627-62831.Glucose 6-phosphate dehydrogenase Palermo R257M; a novel variant associated withchronic non-spherocytic haemolytic anaemia.P Rigano, C <strong>Fabiano</strong>, F Pojero, M Niceta, A Pecoraro, A Maggio, P Sammarco.British Journal of Haematology, Vol.149:2, 2010 Apr 2.32.Cardiopatie congenite e mutazioni genetiche nella popolazione siciliana: casi clinici.EC Bertolino, G Murana, V Billone, V Cigna, M Rannazzisi, OW Bertolino, F.Enia, C <strong>Fabiano</strong>, MNiceta, P Sammarco. Giornale Italiano di Cardiologia Pratica, Anno 9 numero 3-4, Lug-Dic2010.FirmaIl sottoscritto è consapevole delle sanzioni in caso di dichiarazione mendace (ai sensidell’art.76 del DPR 28 dicembre 2000 n.445). Inoltre, il sottoscritto autorizza al trattamentodei dati personali, secondo quanto previsto dal Decreto Legislativo n° 196 del 30 giugno2003 e successive modifiche.<strong>Carmelo</strong> <strong>Fabiano</strong>Pagina 4/4 - Curriculum vitae di<strong>Carmelo</strong> dott <strong>Fabiano</strong>

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