Authors: De Gobbi, M Barilaro, MR Garozzo, G Sbaiz, L Alberti, F Camaschella, C

Citation: M. De Gobbi et al., TFR2 Y250X mutation in Italy, BR J HAEM, 114(1), 2001, pp. 243-244

Authors: Roetto, A Totaro, A Piperno, A Piga, A Longo, F Garozzo, G Cali, A De Gobbi, M Gasparini, P Camaschella, C

Citation: A. Roetto et al., New mutations inactivating transferrin receptor 2 in hemochromatosis type 3, BLOOD, 97(9), 2001, pp. 2555-2560

Authors: Restagno, G Gomez, AM Sbaiz, L De Gobbi, M Roetto, A Bertino, E Fabris, C Fiorucci, GC Fortina, P Camaschella, C

Citation: G. Restagno et al., A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan (TM)technology, GENET TEST, 4(2), 2000, pp. 177-181

Authors: Camaschella, C Roetto, A Cali, A De Gobbi, M Garozzo, G Carella, M Majorano, N Totaro, A Gasparini, P

Citation: C. Camaschella et al., The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22, NAT GENET, 25(1), 2000, pp. 14-15

Authors: De Gobbi, M Pasquero, P Brunello, F Paccotti, P Mazza, U Camaschella, C

Citation: M. De Gobbi et al., Juvenile hemochromatosis associated with beta-thalassemia treated by phlebotomy and recombinant human erythropoietin, HAEMATOLOG, 85(8), 2000, pp. 865-867

Authors: Robson, KJH Merryweather-Clark, AT Pointon, JJ Shearman, JD Halsall, DJ Kelly, A Cox, TM Rosenberg, WM Howell, M Eccles, D Patch, C Fowler, AV Wallace, DF Camaschella, C Roetto, A Zecchina, G De Gobbi, M Gasparini, P Cadet, E Vandwalle, JL Capron, D Rochette, J Borot, N Demangel, C Dery, R Vinel, JP Pascal, JP Coppin, H Roth, MP

Citation: Kjh. Robson et al., Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience, BR J HAEM, 108(1), 2000, pp. 31-39