Authors: Girelli, D Bozzini, C Zecchina, G Tinazzi, E Bosio, S Piperno, A Ramenghi, U Peters, J Levi, S Camaschella, C Corrocher, R

Citation: D. Girelli et al., Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome, BR J HAEM, 115(2), 2001, pp. 334-340

Authors: Camaschella, C Zecchina, G Lockitch, G Roetto, A Campanella, A Arosio, P Levi, S

Citation: C. Camaschella et al., A new mutation (G51C) in the iron-responsive element (IRE) of L-ferritin associated with hyperferritinaemia-cataract syndrome decreases the binding affinity of the mutated IRE for iron-regulatory proteins, BR J HAEM, 108(3), 2000, pp. 480-482

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

Authors: Longo, F Zecchina, G Sbaiz, L Fischer, R Piga, A Camaschella, C

Citation: F. Longo et al., The influence of hemochromatosis mutations on iron overload of thalassemiamajor, HAEMATOLOG, 84(9), 1999, pp. 799-803

Authors: Cicilano, M Zecchina, G Roetto, A Bosio, S Infelise, V Stefani, S Mazza, U Camaschella, C

Citation: M. Cicilano et al., Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndrome, HAEMATOLOG, 84(6), 1999, pp. 489-492

Authors: Bosio, S Zecchina, G Cicilano, M Roetto, A Saito, AM Camaschella, C

Citation: S. Bosio et al., Variation in the phenotypic expression of C282Y hemochromatosis in an Italian family, HAEMATOLOG, 84(2), 1999, pp. 184-185