Authors: Garozzo, G Distefano, R Miceli, A Bonomo, P

Citation: G. Garozzo et al., Detection of ICAM-1, ICAM-2, ICAM-3, PECAM-1 and VCAM-1, evaluation of hypercoagulable state and platelet aggregation in hemoglobinopathy patients with erythroblasts, HAEMATOLOG, 86(7), 2001, pp. 778-779

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: 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: Garozzo, G Disca, S Fidone, C Bonomo, P

Citation: G. Garozzo et al., Azoospermia in a patient with sickle cell disease treated with hydroxyurea, HAEMATOLOG, 85(11), 2000, pp. 1216-1218

Authors: Camaschella, C Fargion, S Sampietro, M Roetto, A Bosio, S Garozzo, G Arosio, C Piperno, A

Citation: C. Camaschella et al., Inherited HFE-unrelated hemochromatosis in Italian families, HEPATOLOGY, 29(5), 1999, pp. 1563-1564