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Alcoholism, Clinical and Experimental Research|December 1, 1995
Carbohydrate-deficient transferrin in alcohol and nonalcohol abusers with liver diseaseM Meregalli, V Giacomini, S Lino, et al.
European Journal of Clinical Investigation|March 12, 2002
Oxidative status and malondialdehyde in beta-thalassaemia patientsGiuliana Cighetti, L Duca, L Bortone, et al.
Annals of the New York Academy of Sciences|July 21, 1998
Butyrate trialsM D Cappellini, G Graziadei, L Ciceri, et al.
British Journal of Haematology|December 21, 2000
Venous thromboembolism and hypercoagulability in splenectomized patients with thalassaemia intermediaM D Cappellini, L Robbiolo, B M Bottasso, et al.
Blood|May 1, 1996
Multiple G6PD mutations are associated with a clinical and biochemical phenotype similar to that of G6PD MediterraneanM D Cappellini, F Martinez di Montemuros, G De Bellis, et al.
British Journal of Haematology|March 1, 1986
Feasibility of prenatal diagnosis of beta thalassaemia by DNA polymorphisms in an Italian populationJ S Wainscoat, S Work, M Sampietro, et al.
British Journal of Haematology|December 31, 1997
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiencyM Sampietro, L Lupica, L Perrero, et al.
British Journal of Haematology|July 1, 1986
Alpha thalassaemia in an Italian populationC Velati, M Sampietro, M Biassoni, et al.
British Journal of Haematology|March 23, 1999
Metabolic indicators of oxidative stress correlate with haemichrome attachment to membrane, band 3 aggregation and erythrophagocytosis in beta-thalassaemia intermediaM D Cappellini, D Tavazzi, L Duca, et al.
European Journal of Clinical Investigation|March 1, 1993
Alternative splicing of human G6PD messenger RNA in K562 cells but not in cultured erythroblastsM D Cappellini, D Tavazzi, F Martinez di Montemuros, et al.
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