Disma Renda

Hepatocellular carcinoma in the thalassaemia syndromes

Caterina Borgna‐Pignatti, Gianluca Vergine, T. Lombardo et al. · British Journal of Haematology · 2003 · 175 citations

Pathology, Cirrhosis, Hepatobiliary Tumor +17

Oral supplements of vitamin E improve measures of oxidative stress in plasma and reduce oxidative damage to LDL and erythrocytes in β-thalassemia intermedia patients

Luisa Tesoriere, Daniele D’Arpa, Daniela Butera et al. · Free Radical Research · 2001 · 92 citations

Significance of borderline hemoglobin A2 values in an Italian population with a high prevalence of  -thalassemia

Antonino Giambona, Cristina Passarello, Margherita Vinciguerra et al. · Haematologica · 2008 · 71 citations · Full text

Immunohematology, Genetics, Genetic Epidemiology +20

Desensitization to hydroxycarbamide following long‐term treatment of thalassaemia intermedia as observed <i>in vivo</i> and in primary erythroid cultures from treated patients

Paolo Rigano, A. Pecoraro, Roberta Calzolari et al. · British Journal of Haematology · 2010 · 43 citations · Full text

The genetic heterogeneity of β-globin gene defects in Sicily reflects the historic population migrations of the island

Antonino Giambona, Margherita Vinciguerra, Monica Cannata et al. · Blood Cells Molecules and Diseases · 2011 · 36 citations

Genetic Analysis, β-Globin Gene Defects, Molecular Ecology +10