P. D. Michele

The polymorphisms −318C>T in the promoter and 49A>G in exon 1 of CTLA4 and the risk of aplastic anemia in a Caucasian population

A. Iolascon, M. Capasso, A. Pistorio, 2005, Bone Marrow Transplantation.

Homozygosis for (12) CA repeats in the first intron of the human IFN‐γ gene is significantly associated with the risk of aplastic anaemia in Caucasian population

A. Iolascon, M. Capasso, A. Pistorio, 2004, British journal of haematology.

Genetic polymorphism of NAD(P)H:quinone oxidoreductase is associated with an increased risk of infant acute lymphoblastic leukemia without MLL gene rearrangements

M. Valsecchi, G. Basso, M. Luciani, 2005, Leukemia.

Are genotypes of glutathione S-transferase superfamily a risk factor for childhood acute lymphoblastic leukemia? Results of an Italian case–control study

G. Basso, A. Biondi, R. Haupt, 2007, Leukemia.

Glutathione S-transferase polymorphisms and susceptibility to neuroblastoma

G. Tonini, L. Boni, R. Haupt, 2005, Pharmacogenetics and genomics.

Genotypes of the glutathione S-transferase superfamily do not correlate with outcome of childhood acute lymphoblastic leukemia

M. Valsecchi, G. Basso, A. Biondi, 2003, Leukemia.