V. Servedio

发表

K-CL co-transport plays an important role in normal and β thalassemic erythropoiesis

A. Iolascon, S. Alper, M. Cappellini, 2007, Haematologica.

Hereditary Thrombocytopenia due to Reduced Platelet Production

A. Savoia, A. Iolascon, P. Strippoli, 2000, Thrombosis and Haemostasis.

Spectrum of UGT1A1 mutations in Crigler‐Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype‐phenotype correlation

S. Perrotta, F. Torricelli, A. Iolascon, 2005, Human mutation.

Osteoporosis in β‐thalassaemia major patients: analysis of the genetic background

S. Perrotta, P. Gasparini, A. Iolascon, 2000, British journal of haematology.

Osteoporosis in beta-thalassaemia major patients: analysis of the genetic background.

S. Perrotta, P. Gasparini, A. Iolascon, 2000 .

MICROCYTIC ANEMIA AND HEPATIC IRON OVERLOAD IN A CHILD WITH COMPOUND HETEROZYGOUS MUTATIONS IN DMT 1

A. Iolascon, A. Piga, C. Camaschella, 2005 .

Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II).

S. Perrotta, A. Iolascon, E. D. del Giudice, 2000, The Journal of pediatrics.

Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2).

A. Iolascon, A. Piga, C. Camaschella, 2006, Blood.

Two regions of deletion in 9p22- p24 in neuroblastoma are frequently observed in favorable tumors.

G. Tonini, A. Iolascon, L. Longo, 2002, Cancer genetics and cytogenetics.

Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?

H. Heimpel, S. Perrotta, P. Gasparini, 2000, Haematologica.

Genes transcriptionally modulated by interferon alpha2a correlate with the cytokine activity.

S. Volinia, P. Gasparini, A. Iolascon, 2004, Haematologica.

Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia.

A. Iolascon, L. De Falco, P. Vajro, 2007, Haematologica.