Achille Iolascon
Genetica Medica
Dipartimento di Biochimica e Biotecnologie Mediche
Università Federico II
Naples
Italy
Name/email consistency: high
- Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis. Iolascon, A., De Falco, L., Beaumont, C. Haematologica (2009)
- Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2). Iolascon, A., d'Apolito, M., Servedio, V., Cimmino, F., Piga, A., Camaschella, C. Blood (2006)
- Congenital nephrotic syndrome of Finnish type: detection of new nephrin mutations and prenatal diagnosis in an Italian family. Gigante, M., Greco, P., Defazio, V., Lucci, M., Margaglione, M., Gesualdo, L., Iolascon, A. Prenat. Diagn. (2005)