Silvia Giliani
Angelo Nocivelli Institute of Molecular Medicine and Department of Pediatrics
University of Brescia
Brescia
Italy
Name/email consistency: high
- Omenn syndrome in an infant with IL7RA gene mutation. Giliani, S., Bonfim, C., de Saint Basile, G., Lanzi, G., Brousse, N., Koliski, A., Malvezzi, M., Fischer, A., Notarangelo, L.D., Le Deist, F. J. Pediatr. (2006)
- Interleukin-7 receptor alpha (IL-7Ralpha) deficiency: cellular and molecular bases. Analysis of clinical, immunological, and molecular features in 16 novel patients. Giliani, S., Mori, L., de Saint Basile, G., Le Deist, F., Rodriguez-Perez, C., Forino, C., Mazzolari, E., Dupuis, S., Elhasid, R., Kessel, A., Galambrun, C., Gil, J., Fischer, A., Etzioni, A., Notarangelo, L.D. Immunol. Rev. (2005)
- Cytokine-mediated signalling and early defects in lymphoid development. Giliani, S., Mella, P., Savoldi, G., Mazzolari, E. Curr. Opin. Allergy. Clin. Immunol (2005)
- Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis. Giliani, S., Fiorini, M., Mella, P., Candotti, F., Schumacher, R.F., Wengler, G.S., Lalatta, F., Fasth, A., Badolato, R., Ugazio, A.G., Albertini, A., Notarangelo, L.D. Prenat. Diagn. (1999)