KULLMANN GAIA ALESSANDRA

Faraguna, M., Crescitelli, V., Bonanomi, S., Kullmann, G., Boffi, M., Pretese, R., et al. (2026). A comprehensive study on the effect of alglucosidase alpha and immunomodulation on survival, motor and cardiac outcome, creatine kinase and antibody titers in classic infantile Pompe disease: the Monza experience. CURRENT OPINION IN IMMUNOLOGY, 99(April 2026) [10.1016/j.coi.2026.102725]. Detail

Pasca, L., Politano, D., Cavallini, A., Panzeri, E., Vigone, M., Baldoli, C., et al. (2024). A Novel De novo Heterozygous Mutation in the SON Gene Associated with Septo-optic Dysplasia: A New Phenotype. NEUROPEDIATRICS, 55(3), 191-195 [10.1055/a-2114-4387]. Detail

Faraguna, M., Musto, F., Crescitelli, V., Iascone, M., Spaccini, L., Tonduti, D., et al. (2022). Mucopolysaccharidosis-Plus Syndrome, a Rapidly Progressive Disease: Favorable Impact of a Very Prolonged Steroid Treatment on the Clinical Course in a Child. GENES, 13(3) [10.3390/genes13030442]. Detail

Lambicchi, L., Locatelli, A., Incerti, M., Matallo, F., Bonati, F., Kullmann, G., et al. (2018). Is neonatal asphyxia preventable?. Intervento presentato a: Annual Meeting 2018 Society for Maternal Fetal Medicine, Dallas. Detail

Cereda, A., Mariani, M., Rebora, P., Sajeva, A., Ajmone, P., Gervasini, C., et al. (2016). A new prognostic index of severity of intellectual disabilities in Cornelia de Lange syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS. PART C, SEMINARS IN MEDICAL GENETICS, 172(2), 179-189 [10.1002/ajmg.c.31494]. Detail