Peripheral blood cells from children with RASopathies show enhanced spontaneous colonies growth in vitro and hyperactive RAS signaling

por Gaipa, G, Bugarin, C, Cianci, P, Sarno, J, Bonaccorso, P, Biondi, A, Selicorni, A
Publicado 2015

Cornelia de Lange Syndrome: NIPBL haploinsufficiency downregulates canonical Wnt pathway in zebrafish embryos and patients fibroblasts

por Pistocchi, A, Fazio, G, Cereda, A, Ferrari, L, Bettini, L R, Messina, G, Cotelli, F, Biondi, A, Selicorni, A, Massa, V
Publicado 2013

Daily life changes and adaptations investigated in 154 families with a child suffering from a rare disability at a public centre for rare diseases in Northern Italy

por Silibello, G., Vizziello, P., Gallucci, M., Selicorni, A., Milani, D., Ajmone, P. F., Rigamonti, C., De Stefano, S., Bedeschi, M. F., Lalatta, Faustina
Publicado 2016

Drooling outcome measures in paediatric disability: a systematic review

por Sforza, E., Onesimo, R., Leoni, C., Giorgio, V., Proli, F., Notaro, F., Kuczynska, E. M., Cerchiari, A., Selicorni, A., Rigante, D., Zampino, G.
Publicado 2022

Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders

por Fontana, L., Bedeschi, M. F., Maitz, S., Cereda, A., Faré, C., Motta, S., Seresini, A., D’Ursi, P., Orro, A., Pecile, V., Calvello, M., Selicorni, A., Lalatta, F., Milani, D., Sirchia, S. M., Miozzo, M., Tabano, S.
Publicado 2018

In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS)

por Ranieri, C., Di Tommaso, S., Loconte, D. C., Grossi, V., Sanese, P., Bagnulo, R., Susca, F. C., Forte, G., Peserico, A., De Luisi, A., Bartuli, A., Selicorni, A., Melis, D., Lerone, M., Praticò, A. D., Abbadessa, G., Yu, Y., Schwartz, B., Ruggieri, Martino, Simone, Cristiano, Resta, Nicoletta
Publicado 2018