CACP syndrome: identification of five novel mutations and of the first case of UPD in the largest European cohort

Por Ciullini Mannurita, Sara, Vignoli, Marina, Bianchi, Lucia, Kondi, Anuela, Gerloni, Valeria, Breda, Luciana, ten Cate, Rebecca, Alessio, Maria, Ravelli, Angelo, Falcini, Fernanda, Gambineri, Eleonora
Publicado em 2014

Clinical, Immunological, and Molecular Heterogeneity of 173 Patients With the Phenotype of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome

Por Gambineri, Eleonora, Ciullini Mannurita, Sara, Hagin, David, Vignoli, Marina, Anover-Sombke, Stephanie, DeBoer, Stacey, Segundo, Gesmar R. S., Allenspach, Eric J., Favre, Claudio, Ochs, Hans D., Torgerson, Troy R.
Publicado no Front Immunol (2018)

Gut immune reconstitution in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome after hematopoietic stem cell transplantation

Por Gambineri, Eleonora, Ciullini Mannurita, Sara, Robertson, Helen, Vignoli, Marina, Haugk, Beate, Lionetti, Paolo, Hambleton, Sophie, Barge, Dawn, Gennery, Andrew R., Slatter, Mary, Nademi, Zohreh, Flood, Terence J., Jackson, Anthony, Abinun, Mario, Cant, Andrew J.
Publicado no J Allergy Clin Immunol (2015)

Demethylation analysis of the FOXP3 locus shows quantitative defects of regulatory T cells in IPEX-like syndrome

Por Barzaghi, F., Passerini, L., Gambineri, E., Ciullini Mannurita, S., Cornu, T., Kang, E.S., Choe, Y.H., Cancrini, C., Corrente, S., Ciccocioppo, R., Cecconi, M., Zuin, G., Discepolo, V., Sartirana, C., Schmidtko, J., Ikinciogullari, A., Ambrosi, A., Roncarolo, M.G., Olek, S., Bacchetta, R.
Publicado em 2012