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Case Report: Atypical Manifestations Associated With FOXP3 Mutations. The "Fil Rouge" of Treg Between IPEX Features and Other Clinical Entities?
Gentile M, Miano M, Terranova P, Giardino S, Faraci M, Pierri F, Drago E, Verzola D, Ghiggeri G, Verrina E, Angeletti A, Cafferata B, Grossi A, Ceccherini I, Caridi G, Lugani F, Nescis L, Fiaccadori E, Lanino L, Fenoglio D, La Porta E. Gentile M, et al. Among authors: lugani f. Front Immunol. 2022 Apr 11;13:854749. doi: 10.3389/fimmu.2022.854749. eCollection 2022. Front Immunol. 2022. PMID: 35479070 Free PMC article.
Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy.
Caridi G, Lugani F, Dagnino M, Gigante M, Iolascon A, Falco M, Graziano C, Benetti E, Dugo M, Del Prete D, Granata A, Borracelli D, Moggia E, Quaglia M, Rinaldi R, Gesualdo L, Ghiggeri GM. Caridi G, et al. Among authors: lugani f. Nephrol Dial Transplant. 2014 Sep;29 Suppl 4:iv80-6. doi: 10.1093/ndt/gfu071. Nephrol Dial Transplant. 2014. PMID: 25165188
Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia.
Minchiotti L, Caridi G, Campagnoli M, Lugani F, Galliano M, Kragh-Hansen U. Minchiotti L, et al. Among authors: lugani f. Front Genet. 2019 Apr 17;10:336. doi: 10.3389/fgene.2019.00336. eCollection 2019. Front Genet. 2019. PMID: 31057599 Free PMC article. Review.
88 results