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Serratia marcescens osteomyelitis in a newborn with chronic granulomatous disease.
Salfa I, Cantarutti N, Angelino G, Di Matteo G, Capo V, Farinelli G, Cancrini C, Aiuti A, Palma P, Finocchi A. Salfa I, et al. Among authors: angelino g. Pediatr Infect Dis J. 2013 Aug;32(8):926. doi: 10.1097/INF.0b013e31828f682a. Pediatr Infect Dis J. 2013. PMID: 23518820 No abstract available.
Late-onset combined immune deficiency due to LIGIV mutations in a 12-year-old patient.
Cifaldi C, Angelino G, Chiriaco M, Di Cesare S, Claps A, Serafinelli J, Rossi P, Antoccia A, Di Matteo G, Cancrini C, De Villartay JP, Finocchi A. Cifaldi C, et al. Among authors: angelino g. Pediatr Allergy Immunol. 2017 Mar;28(2):203-206. doi: 10.1111/pai.12684. Pediatr Allergy Immunol. 2017. PMID: 27893162 No abstract available.
Immunodeficiency in Vici syndrome: a heterogeneous phenotype.
Finocchi A, Angelino G, Cantarutti N, Corbari M, Bevivino E, Cascioli S, Randisi F, Bertini E, Dionisi-Vici C. Finocchi A, et al. Among authors: angelino g. Am J Med Genet A. 2012 Feb;158A(2):434-9. doi: 10.1002/ajmg.a.34244. Epub 2011 Sep 30. Am J Med Genet A. 2012. PMID: 21965116
41 results