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Cow's milk protein allergy in children: a practical guide.
Caffarelli C, Baldi F, Bendandi B, Calzone L, Marani M, Pasquinelli P; EWGPAG. Caffarelli C, et al. Ital J Pediatr. 2010 Jan 15;36:5. doi: 10.1186/1824-7288-36-5. Ital J Pediatr. 2010. PMID: 20205781 Free PMC article. Review.
Healthcare migration in Italian paediatric haematology-oncology centres belonging to AIEOP.
Rondelli R, Belotti T, Masetti R, Locatelli F, Massimino M, Biffi A, Dufour C, Fagioli F, Menna G, Biondi A, Favre C, Zecca M, Santoro N, Russo G, Perrotta S, Pession A, Prete A. Rondelli R, et al. Among authors: menna g. Ital J Pediatr. 2024 Mar 7;50(1):44. doi: 10.1186/s13052-024-01620-1. Ital J Pediatr. 2024. PMID: 38454431 Free PMC article.
Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22.
Melis D, Genesio R, Cappuccio G, MariaGinocchio V, Casa RD, Menna G, Buffardi S, Poggi V, Leszle A, Imperati F, Carella M, Izzo A, Del Giudice E, Nitsch L, Andria G. Melis D, et al. Among authors: menna g. Am J Med Genet A. 2011 Jul;155A(7):1697-705. doi: 10.1002/ajmg.a.33976. Epub 2011 Jun 10. Am J Med Genet A. 2011. PMID: 21671372
Clinical features and follow-up in patients with 22q11.2 deletion syndrome.
Cancrini C, Puliafito P, Digilio MC, Soresina A, Martino S, Rondelli R, Consolini R, Ruga EM, Cardinale F, Finocchi A, Romiti ML, Martire B, Bacchetta R, Albano V, Carotti A, Specchia F, Montin D, Cirillo E, Cocchi G, Trizzino A, Bossi G, Milanesi O, Azzari C, Corsello G, Pignata C, Aiuti A, Pietrogrande MC, Marino B, Ugazio AG, Plebani A, Rossi P; Italian Network for Primary Immunodeficiencies. Cancrini C, et al. J Pediatr. 2014 Jun;164(6):1475-80.e2. doi: 10.1016/j.jpeds.2014.01.056. Epub 2014 Mar 20. J Pediatr. 2014. PMID: 24657119
159 results