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Page 1
Drooling outcome measures in paediatric disability: a systematic review.
Sforza E, Onesimo R, Leoni C, Giorgio V, Proli F, Notaro F, Kuczynska EM, Cerchiari A, Selicorni A, Rigante D, Zampino G. Sforza E, et al. Among authors: selicorni a. Eur J Pediatr. 2022 Jul;181(7):2575-2592. doi: 10.1007/s00431-022-04460-5. Epub 2022 Apr 20. Eur J Pediatr. 2022. PMID: 35441248 Free PMC article. Review.
[Follow-up of the neonate with malformation syndrome].
Memo L, Selicorni A, Zampino G. Memo L, et al. Among authors: selicorni a. Minerva Pediatr. 2007 Oct;59(5):503-6. Minerva Pediatr. 2007. PMID: 17947891 Italian. No abstract available.
Visual function in Noonan and LEOPARD syndrome.
Alfieri P, Cesarini L, Zampino G, Pantaleoni F, Selicorni A, Salerni A, Vasta I, Cerutti M, Dickmann A, Colitto F, Staccioli S, Leoni C, Ricci D, Brogna C, Tartaglia M, Mercuri E. Alfieri P, et al. Among authors: selicorni a. Neuropediatrics. 2008 Dec;39(6):335-40. doi: 10.1055/s-0029-1216354. Epub 2009 Jun 30. Neuropediatrics. 2008. PMID: 19568997
Behavioral profile in RASopathies.
Alfieri P, Piccini G, Caciolo C, Perrino F, Gambardella ML, Mallardi M, Cesarini L, Leoni C, Leone D, Fossati C, Selicorni A, Digilio MC, Tartaglia M, Mercuri E, Zampino G, Vicari S. Alfieri P, et al. Among authors: selicorni a. Am J Med Genet A. 2014 Apr;164A(4):934-42. doi: 10.1002/ajmg.a.36374. Epub 2014 Jan 23. Am J Med Genet A. 2014. PMID: 24458522
Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, management and follow-up of the syndrome.
Mussa A, Di Candia S, Russo S, Catania S, De Pellegrin M, Di Luzio L, Ferrari M, Tortora C, Meazzini MC, Brusati R, Milani D, Zampino G, Montirosso R, Riccio A, Selicorni A, Cocchi G, Ferrero GB. Mussa A, et al. Among authors: selicorni a. Eur J Med Genet. 2016 Jan;59(1):52-64. doi: 10.1016/j.ejmg.2015.11.008. Epub 2015 Nov 22. Eur J Med Genet. 2016. PMID: 26592461 Review.
Children with special health care needs attending emergency department in Italy: analysis of 3479 cases.
Cianci P, D'Apolito V, Moretti A, Barbagallo M, Paci S, Carbone MT, Lubrano R, Urbino A, Dionisi Vici C, Memo L, Zampino G, La Marca G, Villani A, Corsello G, Selicorni A; Italian Society of Pediatrics (SIP); Italian Society of Pediatric Genetic Diseases and Congenital Disabilities (SIMGePed) the Italian Society of Pediatric Emergency Medicine (SIMEUP); Italian Society For The Study Of Inborn Metabolic Disorders And Newborn Screening (SIMMENS) and Members of Italian Network. Cianci P, et al. Among authors: selicorni a. Ital J Pediatr. 2020 Nov 23;46(1):173. doi: 10.1186/s13052-020-00937-x. Ital J Pediatr. 2020. PMID: 33228805 Free PMC article.
ANKRD11 variants: KBG syndrome and beyond.
Parenti I, Mallozzi MB, Hüning I, Gervasini C, Kuechler A, Agolini E, Albrecht B, Baquero-Montoya C, Bohring A, Bramswig NC, Busche A, Dalski A, Guo Y, Hanker B, Hellenbroich Y, Horn D, Innes AM, Leoni C, Li YR, Lynch SA, Mariani M, Medne L, Mikat B, Milani D, Onesimo R, Ortiz-Gonzalez X, Prott EC, Reutter H, Rossier E, Selicorni A, Wieacker P, Wilkens A, Wieczorek D, Zackai EH, Zampino G, Zirn B, Hakonarson H, Deardorff MA, Gillessen-Kaesbach G, Kaiser FJ. Parenti I, et al. Among authors: selicorni a. Clin Genet. 2021 Aug;100(2):187-200. doi: 10.1111/cge.13977. Epub 2021 May 14. Clin Genet. 2021. PMID: 33955014 Free article.
262 results