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Hospitalization for bronchiolitis in children aged ≤ 1year, Southern Italy, year 2021: need for new preventive strategies?
Baldassarre ME, Loconsole D, Centrone F, Caselli D, Martire B, Quartulli L, Acquafredda A, D'Amato G, Maffei G, Latorre G, Riganti A, Di Noia M, Chironna M, Laforgia N. Baldassarre ME, et al. Among authors: laforgia n. Ital J Pediatr. 2023 Jun 6;49(1):66. doi: 10.1186/s13052-023-01455-2. Ital J Pediatr. 2023. PMID: 37280662 Free PMC article.
Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome.
Niceta M, Margiotti K, Digilio MC, Guida V, Bruselles A, Pizzi S, Ferraris A, Memo L, Laforgia N, Dentici ML, Consoli F, Torrente I, Ruiz-Perez VL, Dallapiccola B, Marino B, De Luca A, Tartaglia M. Niceta M, et al. Among authors: laforgia n. Clin Genet. 2018 Mar;93(3):632-639. doi: 10.1111/cge.13128. Epub 2018 Jan 24. Clin Genet. 2018. PMID: 28857138
Lingual laser frenotomy in newborns with ankyloglossia: a prospective cohort study.
Dell'Olio F, Baldassarre ME, Russo FG, Schettini F, Siciliani RA, Mezzapesa PP, Tempesta A, Laforgia N, Favia G, Limongelli L. Dell'Olio F, et al. Among authors: laforgia n. Ital J Pediatr. 2022 Sep 5;48(1):163. doi: 10.1186/s13052-022-01357-9. Ital J Pediatr. 2022. PMID: 36064609 Free PMC article.
A Rare Case of Severe Congenital RYR1-Associated Myopathy.
Laforgia N, Capozza M, De Cosmo L, Di Mauro A, Baldassarre ME, Mercadante F, Torella AL, Nigro V, Resta N. Laforgia N, et al. Case Rep Genet. 2018 Aug 1;2018:6184185. doi: 10.1155/2018/6184185. eCollection 2018. Case Rep Genet. 2018. PMID: 30155320 Free PMC article.
189 results