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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 2
2009 2
2010 2
2012 1
2013 3
2014 3
2015 1
2016 1
2017 1
2018 4
2019 1
2020 12
2021 5
2022 14
2023 3
2024 1

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Page 1
NFIA haploinsufficiency: case series and literature review.
Dini G, Verrotti A, Gorello P, Soliani L, Cordelli DM, Antona V, Mencarelli A, Colavito D, Prontera P. Dini G, et al. Among authors: antona v. Front Pediatr. 2023 Oct 17;11:1292654. doi: 10.3389/fped.2023.1292654. eCollection 2023. Front Pediatr. 2023. PMID: 37915986 Free PMC article.
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.
Picketts D, Mirzaa G, Yan K, Relator R, Timpano S, Yalcin B, Collins S, Ziegler A, Pao E, Oyama N, Brischoux-Boucher E, Piard J, Monaghan K, Sacoto MG, Dobyns W, Park K, Fernández-Mayoralas D, Fernández-Jaén A, Jayakar P, Brusco A, Antona V, Giorgio E, Kvarnung M, Isidor B, Conrad S, Cogné B, Deb W, Stuurman KE, Sterbova K, Smal N, Weckhuysen S, Oegema R, Innes M, Latsko M, Ben-Omran T, Yeh R, Kruer M, Bakhtiari S, Papavasiliou A, Moutton S, Nambot S, Chanprasert S, Paolucci S, Miller K, Burton B, Kim K, O'Heir E, Bruwer Z, Donald K, Kleefstra T, Goldstein A, Angle B, Bontempo K, Miny P, Joset P, Demurger F, Hobson E, Pang L, Carpenter L, Li D, Bonneau D, Sadikovic B. Picketts D, et al. Among authors: antona v. Res Sq [Preprint]. 2023 Sep 29:rs.3.rs-3317938. doi: 10.21203/rs.3.rs-3317938/v1. Res Sq. 2023. PMID: 37841849 Free PMC article. Preprint.
Genetic Basis of Posterior Urethral Valves Inheritance.
Chiaramonte C, Bommarito D, Zambaiti E, Antona V, Li Voti G. Chiaramonte C, et al. Among authors: antona v. Urology. 2016 Sep;95:175-9. doi: 10.1016/j.urology.2016.05.043. Epub 2016 May 31. Urology. 2016. PMID: 27261184 Review.
Recognizable neonatal clinical features of aplasia cutis congenita.
Schierz IAM, Giuffrè M, Del Vecchio A, Antona V, Corsello G, Piro E. Schierz IAM, et al. Among authors: antona v. Ital J Pediatr. 2020 Feb 18;46(1):25. doi: 10.1186/s13052-020-0789-5. Ital J Pediatr. 2020. PMID: 32070410 Free PMC article.
A novel NF1 mutation in a pediatric patient with renal artery aneurysm.
Chillura I, Restivo GA, Callari S, Cibella S, D'Alessandro MM, Corrado C, Vallone M, Antona V, Corsello G. Chillura I, et al. Among authors: antona v. Ital J Pediatr. 2022 Nov 21;48(1):186. doi: 10.1186/s13052-022-01382-8. Ital J Pediatr. 2022. PMID: 36411470 Free PMC article.
50 results