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

Year Number of Results
1997 1
2002 1
2004 3
2005 2
2006 2
2007 1
2008 1
2009 3
2010 6
2011 10
2012 6
2013 3
2014 1
2015 5
2017 4
2018 9
2019 9
2020 10
2021 13
2022 11
2023 3
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86 results
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Page 1
Clinical Manifestations of 22q11.2 Deletion Syndrome.
Cirillo A, Lioncino M, Maratea A, Passariello A, Fusco A, Fratta F, Monda E, Caiazza M, Signore G, Esposito A, Baban A, Versacci P, Putotto C, Marino B, Pignata C, Cirillo E, Giardino G, Sarubbi B, Limongelli G, Russo MG. Cirillo A, et al. Among authors: versacci p. Heart Fail Clin. 2022 Jan;18(1):155-164. doi: 10.1016/j.hfc.2021.07.009. Epub 2021 Oct 25. Heart Fail Clin. 2022. PMID: 34776076 Review.
Cardiovascular disease in Down syndrome.
Versacci P, Di Carlo D, Digilio MC, Marino B. Versacci P, et al. Curr Opin Pediatr. 2018 Oct;30(5):616-622. doi: 10.1097/MOP.0000000000000661. Curr Opin Pediatr. 2018. PMID: 30015688 Review.
Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients.
Maioli M, Gnoli M, Boarini M, Tremosini M, Zambrano A, Pedrini E, Mordenti M, Corsini S, D'Eufemia P, Versacci P, Celli M, Sangiorgi L. Maioli M, et al. Among authors: versacci p. Eur J Hum Genet. 2019 Jul;27(7):1090-1100. doi: 10.1038/s41431-019-0373-x. Epub 2019 Mar 18. Eur J Hum Genet. 2019. PMID: 30886339 Free PMC article. Clinical Trial.
Congenital heart defects in the recurrent 2q13 deletion syndrome.
Digilio MC, Dentici ML, Loddo S, Laino L, Calcagni G, Genovese S, Capolino R, Bottillo I, Calvieri G, Dallapiccola B, Marino B, Novelli A, Versacci P. Digilio MC, et al. Among authors: versacci p. Eur J Med Genet. 2022 Jan;65(1):104381. doi: 10.1016/j.ejmg.2021.104381. Epub 2021 Nov 8. Eur J Med Genet. 2022. PMID: 34763108 Review.
The heart in RASopathies.
Delogu AB, Limongelli G, Versacci P, Adorisio R, Kaski JP, Blandino R, Maiolo S, Monda E, Putotto C, De Rosa G, Chatfield KC, Gelb BD, Calcagni G. Delogu AB, et al. Among authors: versacci p. Am J Med Genet C Semin Med Genet. 2022 Dec;190(4):440-451. doi: 10.1002/ajmg.c.32014. Epub 2022 Nov 21. Am J Med Genet C Semin Med Genet. 2022. PMID: 36408797 Review.
Genetics of atrioventricular canal defects.
Pugnaloni F, Digilio MC, Putotto C, De Luca E, Marino B, Versacci P. Pugnaloni F, et al. Among authors: versacci p. Ital J Pediatr. 2020 May 13;46(1):61. doi: 10.1186/s13052-020-00825-4. Ital J Pediatr. 2020. PMID: 32404184 Free PMC article. Review.
When to test fetuses for RASopathies? Proposition from a systematic analysis of 352 multicenter cases and a postnatal cohort.
Scott A, Di Giosaffatte N, Pinna V, Daniele P, Corno S, D'Ambrosio V, Andreucci E, Marozza A, Sirchia F, Tortora G, Mangiameli D, Di Marco C, Romagnoli M, Donati I, Zonta A, Grosso E, Naretto VG, Mastromoro G, Versacci P, Pantaleoni F, Radio FC, Mazza T, Damante G, Papi L, Mattina T, Giancotti A, Pizzuti A, Laberge AM, Tartaglia M, Delrue MA, De Luca A. Scott A, et al. Among authors: versacci p. Genet Med. 2021 Jun;23(6):1116-1124. doi: 10.1038/s41436-020-01093-7. Epub 2021 Feb 10. Genet Med. 2021. PMID: 33568805 Free article.
Nerve Growth Factor, Stress and Diseases.
Ceci FM, Ferraguti G, Petrella C, Greco A, Tirassa P, Iannitelli A, Ralli M, Vitali M, Ceccanti M, Chaldakov GN, Versacci P, Fiore M. Ceci FM, et al. Among authors: versacci p. Curr Med Chem. 2021;28(15):2943-2959. doi: 10.2174/0929867327999200818111654. Curr Med Chem. 2021. PMID: 32811396 Review.
Neonatal Marfan Syndrome by Inherited Mutation.
Mastromoro G, Guida V, Cellitti R, Cardilli V, De Luca A, Pizzuti A, Versacci P. Mastromoro G, et al. Among authors: versacci p. Indian J Pediatr. 2021 Feb;88(2):176-177. doi: 10.1007/s12098-020-03411-y. Epub 2020 Jun 17. Indian J Pediatr. 2021. PMID: 32557139 No abstract available.
Cardiac Defects and Genetic Syndromes: Old Uncertainties and New Insights.
Calcagni G, Pugnaloni F, Digilio MC, Unolt M, Putotto C, Niceta M, Baban A, Piceci Sparascio F, Drago F, De Luca A, Tartaglia M, Marino B, Versacci P. Calcagni G, et al. Among authors: versacci p. Genes (Basel). 2021 Jul 8;12(7):1047. doi: 10.3390/genes12071047. Genes (Basel). 2021. PMID: 34356063 Free PMC article. Review.
86 results