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Page 1
RASopathy Syndrome: Do Not Overlook Mitral Valve Anomalies!
Calcagni G, Maiolo S, Marino B, Putotto C. Calcagni G, et al. JACC Case Rep. 2024 Oct 2;29(19):102604. doi: 10.1016/j.jaccas.2024.102604. eCollection 2024 Oct 2. JACC Case Rep. 2024. PMID: 39484325 Free PMC article. No abstract available.
Some Isolated Cardiac Malformations Can Be Related to Laterality Defects.
Versacci P, Pugnaloni F, Digilio MC, Putotto C, Unolt M, Calcagni G, Baban A, Marino B. Versacci P, et al. Among authors: calcagni g. J Cardiovasc Dev Dis. 2018 May 2;5(2):24. doi: 10.3390/jcdd5020024. J Cardiovasc Dev Dis. 2018. PMID: 29724030 Free PMC article. Review.
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice.
Mastromoro G, Calcagni G, Versacci P, Putotto C, Chinali M, Lambiase C, Unolt M, Pelliccione E, Anaclerio S, Caprio C, Cioffi S, Bilio M, Baban A, Drago F, Digilio MC, Marino B, Baldini A. Mastromoro G, et al. Among authors: calcagni g. PLoS One. 2019 Apr 1;14(4):e0211170. doi: 10.1371/journal.pone.0211170. eCollection 2019. PLoS One. 2019. PMID: 30933971 Free PMC article.
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. Genes (Basel). 2021 Jul 8;12(7):1047. doi: 10.3390/genes12071047. Genes (Basel). 2021. PMID: 34356063 Free PMC article. Review.
Congenital heart defects in molecularly confirmed KBG syndrome patients.
Digilio MC, Calcagni G, Gnazzo M, Versacci P, Dentici ML, Capolino R, Sinibaldi L, Baban A, Putotto C, Alfieri P, Unolt M, Lepri FR, Alesi V, Genovese S, Novelli A, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: calcagni g. Am J Med Genet A. 2022 Apr;188(4):1149-1159. doi: 10.1002/ajmg.a.62632. Epub 2021 Dec 31. Am J Med Genet A. 2022. PMID: 34971082
Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes-A report of 74 cases with systematic review of the literature.
Mastromoro G, Calcagni G, Vignaroli W, Anaclerio S, Pugnaloni F, Rinelli G, Secinaro A, Bordonaro V, Putotto C, Unolt M, Digilio MC, Marino B, Versacci P. Mastromoro G, et al. Among authors: calcagni g. Am J Med Genet A. 2022 Aug;188(8):2351-2359. doi: 10.1002/ajmg.a.62763. Epub 2022 May 2. Am J Med Genet A. 2022. PMID: 35491976 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: calcagni g. 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.
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