Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

34 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Genetics of atrioventricular canal defects.
Pugnaloni F, Digilio MC, Putotto C, De Luca E, Marino B, Versacci P. Pugnaloni F, et al. 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.
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: pugnaloni f. 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.
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: pugnaloni f. Genes (Basel). 2021 Jul 8;12(7):1047. doi: 10.3390/genes12071047. Genes (Basel). 2021. PMID: 34356063 Free PMC article. Review.
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: pugnaloni f. 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.
Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease.
Putotto C, Unolt M, Lambiase C, Marchetti F, Anaclerio S, Favoriti A, Tancredi G, Mastromoro G, Pugnaloni F, Liberati N, De Luca E, Tarani L, De Canditiis D, Caputo V, Bernardini L, Digilio MC, Marino B, Versacci P. Putotto C, et al. Among authors: pugnaloni f. Eur J Med Genet. 2023 Jan;66(1):104651. doi: 10.1016/j.ejmg.2022.104651. Epub 2022 Oct 28. Eur J Med Genet. 2023. PMID: 36404488
34 results