Delogu AB - Search Results

1

Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness.

Sinibaldi L, Garone G, Mandarino A, Iarossi G, Chioma L, Dentici ML, Merla G, Agolini E, Micalizzi A, Mancini C, Niceta M, Macchiaiolo M, Diodato D, Onesimo R, Blandino R, Delogu AB, De Rosa G, Trevisan V, Iademarco M, Zampino G, Tartaglia M, Novelli A, Bartuli A, Digilio MC, Calcagni G. Sinibaldi L, et al. Among authors: delogu ab. Clin Genet. 2023 Nov;104(5):528-541. doi: 10.1111/cge.14404. Epub 2023 Jul 17. Clin Genet. 2023. PMID: 37455656

2

Smith Magenis syndrome: First case of congenital heart defect in a patient with Rai1 mutation.

Onesimo R, Delogu AB, Blandino R, Leoni C, Rosati J, Zollino M, Zampino G. Onesimo R, et al. Among authors: delogu ab. Am J Med Genet A. 2022 Jul;188(7):2184-2186. doi: 10.1002/ajmg.a.62740. Epub 2022 Apr 4. Am J Med Genet A. 2022. PMID: 35373511

3

Smith-Magenis syndrome: Report of morphological and new functional cardiac findings with review of the literature.

Onesimo R, Versacci P, Delogu AB, De Rosa G, Pugnaloni F, Blandino R, Leoni C, Calcagni G, Digilio MC, Zollino M, Marino B, Zampino G. Onesimo R, et al. Among authors: delogu ab. Am J Med Genet A. 2021 Jul;185(7):2003-2011. doi: 10.1002/ajmg.a.62196. Epub 2021 Apr 3. Am J Med Genet A. 2021. PMID: 33811726

4

Genotype-cardiac phenotype correlations in a large single-center cohort of patients affected by RASopathies: Clinical implications and literature review.

Leoni C, Blandino R, Delogu AB, De Rosa G, Onesimo R, Verusio V, Marino MV, Lanza GA, Rigante D, Tartaglia M, Zampino G. Leoni C, et al. Among authors: delogu ab. Am J Med Genet A. 2022 Feb;188(2):431-445. doi: 10.1002/ajmg.a.62529. Epub 2021 Oct 13. Am J Med Genet A. 2022. PMID: 34643321 Review.

5

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. 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.

6

Insights into the Cardiac Phenotype in 9p Deletion Syndrome: A Multicenter Italian Experience and Literature Review.

Pugnaloni F, Onesimo R, Blandino R, Putotto C, Versacci P, Delogu AB, Leoni C, Trevisan V, Croci I, Calì F, Digilio MC, Zampino G, Marino B, Calcagni G. Pugnaloni F, et al. Among authors: delogu ab. Genes (Basel). 2023 Jan 5;14(1):146. doi: 10.3390/genes14010146. Genes (Basel). 2023. PMID: 36672887 Free PMC article. Review.

7

Pulmonary artery sling in a 22-month-old boy with 18q deletion syndrome: A rare but possible association.

Delogu AB, Mariani F, Graziani F, Onesimo R, Savino G, Leoni C, Zampino G. Delogu AB, et al. Echocardiography. 2022 May;39(5):741-744. doi: 10.1111/echo.15349. Epub 2022 Apr 17. Echocardiography. 2022. PMID: 35434845

8

RASopathies and sigmoid-shaped ventricular septum morphology: evidence of a previously unappreciated cardiac phenotype.

Delogu AB, Blandino R, Leoni C, Tartaglia M, Zampino G. Delogu AB, et al. Pediatr Res. 2023 Mar;93(4):752-754. doi: 10.1038/s41390-022-02184-8. Epub 2022 Jul 6. Pediatr Res. 2023. PMID: 35794250 No abstract available.

9

Two case reports of fetal alcohol syndrome: broadening into the spectrum of cardiac disease to personalize and to improve clinical assessment.

Onesimo R, De Rose C, Delogu AB, Battista A, Leoni C, Veltri S, De Rosa G, Zampino G. Onesimo R, et al. Among authors: delogu ab. Ital J Pediatr. 2019 Dec 19;45(1):167. doi: 10.1186/s13052-019-0759-y. Ital J Pediatr. 2019. PMID: 31856879 Free PMC article.

10

A possible still role for colchicine in children with idiopathic recurrent acute pericarditis?

Tarantino G, Delogu AB, De Rosa G, Rigante D. Tarantino G, et al. Among authors: delogu ab. Intern Emerg Med. 2019 Mar;14(2):331-332. doi: 10.1007/s11739-018-1997-5. Epub 2018 Dec 5. Intern Emerg Med. 2019. PMID: 30519917 No abstract available.

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