Delogu A - Search Results

1

Diversity, parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome.

Zampino G, Pantaleoni F, Carta C, Cobellis G, Vasta I, Neri C, Pogna EA, De Feo E, Delogu A, Sarkozy A, Atzeri F, Selicorni A, Rauen KA, Cytrynbaum CS, Weksberg R, Dallapiccola B, Ballabio A, Gelb BD, Neri G, Tartaglia M. Zampino G, et al. Among authors: delogu a. Hum Mutat. 2007 Mar;28(3):265-72. doi: 10.1002/humu.20431. Hum Mutat. 2007. PMID: 17054105

2

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.

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. 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. 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

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. 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

6

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

7

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.

8

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.

9

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. Genes (Basel). 2023 Jan 5;14(1):146. doi: 10.3390/genes14010146. Genes (Basel). 2023. PMID: 36672887 Free PMC article. Review.

10

Admissions for acute cardiac inflammatory events or chest pain before and after the severe acute respiratory syndrome coronavirus 2 was in circulation.

Sodero G, Mariani F, Proli F, Lazzareschi I, Bersani G, Delogu AB, De Rosa G, Zampino G, Valentini P, Buonsenso D. Sodero G, et al. Acta Paediatr. 2023 May;112(5):1038-1040. doi: 10.1111/apa.16712. Epub 2023 Feb 25. Acta Paediatr. 2023. PMID: 36795000 No abstract available.

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