de Zorzi A - Search Results

1

Syndromic and Non-Syndromic Patients with Repaired Tetralogy of Fallot: Does It Affect the Long-Term Outcome?

Calcagni G, Calvieri C, Baban A, Bianco F, Barracano R, Caputo M, Madrigali A, Silva Kikina S, Perrone MA, Digilio MC, Pozzi M, Secinaro A, Sarubbi B, Galletti L, Gagliardi MG, de Zorzi A, Drago F, Leonardi B. Calcagni G, et al. Among authors: de zorzi a. J Clin Med. 2022 Feb 6;11(3):850. doi: 10.3390/jcm11030850. J Clin Med. 2022. PMID: 35160301 Free PMC article.

2

Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2.

Digilio MC, Marino B, Capolino R, Angioni A, Sarkozy A, Roberti MC, Conti E, de Zorzi A, Dallapiccola B. Digilio MC, et al. Among authors: de zorzi a. Am J Med Genet A. 2005 Apr 15;134A(2):158-64. doi: 10.1002/ajmg.a.30587. Am J Med Genet A. 2005. PMID: 15669097

3

LEOPARD syndrome: clinical diagnosis in the first year of life.

Digilio MC, Sarkozy A, de Zorzi A, Pacileo G, Limongelli G, Mingarelli R, Calabrò R, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: de zorzi a. Am J Med Genet A. 2006 Apr 1;140(7):740-6. doi: 10.1002/ajmg.a.31156. Am J Med Genet A. 2006. PMID: 16523510

4

Genetic heterogeneity and phenotypic anomalies in children with atrioventricular canal defect and tetralogy of Fallot.

Vergara P, Digilio MC, De Zorzi A, Di Carlo D, Capolino R, Rimini A, Pelegrini M, Calabro R, Marino B. Vergara P, et al. Among authors: de zorzi a. Clin Dysmorphol. 2006 Apr;15(2):65-70. doi: 10.1097/01.mcd.0000198925.94082.ea. Clin Dysmorphol. 2006. PMID: 16531730

5

Prevalence and clinical significance of cardiovascular abnormalities in patients with the LEOPARD syndrome.

Limongelli G, Pacileo G, Marino B, Digilio MC, Sarkozy A, Elliott P, Versacci P, Calabro P, De Zorzi A, Di Salvo G, Syrris P, Patton M, McKenna WJ, Dallapiccola B, Calabro R. Limongelli G, et al. Among authors: de zorzi a. Am J Cardiol. 2007 Aug 15;100(4):736-41. doi: 10.1016/j.amjcard.2007.03.093. Epub 2007 Jun 27. Am J Cardiol. 2007. PMID: 17697839

6

Costello syndrome: clinical diagnosis in the first year of life.

Digilio MC, Sarkozy A, Capolino R, Chiarini Testa MB, Esposito G, de Zorzi A, Cutrera R, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: de zorzi a. Eur J Pediatr. 2008 Jun;167(6):621-8. doi: 10.1007/s00431-007-0558-0. Epub 2007 Aug 29. Eur J Pediatr. 2008. PMID: 17726614

7

Congenital heart defects in patients with oculo-auriculo-vertebral spectrum (Goldenhar syndrome).

Digilio MC, Calzolari F, Capolino R, Toscano A, Sarkozy A, de Zorzi A, Dallapiccola B, Marino B. Digilio MC, et al. Among authors: de zorzi a. Am J Med Genet A. 2008 Jul 15;146A(14):1815-9. doi: 10.1002/ajmg.a.32407. Am J Med Genet A. 2008. PMID: 18553555

8

Aberrant left innominate artery from the left descending aorta in right aortic arch: echocardiographic diagnosis.

Barcudi S, Sanders SP, Di Donato RM, de Zorzi A, Iacobelli R, Amodeo A, Gagliardi MG, Borgia F, Pongiglione G, Rinelli G. Barcudi S, et al. Among authors: de zorzi a. J Am Soc Echocardiogr. 2010 Feb;23(2):221.e5-7. doi: 10.1016/j.echo.2009.08.013. Epub 2009 Oct 7. J Am Soc Echocardiogr. 2010. PMID: 19815384

9

Ultrasound tissue characterization of the myocardium in patients after Kawasaki disease.

Leonardi B, Giglio V, Sanders SP, Pasceri V, De Zorzi A. Leonardi B, et al. Among authors: de zorzi a. Pediatr Cardiol. 2010 Aug;31(6):766-72. doi: 10.1007/s00246-010-9694-9. Pediatr Cardiol. 2010. PMID: 20390262

10

Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart disease.

Guida V, Lepri F, Vijzelaar R, De Zorzi A, Versacci P, Digilio MC, Marino B, De Luca A, Dallapiccola B. Guida V, et al. Among authors: de luca a, de zorzi a. Dis Markers. 2010;28(5):287-92. doi: 10.3233/DMA-2010-0703. Dis Markers. 2010. PMID: 20592452 Free PMC article.

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