Detalhe da pesquisa
1.
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.
Am J Med Genet A
; 188(8): 2351-2359, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35491976
2.
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.
Am J Med Genet A
; 176(10): 2087-2098, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29663641
3.
Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease.
Eur J Med Genet
; 66(1): 104651, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36404488
4.
Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study.
Genes (Basel)
; 13(12)2022 12 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36553601
5.
Focus on Cardiologic Findings in 30 Children With PANS/PANDAS: An Italian Single-Center Observational Study.
Front Pediatr
; 7: 395, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31632938
6.
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice.
PLoS One
; 14(4): e0211170, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30933971
7.
Paroxysmal reciprocating supraventricular tachycardia in infants: electrophysiologically guided medical treatment and long-term evolution of the re-entry circuit.
Europace
; 10(5): 629-35, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18385122
8.
Conotruncal heart defects: impact of genetic syndromes on immediate operative mortality.
Ital Heart J
; 5(8): 624-8, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15554034
9.
[Transposition of great arteries. Understanding its pathogenesis]. / Trasposizione delle grandi arterie. Qualche spiraglio nell'inquadramento patogenetico.
Ital Heart J Suppl
; 3(2): 154-60, 2002 Feb.
Artigo
em Italiano
| MEDLINE | ID: mdl-11926021
10.
Genetic syndromes and outcome after surgical correction of tetralogy of Fallot.
Ann Thorac Surg
; 81(3): 968-75, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16488703
11.
Ventricular septal defect and deletion of chromosome 22q11: anatomical types and aortic arch anomalies.
Eur J Pediatr
; 161(2): 116-7, 2002 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-11954747