Detalhe da pesquisa
1.
Effect of deletion of the protein kinase PRKD1 on development of the mouse embryonic heart.
J Anat
; 2024 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38419169
2.
Medical education and training within congenital cardiology: current global status and future directions in a post COVID-19 world.
Cardiol Young
; 32(2): 185-197, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33843546
3.
Paediatric and adult congenital cardiology education and training in Europe.
Cardiol Young
; 32(12): 1966-1983, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-35227341
4.
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms.
Genet Med
; 23(1): 103-110, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32820247
5.
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.
Circ Res
; 124(4): 553-563, 2019 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30582441
6.
A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.
Hum Mol Genet
; 25(11): 2331-2341, 2016 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26965164
7.
Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects.
J Mol Cell Cardiol
; 106: 1-13, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28359939
8.
Rare variants in NR2F2 cause congenital heart defects in humans.
Am J Hum Genet
; 94(4): 574-85, 2014 04 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24702954
9.
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms.
Genet Med
; 24(4): 965, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-35394427
10.
Fifteen-minute consultation on limiting investigations in the fainting child.
Arch Dis Child Educ Pract Ed
; 101(1): 26-30, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26201347
11.
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.
Hum Mol Genet
; 22(7): 1473-81, 2013 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23297363
12.
Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
Am J Hum Genet
; 91(3): 489-501, 2012 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-22939634
13.
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.
Hum Mol Genet
; 21(7): 1513-20, 2012 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22199024
14.
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.
Am J Hum Genet
; 98(3): 592, 2016 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28863274
15.
Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times.
Eur J Pediatr
; 173(6): 757-65, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24384789
16.
Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot.
BMC Genet
; 14: 57, 2013 Jun 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-23782575
17.
Apixaban for Prevention of Thromboembolism in Pediatric Heart Disease.
J Am Coll Cardiol
; 82(24): 2296-2309, 2023 12 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38057072
18.
COVID-19 in congenital heart disease (COaCHeD) study.
Open Heart
; 10(2)2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37460271
19.
Alpha-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects.
Hum Mol Genet
; 19(20): 4007-16, 2010 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20656787
20.
Paediatric brain MRI findings following congenital heart surgery: a systematic review.
Arch Dis Child
; 107(9): 818-825, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35318194