Detalhe da pesquisa
1.
The 8th International RASopathies Symposium: Expanding research and care practice through global collaboration and advocacy.
Am J Med Genet A
; 194(4): e63477, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37969032
2.
Bioactive adrenomedullin (bio-ADM) is associated with endothelial dysfunction in infants and children with complex congenital heart disease undergoing open-heart surgery on cardiopulmonary bypass.
Clin Chem Lab Med
; 62(3): 551-561, 2024 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37870269
3.
Differentiating primary sarcomeric hypertrophic cardiomyopathy from Noonan syndrome: can the electrocardiogram be of use?
Cardiol Young
; 34(3): 597-603, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37649442
4.
EGFR and MMP-9 are associated with neointimal hyperplasia in systemic-to-pulmonary shunts in children with complex cyanotic heart disease.
Mamm Genome
; 34(2): 285-297, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36867212
5.
Genetic and phenotypic spectrum in the NONO-associated syndromic disorder.
Am J Med Genet A
; 191(2): 469-478, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36426740
6.
New prospectives on treatment opportunities in RASopathies.
Am J Med Genet C Semin Med Genet
; 190(4): 541-560, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36533679
7.
Low-molecular-weight heparin administered by subcutaneous catheter is a safe and effective anti-coagulation regimen in selected inpatient infants and children with complex congenital heart disease.
Cardiol Young
; 31(9): 1439-1444, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33588972
8.
Reasons for Failure of Systemic-to-Pulmonary Artery Shunts in Neonates.
Thorac Cardiovasc Surg
; 67(1): 2-7, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29351695
9.
Risk Factors for Failure of Systemic-to-Pulmonary Artery Shunts in Biventricular Circulation.
Pediatr Cardiol
; 39(7): 1323-1329, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29756161
10.
Clinical interpretation of KCNH2 variants using a robust PS3/BS3 functional patch-clamp assay.
HGG Adv
; 5(2): 100270, 2024 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38219013
11.
Mid-term results following pulmonary artery patch augmentation in congenital heart disease.
Transl Pediatr
; 12(11): 1992-2000, 2023 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38130592
12.
Epicardioid single-cell genomics uncovers principles of human epicardium biology in heart development and disease.
Nat Biotechnol
; 41(12): 1787-1800, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37012447
13.
Sudden cardiac death in childhood RASopathy-associated hypertrophic cardiomyopathy: Validation of the HCM risk-kids model and predictors of events.
Int J Cardiol
; 393: 131405, 2023 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37777071
14.
Cardiovascular Function and Exercise Capacity in Childhood Cancer Survivors.
J Clin Med
; 11(3)2022 Jan 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-35160079
15.
It Is Not Carved in Stone-The Need for a Genetic Reevaluation of Variants in Pediatric Cardiomyopathies.
J Cardiovasc Dev Dis
; 9(2)2022 Jan 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35200695
16.
Peak Oxygen Uptake on Cardiopulmonary Exercise Test Is a Predictor for Severe Arrhythmic Events during Three-Year Follow-Up in Patients with Complex Congenital Heart Disease.
J Cardiovasc Dev Dis
; 9(7)2022 Jul 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35877577
17.
Fetal Bradycardia Caused by Monogenic Disorders-A Review of the Literature.
J Clin Med
; 11(23)2022 Nov 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36498454
18.
Neointimal hyperplasia in systemic-to-pulmonary shunts of children with complex cyanotic congenital heart disease.
Eur J Cardiothorac Surg
; 62(6)2022 11 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36005853
19.
Management of cardiac aspects in children with Noonan syndrome - results from a European clinical practice survey among paediatric cardiologists.
Eur J Med Genet
; 65(1): 104372, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34757052
20.
European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe.
Eur J Med Genet
; 65(1): 104371, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34757053