Detalhe da pesquisa
1.
Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency.
Genet Med
; 24(3): 631-644, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34906488
2.
Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice.
PLoS Genet
; 13(1): e1006470, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28081210
3.
Prevalence and Progression of Late Gadolinium Enhancement in Children and Adolescents With Hypertrophic Cardiomyopathy.
Circulation
; 138(8): 782-792, 2018 08 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29622585
4.
Arrhythmias and fasciculoventricular pathways in patients with Danon disease: A single center experience.
J Cardiovasc Electrophysiol
; 30(10): 1932-1938, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31240821
5.
Endocardial Coronary Artery: A Rare Congenital Coronary Anomaly.
Pediatr Cardiol
; 40(1): 219-220, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30267109
6.
Anomalous Origin of Right Coronary Artery from the Non-coronary Cusp Demonstrated by Echocardiography and CT Angiography.
Pediatr Cardiol
; 40(2): 454-455, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30673798
7.
Incidental finding of type A aortic dissection in a paediatric heart transplant recipient.
Cardiol Young
; 29(9): 1219-1221, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31451126
8.
Prevalence of thoracic aortopathy in patients with juvenile Polyposis Syndrome-Hereditary Hemorrhagic Telangiectasia due to SMAD4.
Am J Med Genet A
; 167A(8): 1758-62, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25931195
9.
Sudden Cardiac Death: A Pediatrician's Role.
Pediatr Rev
; 40(9): 456-467, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31477588
10.
Transcatheter Aortic Valve Replacement in Congenital Heart Disease.
JACC Case Rep
; 29(4): 102199, 2024 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38379657
11.
Electrocardiographic QTc as a Surrogate Measure of Cardiac Risk in Children, Adolescents, and Young Adults With Eating Disorders.
Clin Pediatr (Phila)
; 62(6): 576-583, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36451274
12.
Multifocal disease progression and subsequent intervention in patients with actin alpha-2 variants: A single-center experience.
J Thorac Cardiovasc Surg
; 2023 Dec 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38065521
13.
Cardiac Remodeling in Subclinical Hypertrophic Cardiomyopathy: The VANISH Randomized Clinical Trial.
JAMA Cardiol
; 8(11): 1083-1088, 2023 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37672268
14.
Oxygen pulse kinetics in Fontan patients during treadmill ramp protocol cardiopulmonary exercise testing.
Pediatr Cardiol
; 33(8): 1301-6, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22466709
15.
Optimizing evaluation in pediatric and young adult patients with Marfan syndrome: Novel longitudinal metrics to track growth of aortic structures.
J Thorac Cardiovasc Surg
; 164(3): 724-740.e6, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35450696
16.
Correspondence to Vorselaars et al. thoracic aorta dilation in patients with hereditary hemorrhagic telangiectasia due to SMAD4 gene mutation.
Am J Med Genet A
; 170(3): 813, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26573265
17.
Management of the ventricular septal defect during double switch operation for atrioventricular discordant connections.
Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu
; 14(1): 29-34, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21444046
18.
Neonatal Ebstein anomaly national outcomes from 2000 to 2018 using the National Inpatient Sample.
Birth Defects Res
; 113(14): 1037-1043, 2021 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33788426
19.
Left Atrial Strain and Function in Pediatric Hypertrophic Cardiomyopathy.
J Am Soc Echocardiogr
; 34(9): 996-1006, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33915246
20.
Characteristics and Longer-Term Outcomes of Contemporary Patients <18 Years of Age With Hypertrophic Cardiomyopathy.
Am J Cardiol
; 140: 110-117, 2021 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33159906