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Reported practice patterns in the ambulatory care setting for patients with CHD.
- Published in:
- Cardiology in the Young, 2022, v. 32, n. 9, p. 1421, doi. 10.1017/S1047951121004303
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- Publication type:
- Article
Marked skeletal muscle deficits are associated with 6-minute walk distance in paediatric pulmonary hypertension.
- Published in:
- Cardiology in the Young, 2021, v. 31, n. 9, p. 1426, doi. 10.1017/S1047951121000342
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- Publication type:
- Article
Early postoperative remodelling following repair of tetralogy of Fallot utilising unsedated cardiac magnetic resonance: a pilot study.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Adult CHD: the ongoing need for physician counselling about heredity and contraceptive options.
- Published in:
- 2017
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- Publication type:
- journal article
Procollagen type III amino-terminal propeptide: a serum biomarker of left ventricular remodelling in paediatric dilated cardiomyopathy.
- Published in:
- Cardiology in the Young, 2015, v. 25, n. 2, p. 228, doi. 10.1017/S1047951113001820
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- Publication type:
- Article
22q11.2 deletion syndrome as a risk factor for aortic root dilation in tetralogy of Fallot.
- Published in:
- 2014
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- Publication type:
- journal article
The Congenital Heart Disease Genetic Network Study: Cohort description.
- Published in:
- PLoS ONE, 2018, v. 13, n. 1, p. 1, doi. 10.1371/journal.pone.0191319
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- Publication type:
- Article
Parental Impressions and Perspectives of Efficacy in Prenatal Counseling for Single Ventricle Congenital Heart Disease.
- Published in:
- Pediatric Cardiology, 2024, v. 45, n. 3, p. 605, doi. 10.1007/s00246-023-03355-y
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- Publication type:
- Article
Biomarkers, Socioeconomic Factors, and Right Ventricular Function After Surgical Repair for Tetralogy of Fallot.
- Published in:
- Pediatric Cardiology, 2023, v. 44, n. 6, p. 1232, doi. 10.1007/s00246-023-03108-x
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- Publication type:
- Article
Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome Without Intracardiac Anomalies.
- Published in:
- Pediatric Cardiology, 2021, v. 42, n. 7, p. 1594, doi. 10.1007/s00246-021-02645-7
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- Publication type:
- Article
Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 1, p. 265, doi. 10.1093/hmg/ddu420
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- Publication type:
- Article
Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 4, p. 648, doi. 10.1093/hmg/ddp532
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- Publication type:
- Article
Loss of RNA expression and allele-specific expression associated with congenital heart disease.
- Published in:
- Nature Communications, 2016, v. 7, n. 9, p. 12824, doi. 10.1038/ncomms12824
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- Publication type:
- Article
EM-mosaic detects mosaic point mutations that contribute to congenital heart disease.
- Published in:
- Genome Medicine, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13073-020-00738-1
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- Publication type:
- Article
Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation.
- Published in:
- Prenatal Diagnosis, 2024, v. 44, n. 6/7, p. 804, doi. 10.1002/pd.6566
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- Publication type:
- Article
Copy number variations in individuals with conotruncal heart defects reveal some shared developmental pathways irrespective of 22q11.2 deletion status.
- Published in:
- Birth Defects Research, 2019, v. 111, n. 13, p. 888, doi. 10.1002/bdr2.1534
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- Publication type:
- Article
Rare copy number variants in patients with congenital conotruncal heart defects.
- Published in:
- Birth Defects Research, 2017, v. 109, n. 4, p. 271, doi. 10.1002/bdra.23609
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- Publication type:
- Article
Longitudinal changes in adolescents with TOF: implications for care.
- Published in:
- European Heart Journal - Cardiovascular Imaging, 2017, v. 18, n. 3, p. 356, doi. 10.1093/ehjci/jew272
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- Publication type:
- Article
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study.
- Published in:
- Genes, 2023, v. 14, n. 1, p. 62, doi. 10.3390/genes14010062
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- Publication type:
- Article
Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States.
- Published in:
- Genes, 2021, v. 12, n. 7, p. 1030, doi. 10.3390/genes12071030
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- Publication type:
- Article
Common Variation in Cytoskeletal Genes Is Associated with Conotruncal Heart Defects.
- Published in:
- Genes, 2021, v. 12, n. 5, p. 655, doi. 10.3390/genes12050655
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- Publication type:
- Article
Determinants of Exercise Performance in Children and Adolescents with Repaired Tetralogy of Fallot Using Stress Echocardiography.
- Published in:
- Pediatric Cardiology, 2019, v. 40, n. 1, p. 71, doi. 10.1007/s00246-018-1962-0
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- Publication type:
- Article
Perioperative Factors Influence the Long-Term Outcomes of Children and Adolescents with Repaired Tetralogy of Fallot.
- Published in:
- Pediatric Cardiology, 2018, v. 39, n. 7, p. 1433, doi. 10.1007/s00246-018-1913-9
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- Publication type:
- Article
22q11.2 Deletion Status and Perioperative Outcomes for Tetralogy of Fallot with Pulmonary Atresia and Multiple Aortopulmonary Collateral Vessels.
- Published in:
- Pediatric Cardiology, 2018, v. 39, n. 5, p. 906, doi. 10.1007/s00246-018-1840-9
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- Publication type:
- Article
Quality of Life is Diminished in Patients with Tetralogy of Fallot with Mild Residual Disease: A Comparison of Tetralogy of Fallot and Isolated Valvar Pulmonary Stenosis.
- Published in:
- Pediatric Cardiology, 2017, v. 38, n. 8, p. 1645, doi. 10.1007/s00246-017-1709-3
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- Publication type:
- Article
Relationship Between Habitual Exercise and Performance on Cardiopulmonary Exercise Testing Differs Between Children With Single and Biventricular Circulations.
- Published in:
- Pediatric Cardiology, 2017, v. 38, n. 3, p. 472, doi. 10.1007/s00246-016-1537-x
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- Publication type:
- Article
The Impact of the Right Ventricular Outflow Tract Patch on Right Ventricular Strain in Tetralogy of Fallot: A Comparison with Valvar Pulmonary Stenosis Utilizing Cardiac Magnetic Resonance.
- Published in:
- Pediatric Cardiology, 2017, v. 38, n. 3, p. 617, doi. 10.1007/s00246-016-1558-5
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- Publication type:
- Article
Longitudinal Validation of the Diastolic to Systolic Time-Velocity Integral Ratio as a Doppler-Derived Measure of Pulmonary Regurgitation in Patients with Repaired Tetralogy of Fallot.
- Published in:
- Pediatric Cardiology, 2017, v. 38, n. 2, p. 240, doi. 10.1007/s00246-016-1505-5
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- Publication type:
- Article
The Impact of Pulmonary Insufficiency on the Right Ventricle: A Comparison of Isolated Valvar Pulmonary Stenosis and Tetralogy of Fallot.
- Published in:
- Pediatric Cardiology, 2015, v. 36, n. 4, p. 796, doi. 10.1007/s00246-014-1087-z
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- Publication type:
- Article
Morbidity in Children and Adolescents After Surgical Correction of Interrupted Aortic Arch.
- Published in:
- Pediatric Cardiology, 2014, v. 35, n. 3, p. 386, doi. 10.1007/s00246-013-0788-z
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- Publication type:
- Article
22q11.2 Deletions in Patients with Conotruncal Defects: Data from 1,610 Consecutive Cases.
- Published in:
- Pediatric Cardiology, 2013, v. 34, n. 7, p. 1687, doi. 10.1007/s00246-013-0694-4
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- Publication type:
- Article
Habitual Exercise Correlates With Exercise Performance in Patients With Conotruncal Abnormalities.
- Published in:
- Pediatric Cardiology, 2013, v. 34, n. 4, p. 853, doi. 10.1007/s00246-012-0556-5
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- Publication type:
- Article
Right Ventricular Strain Is Associated With Increased Length of Stay After Tetralogy of Fallot Repair.
- Published in:
- Journal of Cardiovascular Imaging, 2022, v. 30, n. 1, p. 50, doi. 10.4250/jcvi.2021.0069
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- Publication type:
- Article
22q11.2 deletion syndrome and congenital heart disease.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2020, v. 184, n. 1, p. 64, doi. 10.1002/ajmg.c.31774
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- Publication type:
- Article
Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 2, p. 137, doi. 10.1002/ajmg.b.32215
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- Publication type:
- Article
Association of genetic and sulcal traits with executive function in congenital heart disease.
- Published in:
- Annals of Clinical & Translational Neurology, 2024, v. 11, n. 2, p. 278, doi. 10.1002/acn3.51950
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- Publication type:
- Article
Genome-Wide Association Study of Maternal and Inherited Loci for Conotruncal Heart Defects.
- Published in:
- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0096057
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- Publication type:
- Article
Late effects in survivors of high‐risk neuroblastoma following stem cell transplant with and without total body irradiation.
- Published in:
- Pediatric Blood & Cancer, 2022, v. 69, n. 3, p. 1, doi. 10.1002/pbc.29537
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- Publication type:
- Article
Robust identification of mosaic variants in congenital heart disease.
- Published in:
- Human Genetics, 2018, v. 137, n. 2, p. 183, doi. 10.1007/s00439-018-1871-6
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- Publication type:
- Article
Diastolic dysfunction in tetralogy of Fallot: Comparison of echocardiography with catheterization.
- Published in:
- Echocardiography, 2018, v. 35, n. 10, p. 1641, doi. 10.1111/echo.14113
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- Publication type:
- Article
Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study.
- Published in:
- Journal of Cardiovascular Magnetic Resonance (BioMed Central), 2019, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12968-019-0555-2
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- Publication type:
- Article
Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects.
- Published in:
- PLoS ONE, 2020, v. 15, n. 6, p. 1, doi. 10.1371/journal.pone.0234357
- By:
- Publication type:
- Article
Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-74650-4
- By:
- Publication type:
- Article
CANOES: detecting rare copy number variants from whole exome sequencing data.
- Published in:
- Nucleic Acids Research, 2014, v. 42, n. 12, p. e97, doi. 10.1093/nar/gku345
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- Publication type:
- Article
Evaluating the role of connexin43 in congenital heart disease: Screening for mutations in patients with outflow tract anomalies and the analysis of knock-in mouse models.
- Published in:
- Journal of Cardiovascular Disease Research (Journal of Cardiovascular Disease Research), 2011, v. 2, n. 4, p. 206, doi. 10.4103/0975-3583.89804
- By:
- Publication type:
- Article
Late effects in survivors of tandem peripheral blood stem cell transplant for high-risk neuroblastoma.
- Published in:
- Pediatric Blood & Cancer, 2008, v. 51, n. 5, p. 679, doi. 10.1002/pbc.21683
- By:
- Publication type:
- Article
Mutational analysis of the PITX2 coding region revealed no common cause for transposition of the great arteries (dTGA).
- Published in:
- BMC Medical Genetics, 2005, v. 6, p. 1, doi. 10.1186/1471-2350-6-20
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- Publication type:
- Article
Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles.
- Published in:
- PLoS Genetics, 2020, v. 16, n. 11, p. 1, doi. 10.1371/journal.pgen.1009189
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- Publication type:
- Article
Gene-Gene Interactions in the Folate Metabolic Pathway and the Risk of Conotruncal Heart Defects.
- Published in:
- Journal of Biomedicine & Biotechnology, 2010, p. 1, doi. 10.1155/2010/630940
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- Publication type:
- Article