meta-analysis | Q815382 |
systematic review | Q1504425 |
scholarly article | Q13442814 |
P50 | author | Johanna Takkenberg | Q40276710 |
P2093 | author name string | Maarten Witsenburg | |
Denise van der Linde | |||
Jolien W. Roos-Hesselink | |||
Willem A. Helbing | |||
Elisabeth E.M. Konings | |||
Maarten A. Slager | |||
P433 | issue | 21 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | meta-analysis | Q815382 |
congenital heart disease | Q939364 | ||
congenital disorder | Q727096 | ||
systematic review | Q1504425 | ||
P304 | page(s) | 2241-7 | |
P577 | publication date | 2011-11-15 | |
P1433 | published in | Journal of the American College of Cardiology | Q2984355 |
P1476 | title | Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis | |
P478 | volume | 58 |
Q28087002 | 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of [...] |
Q89496905 | 320-slice Computed Tomography Angiography Imaging Findings and Follow-up in A Patient with Aortic Coarctation Misdiagnosed as Hypertension: A Case Report and Literature Review |
Q53318548 | 6q25.1 (TAB2) microdeletion syndrome: Congenital heart defects and cardiomyopathy. |
Q47630708 | A Big Five Personality Typology in Adolescents with Congenital Heart Disease: Prospective Associations with Psychosocial Functioning and Perceived Health |
Q33797800 | A Combined Independent Source Separation and Quality Index Optimization Method for Fetal ECG Extraction from Abdominal Maternal Leads. |
Q49559595 | A Functional Aryl Hydrocarbon Receptor Genetic Variant, Alone and in Combination with Parental Exposure, is a Risk Factor for Congenital Heart Disease |
Q50986749 | A Genetic Variant in FIGN Gene Reduces the Risk of Congenital Heart Disease in Han Chinese Populations. |
Q33702644 | A Gro/TLE-NuRD corepressor complex facilitates Tbx20-dependent transcriptional repression |
Q33683998 | A HAND to TBX5 Explains the Link Between Thalidomide and Cardiac Diseases. |
Q61444323 | A Matched Case-Control Study on the Association Between Colds, Depressive Symptoms during Pregnancy and Congenital Heart Disease in Northwestern China |
Q36071021 | A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease |
Q39194105 | A closer look at the developmental interplay between parenting and perceived health in adolescents with congenital heart disease |
Q90390572 | A de novo splicing variant supports the candidacy of TLL1 in ASD pathogenesis |
Q36596731 | A functional variant in the cystathionine β-synthase gene promoter significantly reduces congenital heart disease susceptibility in a Han Chinese population. |
Q35038105 | A genetic association study detects haplotypes associated with obstructive heart defects |
Q89790560 | A geometrically adaptable heart valve replacement |
Q95260935 | A glimpse of hope: cardiac surgery in low- and middle-income countries (LMICs) |
Q38774437 | A global view of pulmonary hypertension. |
Q41549089 | A missense mutation in TCN2 is associated with decreased risk for congenital heart defects and may increase cellular uptake of vitamin B12 via Megalin |
Q52479402 | A novel method for evaluating regional RV function in the adult congenital heart with low-dose CT and SQUEEZ processing. |
Q87687015 | A parent-of-origin analysis of paternal genetic variants and increased risk of conotruncal heart defects |
Q36135123 | A systematic review of prenatal screening for congenital heart disease by fetal electrocardiography |
Q36347014 | A telemedicine network for remote paediatric cardiology services in north-east Brazil |
Q47913935 | Additive effect of congenital heart disease and early developmental disorders on attention-deficit/hyperactivity disorder and autism spectrum disorder: a nationwide population-based longitudinal study |
Q64076221 | Adults With Complex Congenital Heart Disease: Cerebrovascular Considerations for the Neurologist |
Q58121826 | Advanced Imaging to Phenotype Patients With a Systemic Right Ventricle |
Q38761378 | Advanced flow MRI: emerging techniques and applications. |
Q38301475 | Advances in the Care of Adults With Congenital Heart Disease |
Q52663753 | Advances in the Understanding of the Genetic Determinants of Congenital Heart Disease and Their Impact on Clinical Outcomes. |
Q48191843 | Advancing Prenatal Detection of Congenital Heart Disease: A Novel Screening Protocol Improves Early Diagnosis of Complex Congenital Heart Disease |
Q30245358 | Adverse outcome of coarctation stenting in patients with Turner syndrome |
Q94038750 | Akap12beta supports asymmetric heart development via modulating the Kupffer’s vesicle formation in zebrafish |
Q38968650 | Alkaline Phosphatase: A Biomarker of Cardiac Function in Pediatric Patients |
Q91519463 | Altered in utero kidney development in newborns with congenital heart disease |
Q60446914 | Ambient air pollution and congenital heart defects in Lanzhou, China |
Q40805578 | An empowerment health education program for children undergoing surgery for congenital heart diseases |
Q64114068 | An integrated in utero MR method for assessing structural brain abnormalities and measuring intracranial volumes in fetuses with congenital heart disease: results of a prospective case-control feasibility study |
Q88323907 | An international survey of management of pain and sedation after paediatric cardiac surgery |
Q52429196 | An interspecies heart-to-heart: Using Xenopus to uncover the genetic basis of congenital heart disease. |
Q42362384 | Analyses of trends in prevalence of congenital heart defects and folic acid supplementation |
Q37336399 | Analysis of Surgical Mortality for Congenital Heart Defects Using RACHS-1 Risk Score in a Brazilian Single Center |
Q89822660 | Analysis of congenital heart surgery results: A comparison of four risk scoring systems |
Q47569932 | Analysis of the psychosocial impact of caretaking on the parents of an infant with severe congenital heart defect |
Q57300723 | Anatomy of the atrial septum and interatrial communications |
Q55029222 | Anesthetic Implications for Cesarean Section in a Parturient with Complex Congenital Cyanotic Heart Disease. |
Q94596717 | Anesthetic Management for Heart Transplantation in Adults with Congenital Heart Disease |
Q37229564 | Anesthetic Management of Urgent Cesarean Section with Undiagnosed Transposition of Great Arteries |
Q38799170 | Applications of 3D printing in cardiovascular diseases |
Q36090080 | Are hypertensive disorders in pregnancy associated with congenital malformations in offspring? Evidence from the WHO Multicountry cross sectional survey on maternal and newborn health |
Q53112372 | Ascending aortic diameters in congenital aortic stenosis: cardiac magnetic resonance versus transthoracic echocardiography. |
Q49395162 | Assessment of PIM-2 performance among surgical patients with heart disease and correlation of results with RACHS-1. |
Q87095985 | Association Between Sequence Variations in RCAN1 Promoter and the Risk of Sporadic Congenital Heart Disease in a Chinese Population |
Q49191433 | Association Between Tetralogy of Fallot and Tracheobronchial Branching Abnormalities: A New Clue for Pathogenesis? |
Q85919780 | Association Between the 4p16 Susceptibility Locus and the Risk of Atrial Septal Defect in Population from Southeast China |
Q40632719 | Association analysis identifies new risk loci for congenital heart disease in Chinese populations |
Q34380409 | Association between 5, 10-methylenetetrahydrofolate reductase (MTHFR) polymorphisms and congenital heart disease: A meta-analysis |
Q28397471 | Association between maternal exposure to housing renovation and offspring with congenital heart disease: a multi-hospital case-control study |
Q98204218 | Association between prepregnancy body mass index and risk of congenital heart defects in offspring: an ambispective observational study in China |
Q37043170 | Association between pulmonary hypertension and an atrial septal defect |
Q57166977 | Association of Atrial Septal Defects and Bronchopulmonary Dysplasia in Premature Infants |
Q86549914 | Association of DNMT1 Gene Polymorphisms with Congenital Heart Disease in Child Patients |
Q64068848 | Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children |
Q90266461 | Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios |
Q51020875 | Association of TGFBR2 rs6785358 Polymorphism with Increased Risk of Congenital Ventricular Septal Defect in a Chinese Population. |
Q34988392 | Association of two variants in SMAD7 with the risk of congenital heart disease in the Han Chinese population |
Q89855759 | Associations between fine particulate matter, extreme heat events, and congenital heart defects |
Q34926370 | Associations between two genetic variants in NKX2-5 and risk of congenital heart disease in Chinese population: a meta-analysis |
Q91610736 | Associations of maternal upper respiratory tract infection/influenza during early pregnancy with congenital heart disease in offspring: evidence from a case-control study and meta-analysis |
Q46170228 | Atrial ERK1/2 activation in the embryo leads to incomplete Septal closure: a novel mouse model of atrial Septal defect |
Q47294138 | Atrial Fibrillation in Patients with Congenital Heart Disease |
Q55280534 | Atrial Septal Defect as Unexpected Cause of Pulmonary Artery Hypertension. |
Q57300719 | Atrial septal defect and exercise capacity: value of cardio-pulmonary exercise test in assessment and follow-up |
Q53642805 | Atrial septal defect repair gone wrong. |
Q57300715 | Atrial septal defect with pulmonary hypertension: when/how can we consider closure? |
Q57300706 | Atrial septal defects and pulmonary arterial hypertension |
Q90435046 | Atrial septal defects, supravalvular aortic stenosis and syndromes predisposing to aneurysm of large vessels |
Q33854123 | Atrial tachyarrhythmia in adult congenital heart disease |
Q36984755 | Bayesian multinomial probit modeling of daily windows of susceptibility for maternal PM2.5 exposure and congenital heart defects |
Q38002054 | Benefits of predischarge echocardiography service for postnatal heart murmurs |
Q44267266 | Between invisible defects and visible impact: the life experiences of adolescents and young adults with congenital heart disease |
Q88101846 | Beyond Gene Panels: Whole Exome Sequencing for Diagnosis of Congenital Heart Disease |
Q38113254 | Biomarkers in congenital heart disease: do natriuretic peptides hold the key? |
Q98771445 | Birth Defects Data From Population-Based Birth Defects Surveillance System in a District of Southern Jiangsu, China, 2014-2018 |
Q31036974 | Birth defects data from surveillance hospitals in Dalian city, China, 2006-2010. |
Q40993972 | Birth prevalence of congenital heart disease: A cross-sectional observational study from North India |
Q36651978 | Bringing Antonovsky's salutogenic theory to life: A qualitative inquiry into the experiences of young people with congenital heart disease |
Q93200082 | CACCT: An Automated Tool of Detecting Complicated Cardiac Malformations in Mouse Models |
Q34500979 | CRISPR/Cas9: An inexpensive, efficient loss of function tool to screen human disease genes in Xenopus. |
Q57665132 | CSI position statement on management of heart failure in India |
Q42578498 | CT imaging features of atrioventricular shunts: what the radiologist must know |
Q89094804 | Calcitriol trend following pediatric cardiac surgery and association with clinical outcome |
Q59339785 | Can echocardiographic screening in the early days of life detect critical congenital heart disease among apparently healthy newborns? |
Q59137245 | Cardiac Catheterization in the Early Post-Operative Period after Congenital Heart Surgery |
Q49410654 | Cardiac Conduction System in Congenitally Corrected Transposition of the Great Arteries and Its Clinical Relevance |
Q47624132 | Cardiac Denial and Psychological Predictors of Cardiac Care Adherence in Adults With Congenital Heart Disease. |
Q92321358 | Cardiac catheterisation in infants weighing less than 2500 grams |
Q38304855 | Cardiac magnetic resonance imaging in children |
Q53067631 | Cardiac manifestations of Pallister-Killian syndrome. |
Q42784094 | Cardiac neural crest ablation results in early endocardial cushion and hemodynamic flow abnormalities. |
Q38135363 | Cardiac outflow tract anomalies |
Q37430060 | Cardiac surgery in Africa: a thirty-five year experience on open heart surgery in Cote d'Ivoire |
Q40067710 | Cardiac surgery in adults with high-surgical complexity CHD: results of a network collaborative programme. |
Q37234055 | CardioTF, a database of deconstructing transcriptional circuits in the heart system |
Q55234674 | Cardiopulmonary bypass reduces myocardial oxidative stress, inflammation and increases c-kit+CD45- cell population in newborns. |
Q96137391 | Cardiovascular Diseases in Sub-Saharan Africa Compared to High-Income Countries: An Epidemiological Perspective |
Q42366025 | Case Report: Emergency awake craniotomy for cerebral abscess in a patient with unrepaired cyanotic congenital heart disease. |
Q57074709 | Caval to pulmonary 3D flow distribution in patients with Fontan circulation and impact of potential 4D flow MRI error sources |
Q41101035 | Cerebral Microhemorrhage: A Frequent Magnetic Resonance Imaging Finding in Pediatric Patients after Cardiopulmonary Bypass |
Q38809638 | Changes in the diagnosis of congenital cardiovascular malformations during the 1st year of life: impacts on epidemiological risk factor associations |
Q59173723 | Changing patterns of patent ductus arteriosus surgical ligation in the United States |
Q87867168 | Changing prevalence of severe congenital heart disease: a population-based study |
Q34105420 | Characterization of circulating microRNA expression in patients with a ventricular septal defect |
Q47560574 | Children's experiences of congenital heart disease: a systematic review of qualitative studies |
Q33640889 | Chromosome microarray analysis in the investigation of children with congenital heart disease |
Q35228294 | Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield |
Q26744645 | Circulating microRNAs as potential biomarkers for diagnosis of congenital heart defects |
Q90467222 | Clinical and postmortem findings of pentalogy of Fallot in an 18-month-old Holstein heifer |
Q38941786 | Clinical predictors of length of stay in adults with congenital heart disease |
Q52684687 | Clinical significance of circulating microRNAs as markers in detecting and predicting congenital heart defects in children. |
Q37587382 | Coexistence of abnormal systolic motion of mitral valve in a consecutive group of 324 adult Tetralogy of Fallot patients assessed with echocardiography. |
Q91876306 | Comparative proteomic analysis of plasma of children with congenital heart disease |
Q38217759 | Computational modeling of Fontan physiology: at the crossroads of pediatric cardiology and biomedical engineering |
Q38512145 | Concise Review: Cardiac Disease Modeling Using Induced Pluripotent Stem Cells. |
Q93017983 | Congenital Heart Defects in Monochorionic Twins: A Systematic Review and Meta-Analysis |
Q40488157 | Congenital Heart Disease in Premature Infants 25-32 Weeks' Gestational Age. |
Q58691537 | Congenital heart defect repair with ADAPT tissue engineered pericardium scaffold: An early-stage health economic model |
Q102073873 | Congenital heart defects in patients with isolated microtia: evaluation using colour Doppler echocardiographic image |
Q52654307 | Congenital heart disease and aortic arch variants associated with mutation in PHOX2B. |
Q37267579 | Congenital heart disease and rheumatic heart disease in Africa: recent advances and current priorities |
Q38150590 | Congenital heart disease in 37,294 births in Tunisia: birth prevalence and mortality rate |
Q92917001 | Congenital heart disease: a global public health concern |
Q26859219 | Congenital heart disease: emerging themes linking genetics and development |
Q39092344 | Congenital heart disease: the crossroads of genetics, epigenetics and environment |
Q50673883 | Consanguinity and isolated atrial septal defect in North East of Iran. |
Q36619795 | Continuous and Pulsatile Pediatric Ventricular Assist Device Hemodynamics with a Viscoelastic Blood Model |
Q46564299 | Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands. |
Q47778515 | Coronary artery assessment using self-navigated free-breathing radial whole-heart magnetic resonance angiography in patients with congenital heart disease. |
Q33683825 | Correlation of electrocardiogram parameters and hemodynamic outcomes in patients with isolated secundum atrial septal defects |
Q90347635 | Counseling for Prenatal Congenital Heart Disease-Recommendations Based on Empirical Assessment of Counseling Success |
Q35536567 | Coverage of the 2011 Q fever vaccination campaign in the Netherlands, using retrospective population-based prevalence estimation of cardiovascular risk-conditions for chronic Q fever |
Q36033594 | Current advances in the translation of vascular tissue engineering to the treatment of pediatric congenital heart disease. |
Q90052771 | Current outcomes and treatment of tetralogy of Fallot |
Q36087912 | Cyanotic congenital heart disease the coronary arterial circulation |
Q41598696 | Cyanotic congenital heart diseases among Nigerian children |
Q64080456 | DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome |
Q93270302 | De novo damaging variants associated with congenital heart diseases contribute to the connectome |
Q39343128 | De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease. |
Q36245207 | Defining the Risk and Associated Morbidity and Mortality of Severe Respiratory Syncytial Virus Infection Among Infants with Congenital Heart Disease |
Q47790092 | Dental prevention and disease awareness in children with congenital heart disease |
Q34289011 | Depolarization of Cellular Resting Membrane Potential Promotes Neonatal Cardiomyocyte Proliferation In Vitro. |
Q33705120 | Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression |
Q45905502 | Determinants of physical activity in young adults with tetralogy of Fallot. |
Q38356229 | Determinants of quality of life in children and adolescents with CHD: a systematic review |
Q40672571 | Development and persistence of depressive symptoms in adolescents with CHD. |
Q50057648 | Development and preliminary testing of the Brief Developmental Assessment: an early recognition tool for children with heart disease. |
Q98895745 | Development of Tissue Engineered Heart Valves for Percutaneous Transcatheter Delivery in a Fetal Ovine Model |
Q33619577 | Development of an Online, Evidence-Based Patient Information Portal for Congenital Heart Disease: A Pilot Study |
Q92401219 | Development of feeding information for infants with CHD |
Q93016403 | Dextro-transposition of the great arteries: switching the switch |
Q39453072 | Differences by Altitude in the Frequency of Congenital Heart Defects in Colombia. |
Q55267355 | Differential Expression of CircRNAs in Embryonic Heart Tissue Associated with Ventricular Septal Defect. |
Q33742505 | Differential expression of microRNAs following cardiopulmonary bypass in children with congenital heart diseases |
Q64268697 | Differential localizations of protein phosphatase 1 isoforms determine their physiological function in the heart |
Q28509591 | Disruption of G-protein γ5 subtype causes embryonic lethality in mice |
Q43378616 | Dissecting the Role of the Extracellular Matrix in Heart Disease: Lessons from the Drosophila Genetic Model |
Q91659641 | Does Inhaled Milrinone Facilitate Weaning From Cardiopulmonary Bypass in Children with Congenital Heart Diseases Complicated with Pulmonary Arterial Hypertension? |
Q35936208 | Drug use in children hospitalized with cardio-rheumatologic diseases in Andijan, Uzbekistan: a cross-sectional descriptive study |
Q47963242 | Dysphagia in infants with single ventricle anatomy following stage 1 palliation: Physiologic correlates and response to treatment. |
Q37672488 | Early Complications After Percutaneous Closure of Atrial Septal Defect in Infants with Procedural Weight Less than 15 kg |
Q35724908 | Early fetal echocardiography: Experience of a tertiary diagnostic service |
Q88447885 | Early life environment and social determinants of cardiac health in children with congenital heart disease |
Q90171404 | Early postnatal cardiac follow-up of survivors of twin-twin transfusion syndrome treated with fetoscopic laser coagulation |
Q34483257 | Early pregnancy exposure to selective serotonin reuptake inhibitors, risks of major structural malformations, and hypothesized teratogenic mechanisms |
Q97527839 | Educational Case: Tetralogy of Fallot and a Review of the Most Common Forms of Congenital Heart Disease |
Q58127400 | Effect of Fetal Growth on 1-Year Mortality in Neonates With Critical Congenital Heart Disease |
Q91762327 | Effect of corrective or palliative procedures on arterial to end-tidal carbon dioxide pressure difference in pediatric cardiac surgery |
Q91249002 | Effect of family socioeconomic status on the prognosis of complex congenital heart disease in children: an observational cohort study from China |
Q89762996 | Effects of Exercise Training in Postoperative Patients With Congenital Heart Disease: A Systematic Review and Meta-Analysis of Randomized Controlled Trials |
Q52663514 | Efficacy and Safety of Low-Dose Amiodarone Therapy for Tachyarrhythmia in Congenital Heart Disease. |
Q38802463 | Efficacy of prenatal diagnosis of major congenital heart disease on perinatal management and perioperative mortality: a meta-analysis |
Q89458667 | Electrocardiographic RR and QT Interval Variability in Patients with Atrial Septal Defect and Healthy Children |
Q39919059 | Elevated birth prevalence of conotruncal heart defects in a population with high consanguinity rate. |
Q51308628 | Elevated serum levels of ghrelin and TNF-α in patients with cyanotic and acyanotic congenital heart disease. |
Q90752916 | Emerging trends in the prenatal diagnosis of complex CHD and its influence on infant mortality in this cohort |
Q47073088 | Endogenous Natural Complement Inhibitor Regulates Cardiac Development |
Q28277874 | Endothelial deletion of murine Jag1 leads to valve calcification and congenital heart defects associated with Alagille syndrome |
Q41686240 | Enlargement Ratio May Predict Device Size in Elderly Patients with Atrial Septal Defect. |
Q58802172 | Epidemiology and major subtypes of congenital heart defects in Hunan Province, China |
Q35904831 | Epidemiology of Birth Defects Based on a Birth Defect Surveillance System from 2005 to 2014 in Hunan Province, China |
Q85456012 | Epidemiology of congenital heart disease in Brazil |
Q98735533 | Essential Role of Complement in Pregnancy: From Implantation to Parturition and Beyond |
Q38635016 | Estimated Maternal Pesticide Exposure from Drinking Water and Heart Defects in Offspring |
Q92881212 | Estimating the effect size of the 15Q11.2 BP1-BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice |
Q58593929 | Ethics in humanitarian efforts: when should resources be allocated to paediatric heart surgery? |
Q33785529 | Ethnic and socioeconomic variation in incidence of congenital heart defects |
Q30203057 | Evaluating cost and resource use associated with pulse oximetry screening for critical congenital heart disease: Empiric estimates and sources of variation |
Q50560216 | Evaluation of Neurodevelopment Using Bayley-III in Children with Cyanotic or Hemodynamically Impaired Congenital Heart Disease. |
Q36217168 | Evaluation of regulatory genetic variants in POU5F1 and risk of congenital heart disease in Han Chinese |
Q98188972 | Evaluation of renal injury in children with uncorrected CHDs with significant shunt using urinary neutrophil gelatinase-associated lipocalin |
Q39484829 | Evaluation of swallowing in infants with congenital heart defect |
Q97886699 | Evolution of blood biomarker levels following percutaneous atrial septal defect closure in adults |
Q49367360 | Evolution of membrane oxygenator technology for utilization during pediatric cardiopulmonary bypass |
Q38346860 | Experiences and Outcomes of Transition from Pediatric to Adult Health Care Services for Young People with Congenital Heart Disease: A Systematic Review |
Q92732020 | Exploring the Prognostic Value of Novel Markers in Adults With a Systemic Right Ventricle |
Q55051861 | Exposure to Nitrogen Oxide in the First Trimester and Risk of Cardiovascular-Related Malformations: A Dose-Response Meta-Analysis of Observational Studies. |
Q37248612 | Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature |
Q47441811 | Fetal nuchal translucency in severe congenital heart defects: experiences in Northern Finland |
Q38075509 | Folate, homocysteine and the cardiac neural crest |
Q50216054 | Folate, vitamin B12, homocysteine and polymorphisms in folate metabolizing genes in children with congenital heart disease and their mothers |
Q55350895 | Frequency and Outcome of Acute Neurologic Complications after Congenital Heart Disease Surgery. |
Q36697854 | Frequency and pattern of congenital heart defects in a tertiary care cardiac hospital of Karachi |
Q40554492 | Frequent atrial extrasystolic beats predict atrial fibrillation in patients with congenital heart defects |
Q38493240 | From zebrafish heart jogging genes to mouse and human orthologs: using Gene Ontology to investigate mammalian heart development |
Q38430025 | Functional Analyses of a Novel CITED2 Nonsynonymous Mutation in Chinese Tibetan Patients with Congenital Heart Disease |
Q90075489 | Functional analysis of rare variants of GATA4 identified in Chinese patients with congenital heart defect |
Q92015525 | Functional analysis of the congenital heart disease‑associated GATA4 H436Y mutation in vitro |
Q51142741 | Functional and haemodynamic assessment of mild-to-moderate pulmonary valve stenosis at rest and during exercise. |
Q34629093 | Functional knowledge transfer for high-accuracy prediction of under-studied biological processes |
Q24321906 | GATA4 loss-of-function mutations underlie familial tetralogy of fallot |
Q36501505 | GATA5 loss-of-function mutations underlie tetralogy of fallot |
Q100548918 | GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm |
Q91844788 | GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum |
Q92240511 | Gata4 regulates hedgehog signaling and Gata6 expression for outflow tract development |
Q46441365 | Generation of Nkx2-5/CreER transgenic mice for inducible Cre expression in developing hearts. |
Q90669133 | Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association |
Q58749774 | Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects |
Q64057042 | Genetic polymorphisms in MTR are associated with non-syndromic congenital heart disease from a family-based case-control study in the Chinese population |
Q30235241 | Genetics and Genomics of Congenital Heart Disease |
Q26862793 | Genetics of congenital heart disease: the glass half empty |
Q96817087 | Genomic analyses implicate noncoding de novo variants in congenital heart disease |
Q63493302 | Genomics and Epigenomics of Congenital Heart Defects: Expert Review and Lessons Learned in Africa |
Q98184319 | Geographical variations in maternal lifestyles during pregnancy associated with congenital heart defects among live births in Shaanxi province, Northwestern China |
Q98611637 | Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms |
Q98161487 | Global Burden of Congenital Heart Disease: Experience in Korea as a Potential Solution to the Problem |
Q64230541 | Global birth prevalence of congenital heart defects 1970-2017: updated systematic review and meta-analysis of 260 studies |
Q92917023 | Global, regional, and national burden of congenital heart disease, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017 |
Q26862091 | HIF hydroxylase pathways in cardiovascular physiology and medicine |
Q37353579 | HIRA Gene is Lower Expressed in the Myocardium of Patients with Tetralogy of Fallot |
Q92800232 | Health-related quality of life (HRQOL) in children and adolescents with congenital heart disease: a cross-sectional survey from South India |
Q47095779 | Health-related quality of life in congenital heart disease surgery patients in Pakistan: protocol for a mixed-methods study |
Q53786442 | Healthcare needs of adolescents with congenital heart disease transitioning into adulthood: a Delphi survey of patients, parents, and healthcare providers. |
Q22306356 | Heart Disease and Stroke Statistics--2013 Update: A Report From the American Heart Association |
Q22241921 | Heart Disease and Stroke Statistics--2015 Update: A Report From the American Heart Association |
Q30238784 | Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association |
Q64102633 | Heart Rate Response During Treadmill Exercise Test in Children and Adolescents With Congenital Heart Disease |
Q29547691 | Heart disease and stroke statistics--2014 update: a report from the American Heart Association |
Q44030613 | Heart failure in adult congenital heart disease |
Q92983500 | Heart regeneration with human pluripotent stem cells: Prospects and challenges |
Q38041426 | Heavy and light roles: myosin in the morphogenesis of the heart |
Q48172018 | Hemodynamics Modify Collagen Deposition in the Early Embryonic Chicken Heart Outflow Tract. |
Q36283869 | Histone Deacetylase 3 Coordinates Deacetylase-independent Epigenetic Silencing of Transforming Growth Factor-β1 (TGF-β1) to Orchestrate Second Heart Field Development |
Q90527320 | Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variants |
Q64095264 | Home care experience and nursing needs of caregivers of children undergoing congenital heart disease operations: A qualitative descriptive study |
Q37580574 | Hot Days in Early Pregnancy: A Potential Risk Factor for Congenital Heart Defects |
Q90955670 | Hypophosphataemia in infants with CHD treated with amino acid infant formula |
Q91949720 | Identification and analysis of KLF13 variants in patients with congenital heart disease |
Q49376076 | Identification of Novel Congenital Heart Disease Candidate Genes Using Chromosome Microarray |
Q47668199 | Identification of ZFPM2 mutations in sporadic conotruncal heart defect patients |
Q57180807 | Identification of clinically actionable variants from genome sequencing of families with congenital heart disease |
Q47246530 | Identification of key genes associated with congenital heart defects in embryos of diabetic mice |
Q49270535 | Identification of novel genomic imbalances in Saudi patients with congenital heart disease. |
Q90013695 | Identification of rare variants in novel candidate genes in pulmonary atresia patients by next generation sequencing |
Q92756467 | Identification of risk factors affecting catch-up growth after infant congenital heart disease surgery: rationale and design of a multicentre prospective cohort study in China |
Q58193248 | Identification ofTBX5mutations in a series of 94 patients with Tetralogy of Fallot |
Q52691066 | Illness Identity in Adults with a Chronic Illness. |
Q55499300 | Illness Identity: A Novel Predictor for Healthcare Use in Adults With Congenital Heart Disease. |
Q47101646 | Immediate Therapeutic Outcomes and Medium-term Follow-up of Percutaneous Balloon Pulmonary Valvuloplasty in Infants with Pulmonary Valve Stenosis: A Single-center Retrospective Study |
Q61797789 | Impact of Congenital Cardiac Catheterization Project on Outcomes-Quality Improvement (C3PO-QI) in LMICs |
Q39702559 | Impact of Telemedicine in the Screening for Congenital Heart Disease in a Center from Northeast Brazil |
Q90682115 | Impact of congenital heart disease on siblings: A review |
Q45947454 | Impact of introduction of 20-week ultrasound scan on prevalence and fetal and neonatal outcomes in cases of selected severe congenital heart defects in The Netherlands. |
Q100385067 | Impact of pulmonary hypertension and congenital heart disease with hemodynamic repercussion on the severity of acute respiratory infections in children under 5 years of age at a pediatric referral center in Colombia, South America |
Q94600033 | Impact of standardized prenatal documentation among newborns with ductal-dependent heart disease |
Q41396365 | Improved passive catheter tracking with positive contrast for CMR-guided cardiac catheterization using partial saturation (pSAT). |
Q36969773 | Improving Outcomes for Infants with Single Ventricle Physiology through Standardized Feeding during the Interstage. |
Q38744367 | Improving the quality of transition and transfer of care in young adults with congenital heart disease. |
Q58695466 | In Utero Diagnoses of Strikingly Similar Presentations of Complete Atrioventricular Septal Defects in a Pair of Dizygotic Twins Concordant for Trisomy 21 |
Q91437048 | Incidence and Risk Factors of Cardiac Abnormalities in Patients with Idiopathic Scoliosis |
Q38600490 | Incidence and natural history of neonatal isolated ventricular septal defects: Do we know everything? A 6-year single-center Italian experience follow-up |
Q36074912 | Incidence of Congenital Heart Disease: The 9-Year Experience of the Guangdong Registry of Congenital Heart Disease, China |
Q87346202 | Incidences and sociodemographics of specific congenital heart diseases in the United States of America: an evaluation of hospital discharge diagnoses |
Q47927467 | Incidental Findings on Routine Targeted Neonatal Echocardiography Performed in Preterm Neonates Younger Than 29 Weeks' Gestation |
Q38955624 | Increased regurgitant flow causes endocardial cushion defects in an avian embryonic model of congenital heart disease. |
Q39156923 | Increasing mortality burden among adults with complex congenital heart disease. |
Q36138033 | Indigenous Ethnicity and Low Maternal Education Are Associated with Delayed Diagnosis and Mortality in Infants with Congenital Heart Defects in Panama |
Q96950772 | Induced pluripotent stem cells of patients with Tetralogy of Fallot reveal transcriptional alterations in cardiomyocyte differentiation |
Q38958010 | Infective endocarditis after device closure of atrial septal defects: Case report and review of the literature. |
Q34015565 | Inhibition of histone H3K9 acetylation by anacardic acid can correct the over-expression of Gata4 in the hearts of fetal mice exposed to alcohol during pregnancy |
Q37567142 | Inhibition of histone acetylation by curcumin reduces alcohol-induced fetal cardiac apoptosis |
Q100389189 | Innovative approach to identify multigenomic and environmental interactions associated with birth defects in family-based hybrid designs |
Q47243152 | Integrated rare variant-based risk gene prioritization in disease case-control sequencing studies. |
Q58617588 | Integrative regulation of physiology by histone deacetylase 3 |
Q24198254 | Interventions to increase physical activity for people with congenital heart disease |
Q58568609 | Intraatrial reentrant tachycardia originating from the prior suture line of the baffle in a patient who underwent the Mustard operation: Ultra-high-density 3-dimensional mapping |
Q50551887 | Intraoperative arrhythmias in children with congenital heart disease: transient, innocent events? |
Q55266754 | Intravenous morphine versus intravenous paracetamol after cardiac surgery in neonates and infants: a study protocol for a randomized controlled trial. |
Q99350021 | Investigating altered brain development in infants with congenital heart disease using tensor-based morphometry |
Q89870051 | Iron-deficiency anaemia in children with congenital heart diseases at a teaching hospital in Ghana |
Q38583690 | Is pre-discharge echocardiography indicated for asymptomatic neonates with a heart murmur? A retrospective analysis |
Q57316848 | Isolated ventricular septal defects in the era of advanced fetal echocardiography: risk of chromosomal anomalies and spontaneous closure rate from diagnosis to age of 1 year |
Q49555073 | JNK and NF-κB signaling pathways are involved in cytokine changes in patients with congenital heart disease prior to and after transcatheter closure |
Q37341781 | KinCor, a national registry for paediatric patients with congenital and other types of heart disease in the Netherlands: aims, design and interim results |
Q91352674 | Lack of access to paediatric cardiology services in the public health system in four major urban centres in Perú |
Q89141425 | Large bilateral adrenal haemorrhages in a newborn with unrepaired cyanotic CHD |
Q47099175 | Late Onset Postcapillary Pulmonary Hypertension in Patients With Transposition of the Great Arteries and Mustard or Senning Baffles |
Q38828534 | Late gadolinium enhancement and adverse outcomes in a contemporary cohort of adult survivors of tetralogy of Fallot |
Q50868084 | Levels of Circulating mRNA for the Tenascin-X (TNXB) Gene in Maternal Plasma at the Second Trimester in Pregnancies with Isolated Congenital Ventricular Septal Defects. |
Q47550901 | Long-term Associations of an Early Corrected Ventricular Septal Defect and Stress Systems of Child and Mother at Primary School Age. |
Q52859774 | Long-term healing of mildly cross-linked decellularized bovine pericardial aortic patch. |
Q45223105 | Long-term outcome and quality of life after arterial switch operation: a prospective study with a historical comparison |
Q40833536 | Longitudinal development of psychopathology and subjective health status in CHD adults: a 30- to 43-year follow-up in a unique cohort |
Q33853875 | Loss of Prox1 in striated muscle causes slow to fast skeletal muscle fiber conversion and dilated cardiomyopathy |
Q35151986 | Low rate of prenatal diagnosis among neonates with critical aortic stenosis: insight into the natural history in utero |
Q50979310 | MTHFD1 formyltetrahydrofolate synthetase deficiency, a model for the MTHFD1 R653Q variant, leads to congenital heart defects in mice. |
Q89442201 | Magnetic Resonance Imaging of Shear Stress and Wall Thickness in Tissue-Engineered Vascular Grafts |
Q38286183 | Management of atrial fibrillation in patients with congenital heart defects |
Q39102485 | Management of complex CHD at the National Cardiothoracic Center of Excellence, University of Nigeria Teaching Hospital, Enugu: the role of foreign cardiac missions in 3.5 years. |
Q38139299 | Management of pulmonic regurgitation and right ventricular dysfunction in the adult with repaired tetralogy of fallot |
Q92280600 | Maternal Body Mass Index and Risk of Congenital Heart Defects in Infants: A Dose-Response Meta-Analysis |
Q92702491 | Maternal Dietary Patterns during Pregnancy and Congenital Heart Defects: A Case-Control Study |
Q61798663 | Maternal LINE-1 DNA Methylation and Congenital Heart Defects in Down Syndrome |
Q64102976 | Maternal Viral Infection and Risk of Fetal Congenital Heart Diseases: A Meta-Analysis of Observational Studies |
Q42593923 | Maternal cigarette smoking and congenital heart defects |
Q89974256 | Maternal dietary fat intake and the risk of congenital heart defects in offspring |
Q37019059 | Maternal exposure to air pollutant PM2.5 and PM10 during pregnancy and risk of congenital heart defects |
Q47142165 | Maternal folic acid supplementation and dietary folate intake and congenital heart defects. |
Q42247538 | Maternal influenza-like illness, medication use during pregnancy and risk of congenital heart defects in offspring |
Q34282250 | Maternal obesity and tobacco use modify the impact of genetic variants on the occurrence of conotruncal heart defects |
Q92715024 | Maternal vitamin D level and vitamin D receptor gene polymorphism as a risk factor for congenital heart diseases in offspring; An Egyptian case-control study |
Q38872389 | Mechanism responsible for D-transposition of the great arteries: Is this part of the spectrum of right isomerism? |
Q39129349 | Mechanisms of Cardiomyocyte Proliferation and Differentiation in Development and Regeneration |
Q38022553 | Mechanotransduction in embryonic vascular development. |
Q41014050 | Mesodermal expression of Moz is necessary for cardiac septum development |
Q57170707 | Meta-Prediction of MTHFR Gene Polymorphism and Air Pollution on the Risks of Congenital Heart Defects Worldwide: A Transgenerational Analysis |
Q34341540 | MiRiad Roles for MicroRNAs in Cardiac Development and Regeneration |
Q91723017 | Micro-RNA signatures in monozygotic twins discordant for congenital heart defects |
Q35674144 | Micro-economic impact of congenital heart surgery: results of a prospective study from a limited-resource setting |
Q47932384 | MicroRNA expression, target genes, and signaling pathways in infants with a ventricular septal defect |
Q47314611 | MicroRNA-34a modulates the Notch signaling pathway in mice with congenital heart disease and its role in heart development |
Q35831338 | MicroRNA-375 overexpression influences P19 cell proliferation, apoptosis and differentiation through the Notch signaling pathway |
Q26770481 | MicroRNAs in congenital heart disease |
Q36754690 | Mild decrease in TBX20 promoter activity is a potentially protective factor against congenital heart defects in the Han Chinese population |
Q47098874 | Minimally invasive, multi-disciplinary approach for surgical management of a mediastinal congenital bronchogenic cyst in a 6-month-old infant. |
Q39840907 | Mortality and complications in 3495 children with isolated ventricular septal defects |
Q35944052 | Mortality from Congenital Heart Disease in Mexico: A Problem on the Rise |
Q53435475 | Mothers and Fathers Experience Stress of Congenital Heart Disease Differently: Recommendations for Pediatric Critical Care. |
Q43136777 | Mouse and human CRKL is dosage sensitive for cardiac outflow tract formation |
Q36921159 | Multicolor mapping of the cardiomyocyte proliferation dynamics that construct the atrium |
Q100738340 | Multiscale cardiac imaging spanning the whole heart and its internal cellular architecture in a small animal model |
Q93379589 | Mutations in EPAS1 in congenital heart disease in Tibetans |
Q43150752 | Myocardial Injury in Children with Unoperated Congenital Heart Diseases. |
Q97523676 | NOX2 Is Critical to Endocardial to Mesenchymal Transition and Heart Development |
Q37341787 | NT-proBNP and exercise capacity in adult patients with congenital heart disease and a prosthetic valve: a multicentre PROSTAVA study |
Q64098616 | Nationwide Increase in Complex Congenital Heart Diseases After the Fukushima Nuclear Accident |
Q101141379 | Next-Generation Sequencing in a Series of 80 Fetuses with Complex Cardiac Malformations and/or Heterotaxy |
Q89584499 | Nonopioid analgesics for perioperative and cardiac surgery pain in children: Current evidence and knowledge gaps |
Q36105326 | Normal ranges for fetal electrocardiogram values for the healthy fetus of 18-24 weeks of gestation: a prospective cohort study |
Q36351001 | Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallot |
Q91559690 | Novel mutations of AXIN2 identified in a Chinese Congenital Heart Disease Cohort |
Q59168457 | Nuchal translucency and cardiac abnormalities in euploid singleton pregnancies |
Q99631913 | Nursing Guidelines on Cardiac Surgery and Parents' Anxiety: Randomized Clinical Trial |
Q89659928 | Objective Assessment of Counselling for Fetal Heart Defects: An Interdisciplinary Multicenter Study |
Q53556083 | Obstructive heart defects associated with candidate genes, maternal obesity, and folic acid supplementation. |
Q92418814 | Oligogenic inheritance of a human heart disease involving a genetic modifier |
Q93140368 | Opinions of general and adult congenital heart disease cardiologists on care for adults with congenital heart disease in Belgium: a qualitative study |
Q35825057 | Oral Dexmedetomidine Versus Midazolam as Anesthetic Premedication in Children Undergoing Congenital Heart Surgery |
Q36193368 | Oral-health-related background factors and dental service utilisation among Sudanese children with and without a congenital heart defects |
Q37166202 | Organizational topology of brain and its relationship to ADHD in adolescents with d-transposition of the great arteries |
Q49679355 | Origins and consequences of congenital heart defects affecting the right ventricle |
Q48093262 | Outcome after prenatal and postnatal diagnosis of complex congenital heart defects and the influence of genetic anomalies |
Q33811743 | Outcome of cardiac surgery in patients with congenital heart disease in England between 1997 and 2015. |
Q37345721 | Ozone and Other Air Pollutants and the Risk of Congenital Heart Defects |
Q91597567 | PREVENTION-ACHD: PRospEctiVE study on implaNTable cardioverter-defibrillator therapy and suddeN cardiac death in Adults with Congenital Heart Disease; Rationale and Design |
Q38964066 | Parental and peer support in adolescents with a chronic condition: a typological approach and developmental implications |
Q39181776 | Parental experiences with a hospital-based bead programme for children with congenital heart disease. |
Q38943515 | Parental perceptions of congenital cardiovascular malformations in their children |
Q47561948 | Parental support, internalizing symptoms, perceived health status, and quality of life in adolescents with congenital heart disease: influences and reciprocal effects |
Q53823788 | Parents' Experiences of Caring for Their Child at the Time of Discharge After Cardiac Surgery and During the Postdischarge Period: Qualitative Study Using an Online Forum. |
Q57545086 | Parents� Experiences of Caring for Their Child at the Time of Discharge After Cardiac Surgery and During the Postdischarge Period: Qualitative Study Using an Online Forum (Preprint) |
Q64242470 | Patent Foramen Ovale Closure in 2019 |
Q91776487 | Paternal-age-related de novo mutations and risk for five disorders |
Q38726464 | Pediatric Nurses' Perception of Support for Families With Children With Congenital Heart Defects |
Q38419638 | Pediatric cardiac surgery in low- and middle-income countries or emerging economies: a continuing challenge |
Q34764317 | Performance of different scan protocols of fetal echocardiography in the diagnosis of fetal congenital heart disease: a systematic review and meta-analysis |
Q98780141 | Periconceptional use of cod liver oil, a vitamin D source, could decrease the risk of CHD in offspring |
Q38749764 | Personalised dosing of medicines for children |
Q39542210 | Personality traits, quality of life and perceived health in adolescents with congenital heart disease |
Q38926286 | Physical Activity and Sedentary Behavior in Children With Congenital Heart Disease. |
Q39255421 | Physical self-concept and its link to cardiopulmonary exercise tolerance among adolescents with mild congenital heart disease. |
Q38923110 | Placenta-related complications in women carrying a foetus with congenital heart disease |
Q37698095 | Population attributable danger of hereditary heart breaks. Risk factors among newborns in Yazd, Iran |
Q90729459 | Post-operative acute kidney injury is associated with a biomarker of acute brain injury after paediatric cardiac surgery |
Q91729797 | Post-operative blood loss is higher among African American neonates undergoing open-heart surgery with cardiopulmonary bypass for CHD |
Q91792693 | Potential association of long noncoding RNA HA117 with tetralogy of Fallot |
Q37053667 | Potential biomarkers for predicting outcomes in CABG cardiothoracic surgeries |
Q99596927 | Pregnancy and early post-natal outcomes of fetuses with functionally univentricular heart in a low-and-middle-income country |
Q40533596 | Pregnancy complications in singleton pregnancies with isolated fetal heart defects |
Q52623794 | Pregnancy management and outcome in patients with four different tetrahydrobiopterin disorders. |
Q34526554 | Prematurity, asphyxia and congenital malformations underrepresented among neonates in a tertiary pediatric hospital in Vietnam |
Q35674107 | Prenatal Alcohol Exposure and Congenital Heart Defects: A Meta-Analysis |
Q91735674 | Prenatal detection of fetal heart disease at Jordan University Hospital: early experience in a developing country |
Q91075896 | Prenatal diagnosis and planned peri-partum care as a strategy to improve pre-operative status in neonates with critical CHDs in low-resource settings: a prospective study |
Q49887639 | Prenatal diagnosis of congenital heart disease: A review of current knowledge |
Q52855131 | Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with ventricular septal defects by chromosomal microarray-based analysis. |
Q50577401 | Prenatal identification of CHD murmur using four segment phonocardiographic signal analysis. |
Q33586243 | Presence of plaque, gingivitis and caries in Sudanese children with congenital heart defects |
Q38844848 | Prevalence and composition of CHD at different altitudes in Tibet: a cross-sectional study |
Q57215209 | Prevalence and mortality of congenital heart disease in Korean adults |
Q36188645 | Prevalence of Congenital Anomalies in an Indian Maternal Cohort: Healthcare, Prevention, and Surveillance Implications |
Q33646676 | Prevalence of Congenital Heart Disease among Infants from 2012 to 2014 in Langfang, China |
Q35758646 | Prevalence of Congenital Heart Disease in Xinjiang Multi-Ethnic Region of China |
Q46720545 | Prevalence of congenital heart disease |
Q49112073 | Prevalence of congenital heart disease among Palestinian children born in the Gaza Strip |
Q45070803 | Prevalence of congenital heart disease at live birth: an accurate assessment by echocardiographic screening |
Q44464735 | Prevalence of congenital heart diseases in Koranic schools (daara) in Dakar: a cross-sectional study based on clinical and echocardiographic screening in 2019 school children |
Q35762869 | Prognosis and Risk Factors for Congenital Airway Anomalies in Children with Congenital Heart Disease: A Nationwide Population-Based Study in Taiwan |
Q55439640 | Prognostic Value of Serial N-Terminal Pro-B-Type Natriuretic Peptide Measurements in Adults With Congenital Heart Disease. |
Q92016214 | Prognostic value of perioperative NT-proBNP after corrective surgery for pediatric congenital heart defects |
Q48522487 | Programmatic Changes to Reduce Mortality and Morbidity in Humanitarian Congenital Cardiac Surgery |
Q36165092 | Projected growth of the adult congenital heart disease population in the United States to 2050: an integrative systems modeling approach |
Q37560116 | Proportion of selected congenital heart defects attributable to recognized risk factors |
Q24202884 | Psychological interventions for depression in adolescent and adult congenital heart disease |
Q57154579 | Psychosocial functioning of parents of children with heart disease-describing the landscape |
Q28085572 | Pulmonary arterial hypertension associated with congenital heart disease and Eisenmenger syndrome: current practice in pediatrics |
Q87774893 | Pulmonic regurgitation and management challenges in the adult with tetralogy of fallot |
Q41188681 | Pulse oximetry as a screening tool for detecting major congenital heart defects in Indian newborns. |
Q47239461 | Pulse oximetry screening for critical congenital heart diseases at two different hospital settings in Thailand |
Q56431330 | Pulse oximetry with clinical assessment to screen for congenital heart disease in neonates in China: a prospective study |
Q92451424 | Quality of life in children with infrequent congenital heart defects: cohort study with one-year of follow-up |
Q49375799 | RCAN1 Mutation and Functional Characterization in Children with Sporadic Congenital Heart Disease |
Q61984925 | RETRACTED: Transcatheter Decellularized Tissue-Engineered Heart Valve (dTEHV) Grown on Polyglycolic Acid (PGA) Scaffold Coated with P4HB Shows Improved Functionality over 52 Weeks due to Polyether-Ether-Ketone (PEEK) Insert |
Q55155036 | Rapid Left Ventricular Recovery After Correction of a Secundum Atrial Septal Defect: Understanding the Hemodynamics. |
Q39608817 | Rare novel variants in the ZIC3 gene cause X-linked heterotaxy |
Q91699826 | Real-world healthcare utilization in adult congenital heart disease: a systematic review of trends and ratios |
Q58562094 | Recent advances and challenges on application of tissue engineering for treatment of congenital heart disease |
Q91829490 | Reduced maternal vitamin A status increases the incidence of normal aortic arch variants |
Q36259472 | Regression equations for calculation of z scores for echocardiographic measurements of right heart structures in healthy Han Chinese children |
Q92445859 | Reiterative Mechanisms of Retinoic Acid Signaling during Vertebrate Heart Development |
Q35054966 | Relationship of white matter network topology and cognitive outcome in adolescents with d-transposition of the great arteries |
Q35825746 | Remote Ischemic Preconditioning Fails to Benefit Pediatric Patients Undergoing Congenital Cardiac Surgery: A Meta-Analysis of Randomized Controlled Trials |
Q34172585 | Replication of the 4p16 susceptibility locus in congenital heart disease in Han Chinese populations |
Q38955826 | Representativeness of the German National Register for Congenital Heart Defects: a clinically oriented analysis |
Q38044069 | Resuscitation and perioperative management of the high-risk single ventricle patient: first-stage palliation |
Q91654730 | Right anterolateral mini-thoracotomy without inferior vena cava cannulation for atrial septal defect repair in small children: A feasible technique |
Q41491119 | Right atrial isomerism in children older than 3 years |
Q91922137 | Risk Factors for Major Adverse Events after Surgical Closure of Ventricular Septal Defect in Patients Less than 1 Year of Age: A Single-Center Retrospective |
Q104134104 | Risk factors and lifelong impact of community-acquired pneumonia in congenital heart disease |
Q102055053 | Risk factors for severe pulmonary regurgitation after repair of tetralogy of Fallot with transannular patch |
Q37580544 | Risk of Congenital Heart Defects after Ambient Heat Exposure Early in Pregnancy. |
Q37672388 | Risk of necrotizing enterocolitis in very-low-birth-weight infants with isolated atrial and ventricular septal defects |
Q47123245 | Role of dual source multidetector row cardiac computed tomography angiography in diagnosis and management of congenital heart disease patients |
Q55315254 | Role of pulmonary hemodynamics in determining 6-minute walk test result in atrial septal defect: an observational study. |
Q47221722 | S-Nitrosohemoglobin Levels and Patient Outcome After Transfusion During Pediatric Bypass Surgery |
Q38985712 | Safety and efficacy of transthoracic versus transesophageal echocardiography in transcatheter closure of atrial septal defects. Reporting a single center experience from Saudi Arabia |
Q38894389 | School-related adjustment in children and adolescents with CHD. |
Q34472248 | Secundum atrial septal defect in adults: a practical review and recent developments |
Q40269799 | Sense of coherence does not moderate the relationship between the perceived impact of stress on health and self-rated health in adults with congenital heart disease |
Q35867362 | Serum Bile Acids in Repaired Tetralogy of Fallot: A Marker for Liver and Heart? |
Q36587094 | Serum NT-proBNP Levels Are Not Related to Vitamin D Status in Young Patients with Congenital Heart Defects |
Q47137544 | Short-term outcomes of transcatheter closure of secundum atrial septal defect in children and adolescents: An experience of two centers in Upper Egypt |
Q48847616 | Shunt flow evaluation in congenital heart disease based on two-dimensional speckle tracking |
Q37527752 | Sickle Cell Disease with Cyanotic Congenital Heart Disease: Long-Term Outcomes in 5 Children |
Q37297481 | Silencing of TBX20 gene expression in rat myocardial and human embryonic kidney cells leads to cell cycle arrest in G2 phase |
Q38921431 | Silencing of nodal modulator 1 inhibits the differentiation of P19 cells into cardiomyocytes |
Q89523122 | Simulation of semilunar valve function: computer-aided design, 3D printing and flow assessment with MR |
Q90259607 | Single centre audit of early impact of inclusion of the three vessel and trachea view in obstetric screening |
Q58119737 | Social Risk Factors Impact Hospital Readmission and Outpatient Appointment Adherence for Children with Congenital Heart Disease |
Q33813900 | Spatial patterns of the congenital heart disease prevalence among 0- to 14-year-old children in Sichuan Basin, P. R China, from 2004 to 2009. |
Q91967616 | Spectrum of heart diseases in children presenting to a paediatric cardiac echocardiography clinic in the Lake Zone of Tanzania: a 7 years overview |
Q36516393 | Spectrum of heart diseases in children: an echocardiographic study of 1,666 subjects in a pediatric hospital, Yaounde, Cameroon |
Q52603570 | Spontaneous Closure of a Secundum Atrial Septal Defect. |
Q90372470 | Standard median sternotomy, right minithoracotomy, totally thoracoscopic surgery, percutaneous closure, and transthoracic closure for atrial septal defects in children: A protocol for a network meta-analysis |
Q64104201 | Status of Pediatric Cardiac Care in Developing Countries |
Q92742846 | Study on the Potential Biomarkers of Maternal Urine Metabolomics for Fetus with Congenital Heart Diseases Based on Modified Gas Chromatograph-Mass Spectrometer |
Q89506173 | Successful simultaneous transcatheter treatment for a secundum atrial septal defect complicated by valvular pulmonary stenosis in an infant |
Q55417728 | Suggestion of reduced cancer risks following cardiac x-ray exposures is unconvincing. |
Q26853302 | Surgical Interventions for Congenital Anomalies |
Q91793518 | Surgical outcomes in complex adult congenital heart disease: a brief review |
Q41835875 | Surgical repair of tricuspid valve leaflet tear following percutaneous closure of perimembranous ventricular septal defect using Amplatzer duct occluder I: Report of two cases |
Q40454793 | Surveillance of ventricular septal defects in Delaware. |
Q35046926 | Synopsis of congenital cardiac disease among children attending University of Nigeria Teaching Hospital Ituku Ozalla, Enugu |
Q47671876 | Systematic review and meta-analysis of the performance of second-trimester screening for prenatal detection of congenital heart defects |
Q33702965 | TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus |
Q50770648 | TCF21 rs12190287 Polymorphisms Are Associated with Ventricular Septal Defects in a Chinese Population. |
Q36632187 | Tachyarrhythmia in patients with congenital heart disease: inevitable destiny? |
Q27318593 | Targeted inactivation of Cerberus like-2 leads to left ventricular cardiac hyperplasia and systolic dysfunction in the mouse |
Q52679852 | Tell me once, tell me soon: parents' preferences for clinical genetics services for congenital heart disease. |
Q38645644 | Template-based Quality Assessment of the Doppler Ultrasound Signal for Fetal Monitoring |
Q64039584 | Tetralogy of Fallot in Spain: a nationwide registry-based mortality study across 36 years |
Q34658128 | Texting teens in transition: the use of text messages in clinical intervention research |
Q37303132 | The Burden of Care: Mothers' Experiences of Children with Congenital Heart Disease |
Q33608215 | The Changing Landscape of Pulmonary Arterial Hypertension in the Adult with Congenital Heart Disease |
Q48206400 | The Congenital Heart Disease Genetic Network Study: Cohort description |
Q38992606 | The Effect of Endothelin Receptor Antagonists in Patients with Eisenmenger Syndrome: A Systematic Review |
Q64904288 | The Effect of Multidisciplinary Approach on the Birth Rate of Fetuses with Prenatally Diagnosed Congenital Heart Disease. |
Q92342856 | The Evolution of Tissue Engineered Vascular Graft Technologies: From Preclinical Trials to Advancing Patient Care |
Q91893921 | The Experiences of Parents of Children Undergoing Surgery for Congenital Heart Defects: A Holistic Model of Care |
Q52646155 | The MALAT1 gene polymorphism and its relationship with the onset of congenital heart disease in Chinese. |
Q55313445 | The Need for Specialized Pediatric Cardiac Critical Care Training Program in Limited Resource Settings. |
Q90674148 | The Outcome of Prenatally Diagnosed Isolated Fetal Ventricular Septal Defect |
Q64112163 | The Pediatric Cell Atlas: Defining the Growth Phase of Human Development at Single-Cell Resolution |
Q64070763 | The Predictive Value of Infant-Specific Preoperative Pulmonary Function Tests in Postoperative Pulmonary Complications in Infants with Congenital Heart Diseases |
Q96137125 | The Prevalence of Congenital Heart Diseases in Syndromic Children at King Khalid National Guard Hospital from 2005 to 2016 |
Q26741187 | The Risk of Congenital Heart Anomalies Following Prenatal Exposure to Serotonin Reuptake Inhibitors-Is Pharmacogenetics the Key? |
Q58797144 | The Role of Abnormal Placentation in Congenital Heart Disease; Cause, Correlate, or Consequence? |
Q55289365 | The Role of Clinical Psychology and Peer to Peer Support in the Management of Chronic Medical Conditions - A Practical Example With Adults With Congenital Heart Disease. |
Q90620561 | The Spectrum of Pediatric Cardiac Procedures and Their Outcomes: A Six-month Report from the Largest Cardiac Facility in Sindh, Pakistan |
Q34124815 | The association between brain injury, perioperative anesthetic exposure, and 12-month neurodevelopmental outcomes after neonatal cardiac surgery: a retrospective cohort study |
Q50118816 | The association between maternal exposure to pollutant particulate matter 2.5 and neonatal congenital heart defects: a systematic review protocol |
Q64939423 | The association of elevated maternal genetic risk scores for hypertension, type 2 diabetes and obesity and having a child with a congenital heart defect. |
Q52888439 | The association of maternal lymphatic markers and critical congenital heart defects in the fetus-A population based case-control study. |
Q46302230 | The current status and future of cardiac stem/progenitor cell therapy for congenital heart defects from diabetic pregnancy |
Q55228367 | The development of a consensus-based nutritional pathway for infants with CHD before surgery using a modified Delphi process. |
Q90460684 | The eye in CHD |
Q50742524 | The genotype and expression of the TGFβ2 gene in children with congenital conotruncal defects. |
Q46092374 | The global burden of paediatric heart disease |
Q36854388 | The impact of congenital heart diseases on the quality of life of patients and their families in Saudi Arabia. Biological, psychological, and social dimensions |
Q33894532 | The importance of copy number variation in congenital heart disease |
Q38814400 | The importance of early involvement of paediatric palliative care for patients with severe congenital heart disease |
Q33858937 | The importance of small for gestational age in the risk assessment of infants with critical congenital heart disease |
Q40389769 | The influence of maternal exposure history to virus and medicine during pregnancy on congenital heart defects of fetus |
Q89006973 | The invisible child: childhood heart disease in global health |
Q39000709 | The prevalence of congenital heart defects in infants with cholestatic disorders of infancy: a single-centre study. |
Q93271168 | The prevalence of genetic diagnoses in fetuses with severe congenital heart defects |
Q37681889 | The pro-inflammatory signalling regulator Stat4 promotes vasculogenesis of great vessels derived from endothelial precursors |
Q38888906 | The renin-angiotensin-aldosterone-system and right heart failure in congenital heart disease |
Q35113038 | The risk of cancer in patients with congenital heart disease: a nationwide population-based cohort study in Taiwan |
Q104288208 | The screening of congenital heart disease by cardiac auscultation and 12-lead electrocardiogram among Indonesian elementary school students |
Q39198996 | The single-ventricle patient population: a current and future concern a population-based study in the North of England |
Q61795962 | The ubiquitin ligase HECTD1 promotes retinoic acid signaling required for development of the aortic arch |
Q40625334 | The unnatural history of pulmonary stenosis up to 40 years after surgical repair |
Q38045087 | The usefulness of brain natriuretic peptide in simple congenital heart disease - a systematic review |
Q38768390 | Three- and four-dimensional ultrasound in fetal echocardiography: an up-to-date overview |
Q51606000 | Three-Dimensional Echocardiography in the Evaluation of Right Ventricular Global and Regional Systolic Function in Patients with Atrial Septal Defect before and after Percutaneous Closure. |
Q38310446 | Three-dimensional echocardiographic assessment of atrial septal defects |
Q49907216 | Three-dimensional printing in congenital heart disease: A systematic review |
Q90455769 | Timing of pulmonary valve replacement in patients with corrected Fallot to prevent QRS prolongation |
Q94465779 | Tissue Engineered Materials in Cardiovascular Surgery: The Surgeon's Perspective |
Q55057914 | Tissue engineered vascular grafts for pediatric cardiac surgery. |
Q47868970 | Tissue-engineered vascular grafts for congenital cardiac disease: Clinical experience and current status |
Q28075811 | Top 100 cited articles in cardiovascular magnetic resonance: a bibliometric analysis |
Q49657811 | Totally Endoscopic Cardiac Surgery for Atrial Septal Defect Repair on Beating Heart Without Robotic Assistance in 25 Patients. |
Q53059111 | Toward computer-assisted image-guided congenital heart defect repair: an initial phantom analysis. |
Q34211932 | Tracheostomy in children with congenital heart disease: a national analysis of the Kids' Inpatient Database |
Q33840353 | Transcriptional atlas of cardiogenesis maps congenital heart disease interactome |
Q92559978 | Transcriptome analysis defines myocardium gene signatures in children with ToF and ASD and reveals disease-specific molecular reprogramming in response to surgery with cardiopulmonary bypass |
Q48509176 | Translation and Testing of the Swedish Version of Iceland-Family Perceived Support Questionnaire With Parents of Children With Congenital Heart Defects |
Q39037706 | Transposition of the Great Arteries in the Developing World: Surgery and Outcomes |
Q37023891 | Treatment of heart failure in adult congenital heart disease: a position paper of the Working Group of Grown-Up Congenital Heart Disease and the Heart Failure Association of the European Society of Cardiology |
Q41130704 | Trends in Mortality of Congenital Heart Defects |
Q89506133 | Trends in prescription of cardiovascular drugs to children in relation to prevalence of CHD from 1999 to 2016 |
Q55113834 | Trends in the Prevalences of Selected Birth Defects in Korea (2008⁻2014). |
Q55438930 | Truncus arteriosus communis: report of three cases and review of literature. |
Q38759697 | Type 1 diabetes mellitus and associated risk factors in patients with or without CHD: a case-control study |
Q104134385 | Ultrahigh-Frequency Echocardiography of Autonomic Devoid Phox2B Homozygous Embryos Does Not Reveal a Significant Cardiac Phenotype before Embryo Death |
Q26747417 | Universal Pulse Oximetry Screening for Early Detection of Critical Congenital Heart Disease |
Q94541561 | Update of genetic variants in the NKX2-5 gene |
Q38935028 | Use of hierarchical models to analyze European trends in congenital anomaly prevalence |
Q33606002 | Validity and reliability of the Physical Activity Questionnaire for Children (PAQ-C) and Adolescents (PAQ-A) in individuals with congenital heart disease |
Q54290731 | Variability of Myocardial Repolarization in Pediatric Patients with a Ventricular Septal Defect. |
Q35961039 | Variants in the Regulatory Region of WNT5A Reduced Risk of Cardiac Conotruncal Malformations in the Chinese Population. |
Q42862095 | Variations of pulmonary arteries and other associated defects in Tetralogy of Fallot |
Q91788802 | Venous thromboembolism in chronic pediatric heart disease is associated with substantial health care burden and expenditures |
Q48423624 | Ventricular myocardial deformation in adults after early surgical repair of atrial septal defect |
Q91529015 | Versican is crucial for the initiation of cardiovascular lumen development in medaka (Oryzias latipes) |
Q53171659 | Virtual autopsy by computed tomographic angiography of the fetal heart: a feasibility study. |
Q58590909 | WDR5 regulates left-right patterning via chromatin dependent and independent functions |
Q47128713 | Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns |
Q50026226 | Wie Eltern und ihre Kinder die pflegegeleitete Transitionssprechstunde für Adoleszente mit angeborenen Herzfehlern erleben |
Q30239747 | Worldwide prevalence of adverse pregnancy outcomes among singleton pregnancies after in vitro fertilization/intracytoplasmic sperm injection: a systematic review and meta-analysis |
Q30238510 | Worldwide prevalence of adverse pregnancy outcomes associated with in vitro fertilization/intracytoplasmic sperm injection among multiple births: a systematic review and meta-analysis based on cohort studies |
Q36733249 | Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxy |
Q92649614 | Xenopus: Driving the Discovery of Novel Genes in Patient Disease and Their Underlying Pathological Mechanisms Relevant for Organogenesis |
Q52412927 | [Research advances in the mechanism of congenital heart disease induced by pregestational diabetes mellitus]. |