Feasibility of atrial septal defect type II occluders determined by computed tomography virtual cardioscope.

Late Diagnosis of Unroofed Coronary Sinus Associated with Persistent Left Superior Vena Cava in Patient with Repaired Tetralogy of Fallot: Case Report.

ROBO2 Variants Associated With Atrial Septal Defect Define a Novel Regulatory Element.

Percutaneous closure of an ultra-long-tunnel-type patent foramen ovale: a rare case with multimodal imaging guidance.

Outcome in Patients with Secundum Type Atrial Septal Defect Referred for Percutaneous or Surgical Closure: A Single-Center Experience.

Anaesthetic Management of a Case of Minimally Invasive Surgical Repair of Sinus Venosus Atrial Septal Defect (SVASD) and Persistent Left Superior Vena Cava (LSVC), Assisted by Unique Bilateral Percutaneous Superior Vena Cava Cannulation.

Paradoxical air embolism in patient with patent foramen ovale during liver transplant.

Atrial septal pouch: a comprehensive morphologic and morphometric evaluation with clinical relevance.

Single incision minimally invasive congenital heart surgery: Insights into program development and outcome.

Case Report: Concurrent atrial and ventricular septal defect in a young Sphynx cat.

Machine learning-based predictive model for atrial arrhythmia following transcatheter atrial septal defect closure.

The relation between Down syndrome and co-occurring conditions in children and young adults: A population-based cohort in Denmark, 1977-2016.

Follow-Up of Neonatally Diagnosed Atrial Septal Defects and Patent Foramen Ovale at Preschool Age.

Beyond the murmur: unmasking a rare sinus venosus ASD in an adolescent with chronic respiratory infections: A case report.

Development of a 3D-printed canine cardiac disease model for interventional procedure training.

Biventricular Interatrial Shunt With Desaturation After Atrial Septal Defect Repair.

Long-term outcomes of Eisenmenger syndrome in the era of targeted pulmonary vasodilator therapy.

Multisystem Phenotypic Spectrum in Pediatric Heterotaxy Syndrome: A Case Series.

From Catheter Complication to Surgical Success: Urgent Retrieval of an Embolized Amplatzer Device and Valve Repair.

A Rare Case of Chronic Thromboembolic Pulmonary Hypertension in an Elderly With Atrial Septal Defect and Eisenmenger Syndrome.

Transcatheter closure of ostium secundum atrial septal defects in 2253 children and adults: Early outcomes.

The deficiency of DIP2C leads to congenital heart defects in patients with 10p15.3 microdeletion syndrome.

Prevalence, classification, and treatment of residual shunt after patent foramen ovale closure.

A case of anomalous right coronary artery from the pulmonary trunk, aortopulmonary window, and interrupted aortic arch type a in a term neonate.

Incidence, Associated Abnormalities, and Outcomes of Dextrocardia: A Registry-based Study in Saudi Arabia.

The relationship of NOS3 G894 T (rs1799983) gene polymorphism in the risk of congenital heart disease: a meta-analysis and bioinformatics study.

Mitral and tricuspid valve repair in an operated case of complete atrioventricular septal defect: A surgical challenge case report!

PFO closure in a patient with hypoxia due to tricuspid valve regurgitation and flow-driven shunt.

Assessment of tricuspid annulus geometry in children with congenital heart disease using three-dimensional echocardiography.

Open atrial septal defect repair in a dog using fresh autologous pericardium.

Mixed Inferior Sinus Venosus and Secundum Atrial Septal Defects with Mixed Partial Anomalous Pulmonary and Systemic Venous Drainage: Key Insights and Practical Implications.

Case Report: Thoracoscopic repair of a residual inferior sinus venosus-type defect with right lower pulmonary vein-inferior vena cava communication: intraoperative support using real-time 3D transesophageal echocardiography.

The association analysis between Glucose-6-Phosphate dehydrogenase deficiency and susceptibility to common diseases in children.

Focal Dermal Hypoplasia with Unusual Cardiac Anomalies Presentation: A Report of Two Cases and Literature Review.

Genome-Wide Association Studies of Down Syndrome Associated Congenital Heart Defects Suggests a Genetically Heterogeneous Risk for CHD in DS.

Successful experience of transcatheter residual right-to-left shunting closure after patent foramen ovale occlusion.

Clarifying the cardiovascular morphology and associated abnormalities in patients with tricuspid Atresia using multidetector computed tomography angiography.

Quantitative Volumetric Analysis of the Patent Foramen Ovale Tunnel in Coronary Computed Tomography Angiography: Clinical Implications and Diagnostic Significance.

Current Trends in Device and Size Selection for Transcatheter Atrial Septal Defect Closure in Adults　- Insights From a Japanese Nationwide Registry.

Risk factor analysis for cardiac abnormalities in patients with idiopathic scoliosis.

Update on the Clinical and Molecular Characterization of Noonan Syndrome and Other RASopathies: A Retrospective Study and Systematic Review.

[Finite Element Simulation Analysis of a Nickel-Titanium Alloy Patent Foramen Ovale Occluder].

Invasive management of unroofed coronary sinus: A systematic review.

Safety and one-year follow-up analysis of percutaneous ASD closure at a tertiary care hospital.

Hemodynamic Changes After Wire Frame Occluders vs. Metal Mesh Devices for Atrial Septal Defect.

Characteristics and postoperational outcomes in paediatric patients with coronary sinus septal defect: a retrospective cohort study.

Association of atrial cardiopathy and residual shunt after patent foramen ovale closure in patients experiencing migraine.

Performance against standardization recommendations for outpatient care of common forms of congenital heart disease.

A Comparison of Long-Term Right Ventricular Functions in Children with Transcatheter and Surgically Closed Secundum Atrial Septal Defects (ASDs): A Strain Echocardiography Study.

Prevalence of scoliosis and congenital heart disease based on school screening in Jinghong City, Yunnan Province.

National practice patterns for the use of regional anesthesia for pediatric cardiac surgery: An analysis of the Society of Thoracic Surgeons congenital heart surgery database.

Clarifying the Cardiovascular Morphology and Associated Abnormalities in Patients with Double Inlet Right Ventricle Using Multidetector CT Angiography.

Evaluation of short-term consequences of atrial septal defect closure in adults referred to Shahid Chamran heart center in Isfahan.

Bilateral thalamic infarction with posterior cerebral artery variant (the arcade artery): A case report.

Prevalence of Congenital Heart Disease in Children and Adolescents Under 18 in Africa: A Systematic Review and Meta-Analysis.

[Immediate outcomes of simultaneous Cox-Maze procedure in patients with isolated and multivalvular heart defects via right mini-thoracotomy].

Epidemiology of Congenital Heart Defects in Perinatal Infants in Guangxi, China.

Case presentation: successful occlusion of congenital left ventricle to coronary sinus fistula.

Paradoxical cerebral embolism caused by patent foramen ovale in a patient with multiple endocrine neoplasia type 1 and severe primary hyperparathyroidism.

Thoracoscopic closure of atrial septal defect in perfused beating hearts.

COMPARATIVE ANALYSIS OF THE CLINICAL RESULTS OF PATIENTS WITH ASD OPERATED VIA RIGHT ANTERIOR MINITHORACOTOMY AND MEDIAN STERNOTOMY.

Double innominate vein in a case with double aortic arch: a case report.

Influence of procedural timing on the preventive yield of percutaneous patent foramen ovale closure.

2q31 microdeletion syndrome with the velocardiofacial phenotype and review of the literature: a case report.

Echocardiography-guided percutaneous closure of oval-shaped secundum atrial septal defects.

Missense mutations in the CITED2 gene may contribute to congenital heart disease.

Long-Term Results of the Atrial Septal Defect Occluder ASSURED Trial for Combined Pivotal/Continued Access Cohorts.

Ischemic Stroke in Adults With Congenital Heart Disease: Cumulative Incidence and Associated Factors.

Genome-wide association studies of Down syndrome associated congenital heart defects.

Functional characterization vs in silico prediction for TBX5 missense and splice variants in Holt-Oram syndrome.

Diagnosis of Congenital Heart Disease in Adulthood: How Often, How Relevant?

Snare device retrieval of occluder embolized in patent foramen ovale closure: A case report.

Epidemiology of paediatric chronic heart failure in Germany-A population-based analysis.

Interatrial Septum Assessment by Transthoracic Echocardiography Part 1: Secundum ASD.

A very rare fetal echocardiography diagnosis: Sinus venosus type atrial septal defect with pulmonary venous return abnormality.

Holt-Oram Syndrome With Atrial Septal Defect.

Antithrombotic Therapy Following Structural Heart Disease Interventions: Current Status and Future Directions.

Recent Development of Biodegradable Occlusion Devices for Intra-Atrial Shunts.

Atrial Septal Defect (ASD) Repair Unveiling an Unusual Conduction Conundrum: A Wenckebach Case Report.

Association between patent foramen ovale morphology and clinical outcomes following transcatheter closure.

Complex ADHD Challenging Case: Managing Co-Occurring Attention-Deficit Hyperactivity Disorder and Congenital Heart Disease with a Limited Medication Formulary: A Case from Mexico.

Three-dimensional transesophageal echocardiography measurements of ASD sizing parameters in comparison to balloon sizing method in percutaneous ASD closure.

The association of right ventricular-pulmonary arterial coupling and pulmonary vascular resistance in adult patients with uncorrected atrial septal defect.

Age-Related Variations in Patterns of Patent Foramen Ovale-Stroke versus Other Cryptogenic Stroke.

Does this child just have an atrial septal defect? More potentiality of interventional therapy: A rare case report.

Left ventricle-right atrial communication: A specific type of ventricular septal defect.

Infant Barlow's Disease in Association with Atrial Septal Defect.

Interventional heart catheterization to close atrial septal defect, patent ductus arteriosus, ventricular septal defect in a 3.5-year-old girl; a case report study.

Co-occurrence of patent foramen ovale and Chiari network in a diabetic patient.

Atrial Septal Abnormalities and Cryptogenic Stroke: A Cross-Sectional Study.

Illuminating the Genetic Basis of Congenital Heart Disease in Patients with Kabuki Syndrome.

Complications and Efficacies of Surgical Versus Transcatheter Closure for Pediatric Ostium Secundum Atrial Septal Defect: A Meta-Analysis.

Antithrombin deficiency caused by SERPINC1 gene mutation in white matter lesions: A case report.

Headache patterns in patent foramen ovale patients: beyond migraine with aura.

Risk factors for isolated atrial septal defect secundum morbidity.

Complete free wall isolation of arrhythmogenic persistent left superior vena cava.

Cerebral Embolism and MINOCA Secondary to Left Atrial Myxoma after Occlusion of Atrial Septal Defect by Amplatzer Occluder: A Case Report.

Calmodulin mutation in long QT syndrome 15 associated with congenital heart defects further complicated by a functional 2:1 atrioventricular block: Management from foetal life to postpartum.

Left Atrial Stiffness Increases after Trans-Catheter Atrial Septal Closure.

Type-I umbilical-systemic shunt with abnormal connection to azygos vein in fetus with de-novo TBX5 mutation related to Holt-Oram syndrome.

Comparative evaluation of microprobe versus conventional transoesophageal echocardiography for PFO closure guidance.

Amplatzer Vascular Plug closure of an iatrogenic interatrial tunnel-type communication.

Lutembacher's Syndrome Accompanied by Partial Anomalies of Pulmonary Veins in a 70-Year-Old Male: A Case of Congenital Heart Disease in the Elderly.

Case report: Amplatzer septal occluder device migration into the descending thoracic aortic isthmus: percutaneous retrieval and redeployment.

[An unexpected case of right heart dilation in the elderly].

Cor triatriatum sinister with dextrocardia in association with ostium secundum atrial septal defect, subpulmonary ventricular septal defect and bicuspid pulmonary valve in a pig.

Long-term follow-up of percutaneous secundum-type atrial septal defect closure using Amplatzer Septal Occluder since 1995: a single-centre study.

Comparing apples to apples: Exploring public reporting of congenital cardiac surgery outcomes based on common congenital heart operations.

Elevated risk for developmental disabilities in children with congenital heart defects.

Maternal Blood Group Is a Possible Predictor for Developing Congenital Heart Disease in Turkish Children with Down's Syndrome.

Congenital Heart Defects and Outcome in a Large Cohort of Down Syndrome: A Single-Center Experience from Turkey.

Case report: A unique quadruple coexisting anomaly-scimitar syndrome, atrial septal defect, vascular ring, and pulmonary sequestration.

New-onset atrial fibrillation after percutaneous patent foramen ovale closure: a meta-analysis.

15q26.3 deletions distal to IGF1R cause growth retardation, congenital heart defect and skeletal anomalies: Case report and review of literature.

Atrial Septal Defect: Larger Right Ventricular Dimensions and Atrial Volumes as Early as in the First Month After Birth-a Case-Control Study Including 716 Neonates.

Left atrial disc device thrombosis after atrial defect closure with the Gore® Cardioform septal occluder: A case series.

Incidence of cardiac anomalies in congenital vertebral deformity: systematic review and meta-analysis of 2910 patients.

Effects of morphological characteristics of patent foramen ovale by transesophageal echocardiography on minimalist transcatheter closure in southern China.

Caroli syndrome associated with atrial septal defect and polydactyly: a case report.

Prevalence and Associated Factors of Congenital Heart Disease in Cleft Lip and Palate Patients at the University of Benin Teaching Hospital.

Clinical utility of repeat fetal echocardiography in congenital heart disease.

A Single Center Observational Study of Spirometry Assessments in Children with Congenital Heart Disease after Surgery.

Extra-cardiac and complex Fontan baffle fenestration using radio frequency current via surgical electrocautery.

Echocardiographic right ventricular remodeling after percutaneous atrial septal defect closure.

Unrecognized Patent Foramen Ovale in Patient With Sinus Venosus-Type Atrial Septal Defect With Partial Anomalous Pulmonary Venous Return.

Effect of percutaneous closure on atrium and appendage functions in patients with secundum atrial septal defects.

When a Hypersomnolent Hemodialyzed Patient Actually Has a Rare Stroke: A Case of Artery of Percheron Infarction With Paradoxical Embolism.

Percutaneous Treatment of Left Main Coronary Artery Compression in a Pulmonary Artery Hypertension Patient Associated with Atrial Septal Defect.

The relationship between echocardiographic parameters and albumin bilirubin (ALBI) score in patients with isolated secundum type atrial septal defect.

Cardiac anomalies in children with congenital duodenal obstruction: a systematic review with meta-analysis.

Impact of the antiplatelet strategy following patent foramen ovale percutaneous closure.

The Need for Surgery After Vascular or Cardiac Trauma, or Technical Adverse Events in the Congenital Cardiac Catheterization Laboratory.

Catheter ablation of left atrial tachycardia adjacent to a septal closure device: A multifaceted challenge?

Outcome of transcatheter atrial septal defect closure in a nationwide cohort.

Surgical correction of a ventricular septal defect in a child with spinal muscular atrophy type 2 treated with nusinersen sodium: a case report.

Sufficient versus deficient rims during percutaneous closure of ostium secundum type atrial septal defect: A systematic review and meta-analysis.

The Yasui procedure with a modified right ventricle-to-pulmonary artery connection utilizing autologous left atrial appendage as a free graft.

Massively Hypertrophied Right-Sided Heart with Hypoplastic Left-Sided Heart in a Neonate (A Rare Type of Hypertrophic Cardiomyopathy).

Augmented detection of septal defects using advanced optical coherence tomography network-processed phonocardiogram.

The value of cardiac CT in the diagnosis of unroofed coronary sinus syndrome.

Neonatal mortality and morbidity in Down syndrome in the time of prenatal aneuploidy testing: a retrospective cohort study.

The anomalous drainage of the inferior vena cava into the left atrium.

Trans-catheter closure of ASD and abnormal connection of left pulmonary vein to vertical vein: A case report.

Multimodality imaging approach of patent foramen ovale: Practical considerations for transient ischemic attack/stroke.

Transcatheter Atrial Septal Defect Closure Before Versus After Adulthood.

Identification and functional analysis of genetic variants of ISL1 gene promoter in human atrial septal defects.

Transcatheter Closure of Patent Foramen Ovale in Patients With Peripheral (Noncerebrovascular) Embolism.

Surgical correction of total anomalous pulmonary venous return in an adult patient.

Transcatheter retrieval of atrial septal defect and patent ductus arteriosus occluder: a guidance for device retrieval based on comprehensive bench tests.

Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome.

Catheter Ablation for Atrial Fibrillation in Adult Congenital Heart Disease: An International Multicenter Registry Study.

Monitoring for atrial fibrillation prior to patent foramen ovale closure after cryptogenic stroke.

Concomitant cardiovascular malformations in isolated bicuspid aortic valve disease: a retrospective cross-sectional study and meta-analysis.

Transcatheter closure of secundum atrial septal defect using Cocoon septal occluder: immediate and long-term results.

Functional Echocardiographic and Serum Biomarker Changes Following Surgical and Percutaneous Atrial Septal Defect Closure in Children.

Coronary artery embolism and acute coronary syndrome: A critical appraisal of existing data.

Cardiac remodeling after atrial septal defects device closure.

[Prevalence of congenital malformations in newborns in the Araucanía region].

A hitherto unreported combination of pulmonary stenosis, single coronary artery anomaly, and coronary sinus to left atrial communication.

Echocardiographic evaluation of total anomalous pulmonary venous connection: Comparison of obstructed and unobstructed type.

A case of 46,XY disorders of sex development with congenital heart disease caused by a GATA4 variant.

Genetic architecture in neonatal intensive care unit patients with congenital heart defects: a retrospective study from the China Neonatal Genomes Project.

TBX5 variant with the novel phenotype of mixed‑type total anomalous pulmonary venous return in Holt‑Oram Syndrome and variable intrafamilial heart defects.

Shunt in critically ill Covid-19 ARDS patients: Prevalence and impact on outcome (cross-sectional study).

The Impact of Physical Activity Restrictions on Health-Related Fitness in Children with Congenital Heart Disease.

Autosomal recessive cutis laxa type 1C with a homozygous LTBP4 splicing variant: a case report and update of literature.

PTPN11 Gene Mutations and Its Association with the Risk of Congenital Heart Disease.

Lutembacher Syndrome with Sinus Venosus-Type Interatrial Communication: An Educational Presentation.

Imaging characteristics and associations of left atrioventricular valve atresia and patent aortic root with isometric atrial appendages on multidetector CT.

Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndrome.

Congenital heart diseases trends in São Paulo State, Brazil: a national live birth data bank analysis.

Incidence, Risk Factors, and Outcomes of Atrial Arrhythmias in Adult Patients With Atrioventricular Septal Defect.

The Many Faces of the Interatrial Septum: A Diagnostic Dilemma and Considerations for Defect Closure Device Selection.

The Gore Cardioform Atrial Septal Defect Occluder: A novel solution to the management of severe hemolysis following transcatheter septal defect closure.

Long-standing hypoxaemia in complex adult congenital heart disease: anatomical and functional interplay in an uncommon presentation.

Misdiagnosis of unroofed coronary sinus syndrome as an ostium primum atrial septal defect by echocardiography: A case report.

Transient high-grade second-degree atrioventricular block secondary to transvenous atrial septal defect occlusion in a dog.

[Efficacy of fenestrated atrial septal defect occulders on pulmonary hypertension dogs].

Sinus venosus defect of the pulmonary vein-type: An easily missed diagnosis.

The presence of a large patent foramen ovale reduces acute and chronic success in atrial fibrillation ablation.

Simultaneous Percutaneous Interventional Treatment of Atrial Septal Defects and Pulmonary Valve Stenosis in Children Under the Guidance of Transoesophageal Echocardiography Alone: Preliminary Experiences.

Simultaneously Occurring Ischemic Stroke, Leg Artery Occlusion, and Pulmonary Embolism Induced by a Uterine Myoma.

Cryoballoon Atrial Fibrillation Ablation in a Patient with an Atrial Septal Defect Closure Device.

Intracardiac Repair in Late Adolescent and Adult Tetralogy of Fallot - Early and Midterm Results from a Tertiary Care Centre.

Combined transcatheter treatment of severe mitral regurgitation and secundum atrial septal defect in an inoperable patient: a case report.

Cardiac CT and Transesophageal Echocardiogram Evaluation of a Sinus Venosus-Type Atrial Septal Defect With Partial Anomalous Pulmonary Venous Return and a Persistent Left Superior Vena Cava.

From cold-blooded reptiles to embryological remnants: Persistent myocardial sinusoids.

Association of atrial septal defect and Brugada syndrome in a young woman.

No effect of patent foramen ovale on acute mountain sickness and pulmonary pressure in normobaric hypoxia.

Atrial myopathy: A primary substrate for atrial fibrillation.

Deep learning-based computer-aided heart sound analysis in children with left-to-right shunt congenital heart disease.

Familial atrial myopathy in a large multigenerational heart-hand syndrome pedigree carrying an LMNA missense variant in rod 2B domain (p.R335W).

Left atrial septal pouch in a six-year-old child: echocardiographic and magnetic resonance view.

Atrial fibrillation after closure of patent foramen ovale in the REDUCE clinical study.

First Case of Tricuspid Valve Surgery in a Neurofibromatosis Type 1 Patient.

Spatiotemporal expression of long noncoding RNA Moshe modulates heart cell lineage commitment.

Interpreting Quality Improvement When Introducing New Technology: A Collaborative Experience in ASD Device Closures.

Superior Sinus Venosus Atrial Septal Defect with Partial Anomalous Pulmonary Venous Drainage-Minimally Invasive Approach-Case Report.

Hemianomalous pulmonary venous drainage and type IIb coronary sinus septal defect - Utility of subxiphoid and right parasternal views.