• 2024 CSANZ Position Statement on Indications, Assessment and Monitoring of Structural and Valvular Heart Disease With Transthoracic Echocardiography in Adults
• 64-Slice ECG-gated computed tomographic angiography for assessment of coronary arteries in brachycephalic dogs with pulmonary stenosis
• A 20-year follow-up of successful surgical management for a complex case of pentalogy of fallot and dextrocardia with systemic and pulmonary venous anomalies: A rare case report
• A 25-Year-Old With an Incidentally Detected Ascending Thoracic Aortic Aneurysm and Bicuspid Aortic Valve
• A rare case of diagnosed absent aortic valve and severely hypoplastic pulmonary valve with double outlet right ventricle: A case report
• Abnormal Right Ventricular-Pulmonary Arterial Coupling in Patients With Coarctation of Aorta Presenting With Aortic Stenosis
• Adaptive Growth of the Ductus Arteriosus and Aortic Isthmus in Various Ductus-Dependent Complex Congenital Heart Diseases
• Anatomical and physiological diagnostic discrepancies in fetuses with single-ventricle congenital heart disease in a contemporary cohort
• Anomalous arising of left coronary artery from the pulmonary artery (ALCAPA)
• Aortic Valve Replacement
• Aortic Valvular Atresia
• Assess the Outcomes of Transcatheter Aortic Valve Replacement in Bicuspid Valve with Mixed Disease versus Predominant Aortic Stenosis
• Biallelic variants in NUDCD2 associated with a multiple malformation syndrome with cholestasis and renal failure
• Cardiac Mechanics and Valvular and Vascular Abnormalities in Hypereosinophilic Syndrome
• Cardiac screening in pediatric patients with neurofibromatosis type 1: similarities with Noonan syndrome?
• Cardiac Surgery
• Catheter Management of Mitral Regurgitation
• Clinical and echocardiographic findings in patients with COVID-19 across different severity levels
• Clinical Application of Exercise Stress Echocardiography in an Outpatient Pediatric Population
• Clinical presentation and surgical outcomes in patients with Shone's complex: a systematic review
• Clinical Presentation and Therapy of d-Transposition of the Great Arteries
• Clinical Presentation and Therapy of Hypoplastic Left Heart Syndrome
• Clinical Presentation and Therapy of Tetralogy of Fallot and Double-Outlet Right Ventricle
• Clinical Presentation and Therapy of Truncus Arteriosus
• Congenital Blood Cyst of a Child: A case report and review of literature
• Congenital Lobar Emphysema
• Congenital lower urinary tract obstruction with spontaneous fetal bladder rupture due to posterior urethral valves: a case report
• Congenitally Corrected Transposition of the Great Arteries: Fetal Diagnosis, Associations, and Postnatal Outcome: A Fetal Heart Society Research Collaborative Study
• Current status of transcatheter intervention for complex right ventricular outflow tract abnormalities
• Diagnosis and surgical treatment of high-risk anomalous aortic origin of coronary artery
• Dichorionic Diamniotic Twin Pairs with Complex Congenital Heart Disease
• Diffuse interstitial lung disease in a male fetus with periventricular nodular heterotopia and filamin A mosaic variant
• Ebstein Anomaly and Malformation
• ECG left ventricular hypertrophy in aortic stenosis: Relationship with cardiac structure, invasive hemodynamics, and long-term mortality
• Echocardiographic Parameters and Complication Profiles Among Adult Patients with Rheumatic Heart Disease at Jimma Medical Center
• ERS/ESTS/ESTRO/ESR/ESTI/EFOMP statement on management of incidental findings from low dose CT screening for lung cancer
• ERS/ESTS/ESTRO/ESR/ESTI/EFOMP statement on management of incidental findings from low dose CT screening for lung cancer
• Frequency of Cardiac Valvulopathies in Patients With Marfan Syndrome: A Systematic Review and Meta-Analysis
• Half-turned truncal switch operation for dextro-transposition of the great arteries with ventricular septal defect and left ventricular outflow tract obstruction and an abnormal coronary pattern
• Heart transplantation using a donor heart with repaired tetralogy of Fallot: a case report
• Huge congenital right ventricular diverticulum in tetralogy of Fallot with pulmonary atresia: A double trouble
• Human Genetics of Semilunar Valve and Aortic Arch Anomalies
• Hydrops fetalis caused by a complex congenital heart defect with concurrent hypoplasia of pulmonary blood vessels and lungs visualized by micro-CT in a French Bulldog
• Impaired Distensibility of the Proximal Aorta in Fetuses With Tetralogy of Fallot
• Incidence of quadricuspid pulmonary valves at postmortem examination
• Incidence, Predictors, and Outcomes of Paravalvular Regurgitation After TAVR in Sievers Type 1 Bicuspid Aortic Valves
• Kartagener's Syndrome Complicated by Bronchiectasis with Tricuspid and Mitral Valve Regurgitation: A Case Report
• Large cameral coronary artery fistula in a 5 months old infant with unusual presentation and fatal outcome: -case report
• Longitudinal ECG changes in tetralogy of Fallot and association with surgical repair
• Looking at a baby's heart through the lens of the mother's blood
• Lower Urinary Tract Obstruction in Newborns
• MEMS Technology in Cardiology: Advancements and Applications in Heart Failure Management Focusing on the CardioMEMS Device
• Molecular and phenotypic spectrum of cardio-facio-cutaneous syndrome in Chinese patients
• Molecular Pathways and Animal Models of Semilunar Valve and Aortic Arch Anomalies
• Mycoplasma spp. pneumonia and subsequent pulmonary hypertension in a domestic ferret (Mustela putorius furo)
• Outcomes After Hybrid Palliation for Infants With Critical Left Heart Obstruction
• Paradox of disproportionate atrial functional mitral regurgitation and survival after transcatheter edge-to-edge repair
• Partial Heart Transplant in a Neonate With Irreparable Truncal Valve Dysfunction
• Pattern of cardiovascular diseases at a teaching hospital in Addis Ababa, Ethiopia: An echocardiographic study of 1500 patients
• Perinatal Diagnosis and Management of a Case with Interrupted Aortic Arch, Pulmonary Valve Dysplasia and 22q11.2 Deletion: A Case Report
• Perinatal outcomes following early prenatal diagnosis: insights from a single-center experience with Ebstein anomaly and tricuspid valve dysplasia
• Perioperative Right Ventricular Dysfunction and Abnormalities of the Tricuspid Valve Apparatus in Patients Undergoing Cardiac Surgery
• Pharmacologic Stress Testing
• Posterior mitral leaflet cleft in nonobstructive hypertrophic cardiomiopathy
• Primary Severe Pulmonary and Tricuspid Valve Regurgitation in an Adult Patient
• Prognostic Implication of Pulmonary Arterial Pressure in Surgical Repair of Predominantly Congenital Mitral Valve Regurgitation-Based Intracardiac Abnormalities
• Pulmonary artery banding and arch repair versus Norwood for unbalanced atrioventricular canal defect
• Pulmonary valve stenosis in a recipient twin in twin-to-twin transfusion syndrome with successful balloon valvuloplasty after birth: a case report
• Quadricuspid Aortic Valve: Interesting Images
• Quadricuspid pulmonary valve: A rare cause of pulmonary artery aneurysm
• Quantifying aortic valve regurgitation in patients with congenital aortic valve disease by 2D and 4D flow magnetic resonance analysis
• Redo mitral valve replacement in an adult with severe pulmonary hypertension resulting from structural valve deterioration and left ventricular outflow tract obstruction and a history of atrioventricular septal defect repair: a case report
• Régurgitation mitrale sévère due à la sarcoïdose cardiaque : une présentation clinique inhabituelle ; une étude de cas et des recherches antérieures
• Rehabilitation in a Pediatric Patient Who Underwent Correction Surgery for Tetralogy of Fallot: A Case Report
• Relationship between diagnosis of conus arteriosus malformation and genetic diagnosis results in fetal cardiac axis abnormalities by echocardiography during middle pregnancy
• Repaired Tetralogy of Fallot: Have We Understood the Right Timing of PVR?
• Revealing the true nature of a parachute mitral valve during an ultra-trail race
• Right Ventricular Hypertrophy
• Secondary tricuspid regurgitation: incidence, types, and outcomes in atrial fibrillation vs. sinus rhythm
• Severe Myxomatous Mitral Regurgitation With Normal Left Ventricular Function in a Woman With an Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery
• Sinus rhythm QRS morphology reflects right ventricular activation and anatomical ventricular tachycardia isthmus conduction in repaired tetralogy of Fallot
• Sunspot activity and birth defects among Texas births (1999-2016)
• Systematic review of cardiovascular neurocristopathy-contemporary insights and future perspectives
• Tetralogy of Fallot with an Anomalous Course of the Brachiocephalic Vein
• The Connection Between Anatomical Substrate and Clinical Severity in Fetal Ebstein Anomaly
• The First Korean Case with Cardiac, Facial, and Digital Anomalies with Developmental Delay Caused by De Novo <em>TRAF7</em> p.Arg655Gln Variant
• The infected right ventricular outflow tract in children and adults with congenital heart disease
• The Natural History of Atrial Functional Mitral Regurgitation
• Three-Dimensional Echocardiography: A Promising Tool for the Diagnosis of Quadricuspid Pulmonary Valve and Pulmonary Artery Aneurysm
• Traditional and Advanced Echocardiographic Evaluation in Chronic Obstructive Pulmonary Disease: The Forgotten Relation
• Traditional and Advanced Echocardiographic Evaluation in Chronic Obstructive Pulmonary Disease: The Forgotten Relationship
• Transcatheter closure of atrial septal defect in the elderly: a systematic review and meta-analysis
• Tricuspid Atresia
• Tricuspid Atresia with Absent Pulmonary Valve with Nearly Discontinuous Branch Pulmonary Arteries
• Truncus Arteriosus
• Ultrasound parameters of arteries and heart in normal fetuses
• Unmet Clinical Needs for Transcatheter Pulmonary Valves
• Unusual Left Superior Vena Cava, Connected to the Left Atrium via the Left Superior Pulmonary Vein
• Unveiling Lung Adenocarcinoma: Non-bacterial Thrombotic Endocarditis as the Debut Sign
• Wnt Signaling Inhibition Prevents Postnatal Inflammation and Disease Progression in Mouse Congenital Myxomatous Valve Disease