• <em>Truncus arteriosus communis</em>: report of three cases and review of literature
• A bicarotid trunk with associated right retroesophageal subclavian artery in a child with neurofibromatosis type 1 complicated by a left hemispheric stroke
• A case report of aorto-pulmonary window in an infant born to a diabetic mother
• A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication
• A novel NOTCH1 missense variant in two fetuses with a non-syndromic conotruncal heart defect from a single family
• Accuracy and impact of prenatal diagnosis of common arterial trunk
• Adaptive living skills, sleep problems, and mental health disorders in adults with 22q11.21 deletion syndrome
• An Anterior Second Heart Field Enhancer Regulates the Gene Regulatory Network of the Cardiac Outflow Tract
• Anomalous branching of the aortic arch in a dog
• Appropriateness of cardiovascular computed tomography and magnetic resonance imaging in patients with conotruncal defects
• Association between functional polymorphisms in the promoter of the miR-143/145 cluster and risk of conotruncal heart defects
• Biallelic alterations in PLXND1 cause common arterial trunk and other cardiac malformations in humans
• Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS
• Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach
• Clinical delineation of 18q11-q12 microdeletion: Intellectual disability, speech and behavioral disorders, and conotruncal heart defects
• Clinical value of prenatal ultrasound in diagnosis and classification of common arterial trunk
• Coexistence of dextrocardia and persistent truncus arteriosus in an adult patient
• Common Arterial Trunk in Fetal Life: Accuracy of Diagnosis and Prediction of Outcome
• Common arterial trunk in functionally univentricular hearts: a case series
• Comparison of definitive approaches for conotruncal defects following bidirectional Glenn procedure
• Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
• Completed Surgical Repair of Common Arterial Trunk Type I at 16 Years old Without Pulmonary Protection
• Congenital Aortic Valve Repair When the Options aren't Good: Truncus Arteriosus and Transposition of the Great Arteries
• Congenital heart defects in molecularly proven Kabuki syndrome patients
• Conotruncal Heart Defects: A Narrative Review of Molecular Genetics, Genomics Research and Innovation
• Contemporary Multicenter Outcomes for Truncus Arteriosus With Interrupted Aortic Arch
• Contribution of LRP1 in Human Congenital Heart Disease Correlates with Its Roles in the Outflow Tract and Atrioventricular Cushion Development
• Copy number variations in individuals with conotruncal heart defects reveal some shared developmental pathways irrespective of 22q11.2 deletion status
• Cord blood cardiovascular biomarkers in tetralogy of fallot and D-transposition of great arteries
• Diagnosis of major heart defects by routine first-trimester ultrasound examination: association with increased nuchal translucency, tricuspid regurgitation and abnormal flow in ductus venosus
• Diagnostic Value of Chromosomal Microarray Analysis for Fetal Congenital Heart Defects with Different Cardiac Phenotypes and Extracardiac Abnormalities
• Discordant atrioventricular connections with truncus arteriosus
• Early Bidirectional Glenn Procedure as Initial Surgical Palliation for Functionally Univentricular Heart with Common Arterial Trunk
• Echocardiography: conotruncal anomaly: a case of common arterial trunk with intact ventricular septum and hypoplastic left heart complex with unbalanced pulmonary stenoses
• Ectopia cordis: prenatal diagnosis, perinatal outcomes, and postnatal follow-up of an international multicenter cohort case series
• Epigenetics of conotruncal congenital heart disease: Protocol for a systematic review and meta-analysis
• Evaluating High-Confidence Genes in Conotruncal Cardiac Defects by Gene Burden Analyses
• Ex utero intrapartum treatment-to-extracorporeal membrane oxygenation followed by cardiac operation for truncus arteriosus communis
• Extrahepatic approach for taping the common trunk of the middle and left hepatic veins or the left hepatic vein alone in laparoscopic hepatectomy (with videos)
• Fetal Echocardiographic Variables Associated with Pre-Surgical Mortality in Truncus Arteriosus: A Pilot Study
• Flow visualization of a unique case of persistent truncus arteriosus with prolonged survival
• Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects
• Gene-based genome-wide association studies and meta-analyses of conotruncal heart defects
• Gene-by-gene interactions associated with the risk of conotruncal heart defects
• Genetic variation in folate metabolism is associated with the risk of conotruncal heart defects in a Chinese population
• HAND transcription factors cooperatively specify the aorta and pulmonary trunk
• How I do it: endoscopic microvascular decompression for hemifacial spasm associated with anterior inferior cerebellar artery-posterior inferior cerebellar artery common trunk
• Identification of FOXH1 mutations in patients with sporadic conotruncal heart defect
• Identification of TBX2 and TBX3 variants in patients with conotruncal heart defects by target sequencing
• Identification of ZFPM2 mutations in sporadic conotruncal heart defect patients
• In Silico Analyses Reveal the Relationship Between SIX1/EYA1 Mutations and Conotruncal Heart Defects
• Injury of the common hepatic artery during esophagectomy caused by an anatomical variation branching from a common trunk with the left gastric artery: A case report
• Laparoscopic radical resection for rectal cancer in a patient with uncorrected truncus arteriosus type IV: A case report
• Left Atrial Ligation in the Avian Embryo as a Model for Altered Hemodynamic Loading During Early Vascular Development
• Letter to the editor regarding: "A rare case of CHD: anomalous origin of coronary artery from innominate artery with coronary fistula and truncus arteriosus"
• Lingular division of the left lung: Only superior and inferior bronchi?
• LRP2 controls sonic hedgehog-dependent differentiation of cardiac progenitor cells during outflow tract formation
• Maternal exposure to ambient ozone and fetal conotruncal heart defects in China: A multicenter cohort study
• National population-based estimates for major birth defects, 2016-2020
• Natural History of Truncal Root Dilatation and Truncal Valve Regurgitation in Truncus Arteriosus
• Neighborhood location and nutritional resources as a risk factor for congenital heart disease in the fetus
• Neuroendocrine tumors and conotruncal cardiac defects
• New drug-like small molecule antagonizes phosphatidylinositol (3,4,5)-trisphosphate (PIP3) in patients with conotruncal heart defects
• Non-Conduit Repair of Truncus Arteriosus
• Novel mutations of the SRF gene in Chinese sporadic conotruncal heart defect patients
• Novel pathogenic GATA6 variant associated with congenital heart disease, diabetes mellitus and necrotizing enterocolitis
• Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease Phenotypes
• Outcome of truncus arteriosus repair: 20 years of single-center experience comparing early versus late surgical repair
• Outcomes in Primary Repair of Truncus Arteriosus with Significant Truncal Valve Insufficiency: A Systematic Review and Meta-analysis
• Outcomes of truncal valve replacement in neonates and infants: a meta-analysis
• Over-expression of Fgf8 in cardiac neural crest cells leads to persistent truncus arteriosus
• Oxidative balance scores and neural crest cell-related congenital anomalies
• PHACES-like syndrome with TMEM260 compound heterozygous variants
• Pharyngeal epithelial deletion of Tbx1 causes caudal pharyngeal arch defect but not cardiac conotruncal anomaly
• Platelet parameters in children with chromosome 22q11 deletion and conotruncal heart defects
• Polymorphisms in gene <em>UGT1A1</em> modify the association of prenatal exposure to polycyclic aromatic hydrocarbons with congenital heart diseases risk
• Prenatal diagnosis, associated findings and postnatal outcome of fetuses with truncus arteriosus communis (TAC)
• Prenatal exome sequencing in fetuses with congenital heart defects
• Prenatally detected aortic arch anomalies and their consequences after birth
• Pulmonary hypoplasia in fetuses with congenital conotruncal defects
• Repair of common arterial trunk: palliation and delayed correction as a viable alternative strategy in selected patients
• Repair of truncus arteriosus and atrioventricular septal defect: A value of virtual reality
• Right Ventricular Outflow Tract Reconstruction in Truncus Arteriosus: A 30-Year Two-Center Comparison between Homografts and Bovine Jugular Vein
• Routine Contrasted Chest CT Accurately Identifies Anatomic Variations of the Proximal Subscapular System
• Safety of Continuing Anticoagulation Prior to Cardiac Catheterization in Pediatric Patients: A Los Angeles Center Experience
• SOX7 suppresses endothelial-to-mesenchymal transitions by enhancing VE-cadherin expression during outflow tract development
• Strategies for Complex Reoperative Aortic Arch Reconstruction in Patients With Congenital Heart Disease
• Surgical Repair of a Rare Variant of Common Arterial Trunk, With Considerations of its Significance for Morphogenesis
• Survival After Single-Stage Repair of Truncus Arteriosus and Associated Defects
• Targeted sequencing identifies novel GATA6 variants in a large cohort of patients with conotruncal heart defects
• The evolving genetic etiology of conotruncal anomalies
• The prevalence of abnormal spirometry in children with CHD
• Tracheobronchial Release for Left Bronchus Compression After Aortic Arch Repair
• Transpositions of the great arteries versus aortic dextropositions. A review of some embryogenetic and morphological aspects
• Tricuspid atresia and common arterial trunk: a rare form of CHD
• Truncus arteriosus communis associated with interrupted aortic arch - Type B and right aberrant subclavian artery: A rare entity
• Truncus arteriosus with absent semilunar valve: Prenatal diagnosis and morphology
• Use of 3D volume-rendered CT imaging in analysing the anatomy of an unusual type of common arterial trunk
• Variants in FOXC1 and FOXC2 identified in patients with conotruncal heart defects
• What is the impact of a novel MED12 variant on syndromic conotruncal heart defects? Analysis of case report on two male sibs