• A Small De Novo CNV Deletion of the Paternal Copy of <em>FOXF1</em>, Leaving lncRNA <em>FENDRR</em> Intact, Provides Insight into Their Bidirectional Promoter Region
• Alveolar capillary dysplasia with misalignment of pulmonary veins in a premature newborn: the role of lung ultrasound
• Case report: High-dose epoprostenol therapy in pediatric patients with pulmonary hypertension and developmental lung disease
• Clinical Relevance of Rapid FOXF1-Targeted Sequencing in Patients Suspected of Alveolar Capillary Dysplasia With Misalignment of Pulmonary Veins
• Demonstration of Safety in Wild Type Mice of npFOXF1, a Novel Nanoparticle-Based Gene Therapy for Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins
• Descriptive images and features of pulmonary vascular disease in a child with a FOXF1 variant
• Diagnosis and treatment of a child with alveolar capillary dysplasia with misalignment of pulmonary veins due to variant of FOXF1 gene
• Endothelial progenitor cells derived from embryonic stem cells prevent alveolar simplification in a murine model of bronchopulmonary dysplasia
• Endothelial to mesenchymal transition in neonatal hyperoxic lung injury: role of sex as a biological variable
• Endothelial-specific loss of IKKβ disrupts pulmonary endothelial angiogenesis and impairs postnatal lung growth
• Extracorporeal Membrane Oxygenation (ECMO) for suspected neonatal genetic diagnoses with cardiorespiratory failure
• Fluorinated amphiphilic Poly(β-Amino ester) nanoparticle for highly efficient and specific delivery of nucleic acids to the Lung capillary endothelium
• FOXF1 Regulates Alveolar Epithelial Morphogenesis through Transcriptional Activation of Mesenchymal WNT5A
• From 6-wk Lungs to 6 y: Increasing the Donor Pool for Pediatric Lung Transplantation
• Further refinement of the differentially methylated distant lung-specific FOXF1 enhancer in a neonate with alveolar capillary dysplasia
• Genetic analysis of an infant death due to a paternally derived FOXF1 somatic-gonadal mosaic variant
• Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins and lymphedema-distichiasis syndrome: relationship to phenotype
• Histologic features and decreased lung FOXF1 gene expression in severe bronchopulmonary dysplasia without a genetic diagnosis of alveolar capillary dysplasia
• Human lung virtual histology by multi-scale x-ray phase-contrast computed tomography
• Identification of endothelial and mesenchymal FOXF1 enhancers involved in alveolar capillary dysplasia
• Learning from cystic fibrosis: How can we start to personalise treatment of Children's Interstitial Lung Disease (chILD)?
• Lung biopsies in infants and children in critical care situation
• Megacystis in the First Trimester as an Unreported Sonographic Finding of Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins Confirmed by Whole-exome Sequencing
• Multilamellated Basement Membranes in the Capillary Network of Alveolar Capillary Dysplasia
• Neonatal Diagnosis of Alveolar Capillary Dysplasia via Rapid Genomic Sequencing: A New Gold Standard?
• New Insights into the Natural History of Bronchopulmonary Dysplasia from Proteomics and Multiplexed Immunohistochemistry
• Novel FOXF1-Stabilizing Compound TanFe Stimulates Lung Angiogenesis in Alveolar Capillary Dysplasia
• Prematurity and Hyperoxia Have Different Effects on Alveolar and Microvascular Lung Development in the Rabbit
• Prenatal Detection of a <em>FOXF1</em> Deletion in a Fetus with ACDMPV and Hydronephrosis
• Pulmonary Hypertension in Developmental Lung Diseases
• Rapid genome diagnosis of alveolar capillary dysplasia leading to treatment in a child with respiratory and cardiac failure
• Rare to "Ubiquitinous": Alveolar Capillary Dysplasia, FOXF1, and a Sly Approach to Angiogenesis
• Retrospective evaluation of neonates with fatal congenital lung malformation: A single center 15-year forensic autopsy experience
• Single Cell Multiomics Identifies Cells and Genetic Networks Underlying Alveolar Capillary Dysplasia
• Stem cell therapies for neonatal lung diseases: Are we there yet?
• Twins with alveolar capillary dysplasia with misalignment of pulmonary veins: Strategies for diagnosis and management
• Unusual presentation of alveolar capillary dysplasia with misalignment of the pulmonary veins in a child with respiratory syncytial virus pneumonia: A case report
• Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children
• When Development of the Alveolar Gas Exchange Unit Fails: Universal Single-Cell Lessons from Rare Monogenic Disorders