Hirschsprung disease
L Montalva, LS Cheng, R Kapur, JC Langer… - Nature Reviews …, 2023 - nature.com
Hirschsprung disease (HSCR) is a rare congenital intestinal disease that occurs in 1 in
5,000 live births. HSCR is characterized by the absence of ganglion cells in the myenteric …
5,000 live births. HSCR is characterized by the absence of ganglion cells in the myenteric …
The etiology of congenital diaphragmatic hernia: the retinoid hypothesis 20 years later
JFG Rivas, RD Clugston - Pediatric Research, 2024 - nature.com
Congenital diaphragmatic hernia (CDH) is a severe birth defect and a major cause of
neonatal respiratory distress. Impacting~ 2–3 in 10,000 births, CDH is associated with a high …
neonatal respiratory distress. Impacting~ 2–3 in 10,000 births, CDH is associated with a high …
Fetal hypoplastic lungs have multilineage inflammation that is reversed by amniotic fluid stem cell extracellular vesicle treatment
Antenatal administration of extracellular vesicles from amniotic fluid stem cells (AFSC-EVs)
reverses features of pulmonary hypoplasia in models of congenital diaphragmatic hernia …
reverses features of pulmonary hypoplasia in models of congenital diaphragmatic hernia …
A strategy to reduce the carbon footprint of clinical trials
F Adshead, RAS Salman, S Aumonier, M Collins… - The Lancet, 2021 - thelancet.com
5 Global PaedSurg Research Collaboration. Mortality from gastrointestinal congenital
anomalies at 264 hospitals in 74 low-income, middle-income, and high-income countries: a …
anomalies at 264 hospitals in 74 low-income, middle-income, and high-income countries: a …
Congenital diaphragmatic hernia
Congenital diaphragmatic hernia (CDH) is a rare birth defect characterized by incomplete
closure of the diaphragm and herniation of fetal abdominal organs into the chest that results …
closure of the diaphragm and herniation of fetal abdominal organs into the chest that results …
Establishment of a condition-specific quality-of-life questionnaire for children born with esophageal atresia aged 2–7 across 14 countries
International EA-QoL Group - Frontiers in Pediatrics, 2023 - frontiersin.org
Background Esophageal atresia (EA) is a rare congenital anomaly characterized by a
discontinuity of the esophagus. Following surgical repair, survival rates have improved …
discontinuity of the esophagus. Following surgical repair, survival rates have improved …
[HTML][HTML] Cellular origins and translational approaches to congenital diaphragmatic hernia
Abstract Congenital Diaphragmatic Hernia (CDH) is a complex developmental abnormality
characterized by abnormal lung development, a diaphragmatic defect and cardiac …
characterized by abnormal lung development, a diaphragmatic defect and cardiac …
Unraveling the genetics of congenital diaphragmatic hernia: an ongoing challenge
E Brosens, NCJ Peters, KS van Weelden… - Frontiers in …, 2022 - frontiersin.org
Congenital diaphragmatic hernia (CDH) is a congenital structural anomaly in which the
diaphragm has not developed properly. It may occur either as an isolated anomaly or with …
diaphragm has not developed properly. It may occur either as an isolated anomaly or with …
Surgical research—comic opera no more
J Bagenal, N Lee, AO Ademuyiwa, D Nepogodiev… - The Lancet, 2023 - thelancet.com
Comment www. thelancet. com Vol 402 July 8, 2023 87 profession. Women, minoritised
groups, and patients from low-income and middle-income countries remain under …
groups, and patients from low-income and middle-income countries remain under …
Identification of protein biomarkers associated with congenital diaphragmatic hernia in human amniotic fluid
Congenital diaphragmatic hernia (CDH) is a severe birth defect frequently associated with
pulmonary hypoplasia, pulmonary hypertension, and heart failure. Since amniotic fluid …
pulmonary hypoplasia, pulmonary hypertension, and heart failure. Since amniotic fluid …