Meconium Peritonitis, Intestinal Atresia Combined With Biliary Atresia: A Case Report. [PDF]
Front Pediatr, 2022 Han Y +5 more
europepmc +1 more source
Experience with Tapering Enteroplasty in Intestinal Atresia [PDF]
, 2007 Jae Hee Chung +2 more
openalex +1 more source
Evaluation of postoperative feeding strategies in children with intestinal atresia: A single-center retrospective study. [PDF]
Front Pediatr, 2022 Wang J, Xu H, Wang J, Xiao D.
europepmc +1 more source
A One‐Dimensional (1D) Computational Fluid Dynamics Study of Fontan‐Associated Liver Disease (FALD)
International Journal for Numerical Methods in Biomedical Engineering, Volume 42, Issue 1, January 2026.Fontan‐associated liver disease (FALD) is a disorder arising from congestion in the liver. This disease is prominent in patients with hypoplastic left heart syndrome (HLHS). Through perfusion analysis, we find that as FALD progresses, there are increased pressures and decreased flow to certain regions of liver tissue.
Yaqi Li +4 more
wiley +1 more source
The multivariate cox regression model for complete enteral nutrition after primary anastomosis in neonates with intestinal atresia. [PDF]
Front Pediatr, 2022 Chen Y +7 more
europepmc +1 more source
A Rational Approach to Pharmacotherapy in Pregnancy
The Journal of Clinical Pharmacology, Volume 66, Issue 1, January 2026.Abstract Most pregnant individuals are exposed to at least one medication, whether prescription or over the counter, during pregnancy. Despite the ubiquity of medication use in pregnancy, there remains no standardized framework to guide clinicians in selecting the most appropriate pharmacotherapy that balances maternal needs with fetal safety. This gap
Gregory W. Kirschen +2 more
wiley +1 more source
Rare case report of anorectal malformation and intestinal atresia. [PDF]
Int J Surg Case Rep, 2021 Gunderson EJ +5 more
europepmc +1 more source
Imperforate Anus with Jejunal Atresia Complicated by Intestinal Volvulus: A Case Report
, 2016 Rachel Hae‐Soo Joung +3 more
openalex +1 more source
Holocarboxylase Synthetase Deficiency: A Second Case Report With Neonatal Cholestatic Liver Disease
JIMD Reports, Volume 67, Issue 1, January 2026.ABSTRACT Holocarboxylase synthetase deficiency is an autosomal recessive inborn error of metabolism characterised by life‐threatening metabolic acidosis, ketoacidosis and hyperammonaemia through reduced biotin‐dependent carboxylase activity. We report the presentation of a Polynesian neonate with severe metabolic acidosis secondary to holocarboxylase ...
Sophie Manoy +9 more
wiley +1 more source