Results 101 to 110 of about 21,958 (289)
Biliary atresia associated with choledochal cyst
African Journal of Paediatric Surgery, 2009 Choledochal cyst and biliary atresia are rare but important causes of neonatal jaundice. Both present with jaundice and acholic stool in neonatal period. Treatment and prognosis of both entities are very different.
Obaidah Abu +3 more
doaj
Association of biliary atresia with jejuno-ileal atresia: Case report
Journal of Pediatric Surgery Case Reports, 2023 Background: Jejuno‐ileal atresia (JIA) is a congenital anomaly characterized clinically by bilious vomiting and abdominal distension. The incidence of JIA is approximately between 1 in 5000 live births in different parts of the world.
Amru Abulkhair +7 more
doaj
The R Package JMbayes for Fitting Joint Models for Longitudinal and Time-to-Event Data using MCMC [PDF]
arXiv, 2014 Joint models for longitudinal and time-to-event data constitute an attractive modeling framework that has received a lot of interest in the recent years. This paper presents the capabilities of the R package JMbayes for fitting these models under a Bayesian approach using Markon chain Monte Carlo algorithms. JMbayes can fit a wide range of joint models,
arxiv
Contribution of resident stem cells to liver and biliary tree regeneration in human diseases [PDF]
, 2018 Two distinct stem/progenitor cell populations of biliary origin have been identified in the adult liver and biliary tree. Hepatic Stem/progenitor Cells (HpSCs) are bipotent progenitor cells located within the canals of Hering and can be differentiated ...
Alvaro, Domenico +7 more
core +1 more source
COG6‐related prenatal phenotype (CDG2L): Clinico‐pathological report and review of the literature
Molecular Genetics &Genomic Medicine, Volume 13, Issue 4, April 2025.Abstract Background CDG2L (MIM#614576) is an autosomal recessive multisystemic disorder due to variants in COG6 gene. Postnatal phenotypes are now well described, while prenatal presentations remain poorly investigated. Only 8 of the 28 published patients have had prenatal ultrasound anomalies reported and no one post‐mortem investigation.
Sarah Guterman +17 more
wiley +1 more source
Gastro Hep Advances, 2023 Background and Aims: Biliary atresia is a rare and devastating bile duct disease that occurs during the neonatal period. Timely identification and prompt surgical intervention is critical for improving the outcome.
Ho Jung Choi +15 more
doaj
L0 regularisation for the estimation of piecewise constant hazard rates in survival analysis [PDF]
arXiv, 2016 In a survival analysis context we suggest a new method to estimate the piecewise constant hazard rate model. The method provides an automatic procedure to find the number and location of cut points and to estimate the hazard on each cut interval. Estimation is performed through a penalized likelihood using an adaptive ridge procedure.
arxiv
A rare case of Biliary Atresia with Biliary Ascites on a (Hepatobiliary Iminodiacetic Acid) HIDA scan [PDF]
Biliary atresia is one of the most challenging conditions in pediatric surgery even when it is the only finding. Here we present a rare case of biliary atresia complicated with biliary ascites due to ductal perforation identified on a hepatobiliary ...
Gitau, Samuel +2 more
core +2 more sources
Nutrition in Clinical Practice, Volume 40, Issue 2, Page 496-507, April 2025.Abstract Gastroschisis is a leading cause of pediatric intestinal failure. Feeding guidelines may lead to improved patient outcomes including decreased time to reach full feeds, a reduction in the duration of parenteral nutrition, and reduced length of stay.
Andrea Adler +2 more
wiley +1 more source
Scientific ReportsBile acids have received increasing attention as a marker of the long-term prognosis and a potential therapeutic target in patients with biliary atresia, which is a progressive disease of the hepatobiliary system. A detailed analysis of serum and urinary
Masahiro Takeda +9 more
doaj +1 more source