Results 41 to 50 of about 613,875 (232)

Molecular signature of active fibrogenesis prevails in biliary atresia after successful portoenterostomy [PDF]

, 2017
Background. In biliary atresia mechanisms of progressive liver injury leading to need of liver transplantation after successful portoenterostomy remain unknown.
Lohi, Jouko, Mutanen, Annika, Jouko Lohi, Heikkilä, Päivi, Anna Kerola, Hanna Lampela, Päivi Heikkilä, Mikko P. Pakarinen, Kerola, Anna, Lampela, Hanna, Jalanko, Hannu, Pakarinen, Mikko P., Annika Mutanen, Hannu Jalanko   +13 more
core   +1 more source

Balloon-occluded retrograde transvenous obliteration successfully performed for a large gastric varix in combination with temporary occlusion of the splenic artery in a child

Acta Radiologica Open, 2015
We encountered a 10-year-old boy with a gastric varix that occurred after long-term treatment by Kasai’s hepatic portoenterostomy for biliary atresia for which balloon-occluded retrograde transvenous obliteration (B-RTO) was performed.
Takuji Yamagami, Rika Yoshimatsu, Kenji Kajiwara, Yoshiyuki Onitake, Eizou Hiyama, Kazuo Awai   +5 more
doaj   +1 more source

Biliary Lipid Excretion After Hepatic Portoenterostomy

Annals of Surgery, 1976
Since 1974, 16 consecutive infants with biliary atresia have been treated by hepatic portoenterostomy employing an exteriorized Roux-en-Y intestinal segment (Miluliez). Simultaneous, sequential analyses of bile pigments and lipids in serum and biliary drainage were performed.
J R, Lilly, N B, Javitt
openaire   +3 more sources

Additional file 1 of Cost-effectiveness analysis of liver transplantation in biliary atresia according to the severity of end-stage liver disease

, 2023
Additional file 1: Supplementary Table 1. Characteristics of biliary atresia children who were registered for liver transplantation according to the history of hepatic portoenterostomy (N=176)
Napapat Butsriphum (16925691), Suporn Treepongkaruna (9270421), Songpon Getsuwan (16925688), Oraluck Pattanaprateep (10988683), Chatmanee Lertudomphonwanit (16925694), Chollasak Thirapattaraphan (16925697), Boonyanurak Sihaklang (16925685), Pornthep Tanpowpong (16031243)   +7 more
core   +1 more source

Genetics of Biliary Atresia: A Work in Progress for a Disease with an Unavoidable Sequela into Liver Cirrhosis following Failure of Hepatic Portoenterostomy

Liver Cirrhosis - Debates and Current Challenges, 2019
The bile duct development may not be fully completed at birth, and this is quite a common event. Moreover, bile formation is immature, and there is a propensity for the neonate to develop cholestasis in the presence of a wide variety of insults that can ...
C. Sergi
semanticscholar   +1 more source

Clinical Characteristics and Outcome of Infants with Biliary Atresia in Bahrain

Oman Medical Journal, 2023
Objectives: Though the prevalence of biliary atresia (BA) in the Middle East is low, its role in causing life-threatening liver diseases is disproportionately high.
Hasan M. Isa, Zainab Irshad
doaj   +1 more source

Clinical Parameters and Outcomes of Biliary Atresia in Children: A Single Centre Study

Pakistan Armed Forces Medical Journal
Objective: To assess the clinical and laboratory parameters, interventions and their outcomes in children presenting with biliary atresia at a tertiary care hospital. Study Design: Prospective longitudinal study.
Raazia Nawaz, Farooq Ikram, Bilal, Saba Idrees, Ifnan Shamraiz, Samina Tabassum   +5 more
doaj   +1 more source

Improved Results with Hepatic Portoenterostomy

Annals of Surgery, 1982
As reported in 1974, the initial experience at the Oklahoma Children's Memorial Hospital with the Kasai procedure for biliary atresia was unsatisfactory. A subsequent series of 20 patients, in which 50% of the patients are alive and improved and 25% jaundice-free, is described.
E I, Smith, J A, Carson, W P, Tunell, D C, Hitch, T J, Pysher   +4 more
openaire   +3 more sources

CONTRIBUTION OF HEPATIC PORTOENTEROSTOMY IN THE TREATMENT OF BILIARY ATRESIA

, 1993
THE HEPATIC PORTOENTEROSTOMY CHANGED THE PROGNOSIS OF BILIARY ATRESIA. THE PURPOSE OF THIS STUDY IS TO ASSESS THE EFFICACY OF HEPATIC PORTOENTEROSTOMY IN TREATING 15 INFANTS WITH BILIARY ATRESIA.
Καψανάκης, Εμμανουήλ
core   +1 more source

Hepatic phenotypes of HNF1B gene mutations: a case of neonatal cholestasis requiring portoenterostomy and literature review.

World Journal of Gastroenterology, 2015
Hepatocyte nuclear factor 1-β (HNF1B) defects cause renal cysts and diabetes syndrome (RCAD), or HNF1B-maturity-onset diabetes of the young. However, the hepatic phenotype of HNF1B variants is not well studied.
R. Kotalová, P. Dusatkova, O. Cinek, L. Dušátková, T. Dědič, T. Seeman, J. Lebl, Š. Průhová   +7 more
semanticscholar   +1 more source