Results 91 to 100 of about 226,924 (326)

Biliary atresia: Potential for a new decade.

open access: yesSeminars in Pediatric Surgery, 2020
Biliary atresia is characterised as an obliterative cholangiopathy of both extra-and intra-hepatic bile ducts. There is marked aetiological heterogeneity with a number of different variants, some syndromic and others perhaps virally-mediated.
F. Scottoni, M. Davenport
semanticscholar   +1 more source

Rotavirus Reassortant–Induced Murine Model of Liver Fibrosis Parallels Human Biliary Atresia

open access: yesHepatology, 2020
Biliary atresia (BA) is a devastating neonatal cholangiopathy that progresses to fibrosis and end‐stage liver disease by 2 years of age. Portoenterostomy may reestablish biliary drainage, but, despite drainage, virtually all afflicted patients develop ...
S. Mohanty   +14 more
semanticscholar   +1 more source

The Surgery of Biliary Atresia

open access: yesAnnals of Surgery, 1989
One hundred thirty-one consecutive infants with biliary atresia were operated on during the 15-year period between 1973 and 1988. Six patients did not have biliary reconstruction because of advanced cirrhosis or transplant preference. The other 125 infants had excision of all nonpatent extrahepatic bile ducts; biliary drainage was provided by a ...
J R, Lilly   +7 more
openaire   +3 more sources

Human Cyclophilins—An Emerging Class of Drug Targets

open access: yesMedicinal Research Reviews, EarlyView.
ABSTRACT Cyclophilins are a family of enzymes with peptidyl‐prolyl isomerase activity found in all cells of all organisms. To date, 17 cyclophilin isoforms have been identified in the human body, participating in diverse biological processes. Consequently, cyclophilins have emerged as promising targets for drug development to address a wide array of ...
Katarina Jurkova   +3 more
wiley   +1 more source

Weaning of immunosuppression in long - Term liver transplant recipients [PDF]

open access: yes, 1995
Seventy-two long-surviving liver transplant recipients were evaluated prospectively, including a baseline allograft biopsy for weaning off of immunosuppression.
Abu-Elmagd, K   +11 more
core   +1 more source

Rotavirus Infection and Cytopathogenesis in Human Biliary Organoids Potentially Recapitulate Biliary Atresia Development

open access: yesmBio, 2020
There is substantial evidence indicating the possible involvement of rotavirus in biliary atresia (BA) development, at least in a subset of patients, but concrete proof remains lacking.
Sunrui Chen   +8 more
semanticscholar   +1 more source

Application of machine learning in constructing a diagnostic model for neonatal biliary atresia

open access: yesPediatric Investigation, EarlyView.
This study included 85 neonates who visited the hospital due to pathological jaundice. Using the basic clinical characteristics and serological examination data of the neonatal period, we developed six machine‐learning (ML) models. Extreme gradient boosting has the maximum potential to diagnose biliary atresia in the neonatal period.
Dingding Wang   +11 more
wiley   +1 more source

Clinical practice guidelines for biliary atresia in Japan: A secondary publication of the abbreviated version translated into English

open access: yesJournal of hepato-biliary-pancreatic sciences, 2020
The purpose of this study was to prepare clinical practice guidelines for biliary atresia according to the Medical Information Network Distribution Service (MINDS) Handbook for Clinical Practice Guideline Development 2014.
Hisami Ando   +6 more
semanticscholar   +1 more source

Physiologically‐Based Pharmacokinetic Modeling to Support Pediatric Clinical Development: An IQ Working Group Perspective on the Current Status and Challenges

open access: yesCPT: Pharmacometrics &Systems Pharmacology, EarlyView.
ABSTRACT Pediatric extrapolation strategies issued by health authorities have streamlined pediatric drug development and reduced the unnecessary burden of conducting pediatric clinical studies. In line with these strategies, physiologically based pharmacokinetic (PBPK) models have been utilized extensively for initial dosing regimen and sampling ...
James W. T. Yates   +26 more
wiley   +1 more source

Long Noncoding RNA H19 Contributes to Cholangiocyte Proliferation and Cholestatic Liver Fibrosis in Biliary Atresia

open access: yesHepatology, 2019
Biliary atresia (BA) is a neonatal liver disease featuring cholestasis and severe liver fibrosis (LF). Despite advances in the development of surgical treatment, lacking an early diagnostic marker and intervention of LF invariably leads to death from end‐
Yongtao Xiao   +7 more
semanticscholar   +1 more source

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