Use of corticosteroids after hepatoportoenterostomy for bile drainage in infants with biliary atresia: the START randomized clinical trial.
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Recent Trends in the Diagnosis and Management of Biliary Atresia in Developing CountriesZebrafish: an important tool for liver disease researchPathogenesis of biliary atresia: defining biology to understand clinical phenotypesBeyond the Pediatric end-stage liver disease system: solutions for infants with biliary atresia requiring liver transplantTotal serum bilirubin predicts fat-soluble vitamin deficiency better than serum bile acids in infants with biliary atresia.Recent advances in the pathogenesis and management of biliary atresiaAdjuvant steroid treatment following Kasai portoenterostomy and clinical outcomes of biliary atresia patients: an updated meta-analysis.Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis.Targeting extracellular cyclophilins ameliorates disease progression in experimental biliary atresia.Steroids after the Kasai procedure for biliary atresia: the effect of age at Kasai portoenterostomy.Total Serum Bilirubin within 3 Months of Hepatoportoenterostomy Predicts Short-Term Outcomes in Biliary AtresiaBiliary atresia: Where do we stand now?Glucocorticoids Have Opposing Effects on Liver Fibrosis in Hepatic Stellate and Immune CellsClinical significance of liver histology on outcomes in biliary atresia.Key Histopathologic Features of Liver Biopsies That Distinguish Biliary Atresia From Other Causes of Infantile Cholestasis and Their Correlation With Outcome: A Multicenter Study.Hepatic Hilar Lymph Node Reactivity at Kasai Portoenterostomy for Biliary Atresia.Adjuvant therapy in biliary atresia: hopelessly optimistic or potential for change?The Sea Lamprey as an Etiological Model for Biliary Atresia.Laparoscopic portoenterostomy for biliary atresia: single-center experience and review of literatures.Biliary atresia: unity in diversity.Update on investigations pertaining to the pathogenesis of biliary atresia.BILIARY ATRESIA: Clinical and Research Challenges for the 21st Century.Neurodevelopmental Outcome of Young Children with Biliary Atresia and Native Liver: Results from the ChiLDReN Study.Long-term native liver survival in infants with biliary atresia and use of a stool color card: Case-control study.
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P2860
Use of corticosteroids after hepatoportoenterostomy for bile drainage in infants with biliary atresia: the START randomized clinical trial.
description
2014 nî lūn-bûn
@nan
2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Use of corticosteroids after h ...... ART randomized clinical trial.
@ast
Use of corticosteroids after h ...... ART randomized clinical trial.
@en
Use of corticosteroids after h ...... ART randomized clinical trial.
@nl
type
label
Use of corticosteroids after h ...... ART randomized clinical trial.
@ast
Use of corticosteroids after h ...... ART randomized clinical trial.
@en
Use of corticosteroids after h ...... ART randomized clinical trial.
@nl
prefLabel
Use of corticosteroids after h ...... ART randomized clinical trial.
@ast
Use of corticosteroids after h ...... ART randomized clinical trial.
@en
Use of corticosteroids after h ...... ART randomized clinical trial.
@nl
P2093
P2860
P356
P1476
Use of corticosteroids after h ...... ART randomized clinical trial.
@en
P2093
Averell H Sherker
Barbara Haber
Benjamin L Shneider
Cathie Spino
Childhood Liver Disease Research and Education Network (ChiLDREN)
Frederick J Suchy
Jeffrey Moore
Jessi Erlichman
John C Magee
Jorge A Bezerra
P2860
P304
P356
10.1001/JAMA.2014.2623
P407
P577
2014-05-01T00:00:00Z