Improving outcomes of biliary atresia: French national series 1986-2009.
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Pathogenesis of biliary atresia: defining biology to understand clinical phenotypesBeyond the Pediatric end-stage liver disease system: solutions for infants with biliary atresia requiring liver transplantUse of corticosteroids after hepatoportoenterostomy for bile drainage in infants with biliary atresia: the START randomized clinical trial.Alagille Syndrome Mimicking Biliary Atresia in Early Infancy.Two Rare Cases of Hepatocellular Carcinoma after Kasai Procedure for Biliary Atresia: A Recommendation for Close Follow-Up.Liver transplantation for biliary atresia: A single-center study from mainland China.Reduction of the ages at diagnosis and operation of biliary atresia in Taiwan: A 15-year population-based cohort study.Total Serum Bilirubin within 3 Months of Hepatoportoenterostomy Predicts Short-Term Outcomes in Biliary AtresiaThe Canadian Biliary Atresia Registry: Improving the care of Canadian infants with biliary atresiaCyclooxygenase-2 Inhibitor Reduces Hepatic Stiffness in Pediatric Chronic Liver Disease Patients Following Kasai Portoenterostomy.Infant Stool Color Card Screening Helps Reduce the Hospitalization Rate and Mortality of Biliary Atresia: A 14-Year Nationwide Cohort Study in Taiwan.Diagnosis of Biliary Atresia Can not be Excluded by Declining Trend of Serum Direct Bilirubin.Myofibroblastic cell activation and neovascularization predict native liver survival and development of esophageal varices in biliary atresia.Long-term results of biliary atresia in the era of liver transplantation.Clinical significance of liver histology on outcomes in biliary atresia.Impaired intention-to-treat survival after listing for liver transplantation in children with biliary atresia compared to other chronic liver diseases: 20 years' experience from the Nordic countries.Liver transplantation for biliary atresia: A nationwide investigation from 1996 to 2013 in mainland China.Bowel perforation after liver transplantation for biliary atresia: a retrospective study of care in the transition from children to adulthood.Living Related Liver Transplantation for Biliary Atresia in the Last 5 years: Experience from the First Liver Transplant Program in India.Outcome of 200 Pediatric Living Donor Liver Transplantations in India.Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome.Acoustic radiation force impulse sonography in assessing children with biliary atresia for liver transplantation.BILIARY ATRESIA: Clinical and Research Challenges for the 21st Century.Liver transplant score for prediction of biliary atresia patients' survival following Kasai procedure.Expression of intrahepatic CD3, CD4, and CD8 T cells in biliary atresia
P2860
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P2860
Improving outcomes of biliary atresia: French national series 1986-2009.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Improving outcomes of biliary atresia: French national series 1986-2009.
@en
Improving outcomes of biliary atresia: French national series 1986-2009.
@nl
type
label
Improving outcomes of biliary atresia: French national series 1986-2009.
@en
Improving outcomes of biliary atresia: French national series 1986-2009.
@nl
prefLabel
Improving outcomes of biliary atresia: French national series 1986-2009.
@en
Improving outcomes of biliary atresia: French national series 1986-2009.
@nl
P2093
P1476
Improving outcomes of biliary atresia: French national series 1986-2009.
@en
P2093
Alain Dabadie
Alain Lachaux
Bertrand Roquelaure
Chantal Buet
Christophe Chardot
Frédéric Gauthier
Frédéric Gottrand
Jean-Louis Golmard
Marie-Odile Serinet
Pierre Broué
P304
P356
10.1016/J.JHEP.2013.01.040
P577
2013-02-08T00:00:00Z