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Liver Transplantation

Free Subscription Articles published in Pediatr Surg Int Retrieve available abstracts of 15 articles: HTML format

Single Articles

November 2025
1. SUTTHATARN P, Taesombat W, Kruephate M, Sirichindakul P, et al
   Outcomes of major liver resection for children with hepatoblastoma weighing less than 10 kg: avoiding liver transplantation with extended or extreme resection.
   Pediatr Surg Int. 2025;42:29.
   PubMed    
   
   
   
2. OCHI T, Takeda M, Asahara T, Kurita A, et al
   Postoperative gut dysbiosis in biliary atresia patients treated by portoenterostomy or liver transplantation.
   Pediatr Surg Int. 2025;42:9.
   PubMed     Abstract available
   
   
   September 2025
3. TIAN Y, Lian H, Ye M, Shao Y, et al
   Evaluating the role of Kasai portoenterostomy in biliary atresia older than 90 days.
   Pediatr Surg Int. 2025;41:285.
   PubMed     Abstract available
   
   
   July 2025
4. OOI LL, Oi JAW, Ng KWS, Loh PS, et al
   Initiating a paediatric living donor liver transplant program in a resource-challenged environment: outcomes and lessons learned.
   Pediatr Surg Int. 2025;41:213.
   PubMed     Abstract available
   
   
   December 2024
5. SINGHAI P, Solanki S, Kanojia RP, Peters NJ, et al
   Impact of socioeconomic and geographical factors on clinical care of biliary atresia patients: a cross-sectional study.
   Pediatr Surg Int. 2024;41:53.
   PubMed     Abstract available
   
   
   August 2024
6. TORIIGAHARA Y, Matsuura T, Takahashi Y, Uchida Y, et al
   A retrospective study investigating the risk of graft loss in living donor liver transplant cases where size mismatching is predicted from graft-to-recipient weight ratio.
   Pediatr Surg Int. 2024;40:229.
   PubMed     Abstract available
   
   
   
7. TAKAHASHI Y, Matsuura T, Maeda S, Uchida Y, et al
   Factors predicting the need for liver transplantation in biliary atresia patients after 18 years of age.
   Pediatr Surg Int. 2024;40:218.
   PubMed     Abstract available
   
   
   July 2024
8. GOHDA Y, Uchida H, Sumida W, Shirota C, et al
   Bile lakes in patients with biliary atresia who presented with jaundice-free native liver survival indicating the risk of subsequent liver transplantation due to various factors.
   Pediatr Surg Int. 2024;40:197.
   PubMed     Abstract available
   
   
   
9. HARUMATSU T, Muraji T, Masuya R, Tsuruno Y, et al
   Inflammation patterns in early post-operative cholangitis predict long-term outcomes in biliary atresia: a potential role of non-suppurative cholangitis.
   Pediatr Surg Int. 2024;40:190.
   PubMed     Abstract available
   
   
   May 2024
10. KARAYAZILI M, Celtik U, Ataseven E, Nart D, et al
    Evaluation of surgical strategies and long-term outcomes in pediatric hepatocellular carcinoma.
    Pediatr Surg Int. 2024;40:144.
    PubMed     Abstract available
    
    
    April 2024
11. QIAN Y, Zhang W, Wang W, Li Z, et al
    Risk factors for post-operative portal vein stenosis in pediatric liver transplantation: a single center case-control study.
    Pediatr Surg Int. 2024;40:113.
    PubMed     Abstract available
    
    
    November 2023
12. TORIIGAHARA Y, Matsuura T, Yanagi Y, Yoshimaru K, et al
    The advantages of duct-to-duct biliary reconstruction in pediatric living donor liver transplantation.
    Pediatr Surg Int. 2023;39:286.
    PubMed     Abstract available
    
    
    September 2023
13. KAWAGUCHI Y, Terui K, Takenouchi A, Komatsu S, et al
    Outcomes of adult native liver survivors with biliary atresia: the current situation in Japan.
    Pediatr Surg Int. 2023;39:263.
    PubMed     Abstract available
    
    
    August 2023
14. TANAKA H
    Advances in pediatric liver transplantation from the pediatric surgeon's perspective.
    Pediatr Surg Int. 2023;39:253.
    PubMed     Abstract available
    
    
    February 2023
15. WICKRAMASEKARA N, Ignatius J, Lamahewage A
    Prognostic factors and outcomes of Kasai portoenterostomy (KPE): nine-year experience from a lower-middle income country.
    Pediatr Surg Int. 2023;39:142.
    PubMed     Abstract available
    
    

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