Biliary atresia and the Kasai portoenterostomy: Never say never?

Liver Transplantation

Volumn 7, Issue 9, 2001, Pages 831-832

  Ishitani, Michael B ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN;

AGE; ARTICLE; BILE DUCT ATRESIA; CHILD CARE; CLINICAL ARTICLE; CLINICAL FEATURE; COHORT ANALYSIS; CONTROLLED STUDY; DEMOGRAPHY; FEMALE; FOLLOW UP; HUMAN; INFANT; LIVER TRANSPLANTATION; MALE; MEDICAL ASSESSMENT; MEDICAL RECORD; NEGRO; PORTOENTEROSTOMY; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SURGICAL TECHNIQUE; SURVIVAL RATE; TIME; TREATMENT CONTRAINDICATION; TREATMENT OUTCOME;

EID: 0034849327     PISSN: 15276465     EISSN: None     Source Type: Journal    
DOI: 10.1053/jlts.2001.0070831     Document Type: Article

References (7)

1. Biliary atresia
2. Lifespan in untreated biliary atresia
3. A new operation for "non-correctable" biliary atresia: Hepatic portoenterostomy
4. Treatment of extrahepatic biliary atresia: Results and long-term prognosis after hepatic portoenterostomy
5. A long-term experience with biliary atresia. Reassessment of prognostic factors
6. Choosing a pediatric recipient for orthotopic liver transplantation
7. Causes of late mortality in pediatric liver transplant recipients