The Kasai portoenterostomy for biliary atresia: a review of a 27-year experience with 81 patients-Reference-Cited by-同舟云学术

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The Kasai portoenterostomy for biliary atresia: a review of a 27-year experience with 81 patients

Published:2003-10 Issue:10 Volume:38 Page:1480-1485
ISSN:0022-3468
Container-title:Journal of Pediatric Surgery
language:en
Short-container-title:Journal of Pediatric Surgery

Author:

Wildhaber Barbara E,Coran Arnold G,Drongowski Robert A,Hirschl Ronald B,Geiger James D,Lelli Joseph L,Teitelbaum Daniel H

Publisher

Elsevier BV

Subject

General Medicine,Pediatrics, Perinatology, and Child Health,Surgery

Reference18 articles.

1. A new operation for “non-correctable” biliary atresia;Kasai;Shuiyutsu,1959

2. Long-term postsurgical outcome of biliary atresia;Okazaki;J Pediatr Surg,1999

3. The outcome of surgery for biliary atresia and the current status of long-term survivors;Nio;Tohoku J Exp Med,1997

4. Early prediction of long-term survival and the timing of liver transplantation after the Kasai operation;Ohhama;J Pediatr Surg,2000

5. Long-term follow-up of patients with biliary atresia successfully treated with hepatic portoenterostomy;Lopez-Santamaria;Pediatr Surg Int,1998

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1. Biliary atresia and liver transplantation in the United States: A contemporary analysis;Liver International;2023-08-07

2. Prognostic factors determining the surgical interference of biliary atresia in Egyptian infants: single-center experience;Egyptian Liver Journal;2023-07-18

3. Biliary Atresia in an Infant Presenting With Kabuki Syndrome: An Autopsy Report and Review of the Literature;Pediatric and Developmental Pathology;2023-03-28

4. Biliary drainage surgery before or after 3 months of life versus primary liver transplantation in children with biliary atresia: comparative cohort study;BJS Open;2023-03-07

5. Prognostic factors and outcomes of Kasai portoenterostomy (KPE): nine-year experience from a lower-middle income country;Pediatric Surgery International;2023-02-28

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