๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Liver transplantation and the Kasai operation in biliary atresia

โœ Scribed by Barbara A. Stewart; Roberta J. Hall; John R. Lilly


Book ID
117158840
Publisher
Elsevier Science
Year
1988
Tongue
English
Weight
305 KB
Volume
23
Category
Article
ISSN
0022-3468

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Sequential treatment of biliary atresia
โœ Jean-Bernard Otte; Jean De Ville De Goyet; Raymond Reding; Victoria Hausleithner ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 864 KB

Biliary atresia is the most frequent cause of chronic cholestasis in infants. When left untreated, this condition leads to death from liver insufficiencywithin the first 2 yr of life. The modern therapeutic approach consists of a sequential strategy with Kasai portoenterostomy as a first step and, i

Outcome of living donor liver transplant
โœ Yusuke Kyoden; Sumihito Tamura; Yasuhiko Sugawara; Noriyo Yamashiki; Yuichi Mats ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 123 KB ๐Ÿ‘ 2 views

Previous reports described the effectiveness of living donor liver transplantation (LDLT) for post-Kasai biliary atresia (BA) in the pediatric population. Information on the outcome of LDLT in patients that have reached adulthood after the Kasai procedure, however, is limited. A recent report postul