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Biliary atresia: Current concepts and research directions. Summary of a symposium

โœ Scribed by WF Balistreri; R Grand; JH Hoofnagle; FJ Suchy; FC Ryckman; DH Perlmutter; RJ Sokol

Book ID
118686270
Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
227 KB
Volume
23
Category
Article
ISSN
0270-9139

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๐Ÿ“œ SIMILAR VOLUMES

Biliary atresia: Current concepts and re
Biliary atresia: Current concepts and research directions. Summary of a symposium
โœ W F Balistreri; R Grand; J H Hoofnagle; F J Suchy; F C Ryckman; D H Perlmutter; ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 222 KB

Biliary atresia (BA) is the end result of a destructive, rhosis. Until recently, BA was uniformly fatal; liver inflammatory process that affects intra-and extrahetransplantation has altered the inevitability of that patic bile ducts, leading to fibrosis and obliteration of outcome, but at a ''cost''

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โœ Ronald J. Sokol; Ross W. Shepherd; Riccardo Superina; Jorge A. Bezerra; Patricia ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 476 KB ๐Ÿ‘ 1 views

Biliary atresia is the most common cause of end-stage liver disease in the infant and is the leading pediatric indication for liver transplantation in the United States. Earlier diagnosis (<30-45 days of life) is associated with improved outcomes following the Kasai portoenterostomy and longer survi