Ausgabe 12/2017
Inhalt (17 Artikel)
Update on investigations pertaining to the pathogenesis of biliary atresia
Alexandra Kilgore, Cara L. Mack
Sclerosing and obstructive cholangiopathy in biliary atresia: mechanisms and association with biliary innate immunity
Kenichi Harada
Unique manifestations of biliary atresia provide new immunological insight into its etiopathogenesis
Toshihiro Muraji, Haruo Ohtani, Satoshi Ieiri
Adjuvant therapy in biliary atresia: hopelessly optimistic or potential for change?
Mark Davenport
Surgical modifications, additions, and alternatives to Kasai hepato-portoenterostomy to improve the outcome in biliary atresia
Shilpa Sharma, Devendra K. Gupta
A review of long-term outcome and quality of life of patients after Kasai operation surviving with native livers
Kenneth K. Y. Wong, Carol W. Y. Wong
Liver transplantation for biliary atresia: a systematic review
Mureo Kasahara, Koji Umeshita, Seisuke Sakamoto, Akinari Fukuda, Hiroyuki Furukawa, Shinji Uemoto
Biliary atresia and liver transplantation: results and thoughts for primary liver transplantation in select patients
Riccardo Superina
Newborn screening for biliary atresia in the United States
Cat Goodhue, Michael Fenlon, Kasper S. Wang
Current management of long-term survivors of biliary atresia: over 40 years of experience in a single center and review of the literature
Hideyuki Sasaki, Hiromu Tanaka, Masaki Nio
Late complications of biliary atresia: hepatopulmonary syndrome and portopulmonary hypertension
Frederick M. Karrer, Bradley J. Wallace, Arturo E. Estrada
Laparoscopic portoenterostomy for biliary atresia: single-center experience and review of literatures
Joel Cazares, Hiroyuki Koga, Hiroshi Murakami, Hiroki Nakamura, Geoffrey Lane, Atsuyuki Yamataka
Prematurity and biliary atresia: a 30-year observational study
Natalie Durkin, Maesha Deheragoda, Mark Davenport