Hepatobiliary insufficiency-candidate of transplantation newborns and anesthesia (two cases); [Hepatobilier yetmezlikli-transplantasyon adayi neonatal olgular ve anestezi]
| dc.contributor.author | Öztürk T. | |
| dc.contributor.author | Bulut S. | |
| dc.contributor.author | Toprak V. | |
| dc.contributor.author | Tezcan Keleş G. | |
| dc.date.accessioned | 2025-04-10T11:16:22Z | |
| dc.date.available | 2025-04-10T11:16:22Z | |
| dc.date.issued | 2008 | |
| dc.description.abstract | Biliary atresia (BA) is the most common and important neonatal hepatobiliary disorder and is seen in 1 in 8.000 to 1 in 18.000. Consequently, 70-80 % of BA patients will eventually require liver transplantation, approximately half in the first 2 y of life. Early diagnosis and therapy is essential especially for the survival of patients with biliary atresia. | |
| dc.identifier.uri | http://hdl.handle.net/20.500.14701/51772 | |
| dc.title | Hepatobiliary insufficiency-candidate of transplantation newborns and anesthesia (two cases); [Hepatobilier yetmezlikli-transplantasyon adayi neonatal olgular ve anestezi] | |
| dc.type | Article |