TY  -  
T1  - Biliary atresia : growth, bone health and neurocognitive and motor outcome in childhood and adolescence 
SN  -  /  
UR  - URN:ISBN:978-951-51-7677-6; http://hdl.handle.net/10138/335661 
T3  -  
A1  - Ruuska, Satu 
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PB  - Helsingin yliopisto 
Y1  - 2021 
LA  - en 
AB  - Background: Biliary atresia (BA) is a rare cholangiopathy of infancy. Without treatment, inflammation and obstruction of the biliary tracts leads to liver cirrhosis and death within the first 2 years of life. BA is treated with portoenterostomy (PE), in which an exit for bile from the liver is created by attaching a jejunal loop to the porta hepatis. If PE fails, the next treatment option is liver transplantation (LT). Since the development of LT programs in the late 1980s, the long-term outcome... 
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KW  - lääketiede 
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