Serum glutathione S-transferase B1 activity as an index of liver function in cystic fibrosis.

Author:

Rattenbury J M,Taylor C J,Heath P K,Howie A F,Beckett G J

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference21 articles.

1. Hepatobiliary disease in cystic fibrosis: a survey of current issues and concepts;Roy, C.C.; Weber, A.M.; Morin, C.L.; Lepage, G.; Brisson, G.; Yousef, I.;Jf Pediatr Gastroenterol Nutr,1982

2. Prevalence of liver disease in cystic fibrosis;Scott-Jupp, R.; Lama, M.; Tanner, M.S.;Arch Dis Child,1991

3. Fibrocystic Disease of the Pancreas. A congenital disorder of mucus production-mucosis;Bodian, M.,1952

4. Hepatic changes in young infants with cystic fibrosis: Possible relation to focal biliary cirrhosis;Oppenheimer, E.H.; Esterly, JR;Jf Pediatr,1975

5. The liver and biliary system;Psacharopoulos, H.T.; Mowat, A.P.,1983

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2. Quelle est la prise en charge de l'atteinte hépatobiliaire au cours de la mucoviscidose?;Archives de Pédiatrie;2003-08

3. Markers of Cystic Fibrosis—Associated Liver Disease;Journal of Pediatric Gastroenterology and Nutrition;2001-04

4. Markers of Cystic Fibrosis—Associated Liver Disease;Journal of Pediatric Gastroenterology and Nutrition;2001-04

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