Author:
Labrune P.,Myara A.,Hennion C.,Gout J. P.,Trivin F.,Odievre M.
Subject
Genetics (clinical),Genetics
Reference12 articles.
1. Alagille, D. and Odievre, M. Hyperbilirubinemia of the newborn. In Alagille, D. and Odievre, M. (eds.)Liver and Biliary Tract Diseases in Children, Wiley Medical Edit, New York, 1979, pp. 18–42
2. Arias, I. M., Gartner, L. M., Cohen, M., Ben Ezzer, J. and Levi, A. J. Chronic non-hemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency. Clinical, biochemical, pharmacologic and genetic evidence for heterogeneity.Am. J. Med. 47 (1969) 395–409
3. Arias, I. M. Inheritable and congenital hyperbilirubinemia. Models for the study of drug metabolism.N. Engl. J. Med. 285 (1971) 1416–1421
4. Black, M. and Billing, B. H. Hepatic bilirubin UDP glucuronyltransferase activity in liver disease and Gilbert's syndrome.N. Engl. J. Med. 280 (1969) 1266–1271
5. Crigler, J. F. and Gold, N. I. Sodium phenobarbital-induced decrease in serum bilirubin in an infant with congenital non-hemolytic jaundice and kernicterus.J. Clin. Invest. 45 (1966) 998–999
Cited by
16 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献