Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): Review of 80 cases
- 1 February 1987
- journal article
- review article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 110 (2), 195-200
- https://doi.org/10.1016/s0022-3476(87)80153-1
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- Eicosanoid Synthesis in Alagille SyndromeNew England Journal of Medicine, 1986
- Management of paucity of interlobular bile ductsJournal of Hepatology, 1985
- Facies in alagille syndromeThe Journal of Pediatrics, 1984
- Intrahepatic “cholestasis facies”: Is it specific for Alagille syndrome?The Journal of Pediatrics, 1983
- A father and son with cholestasis and peripheral pulmonic stenosisThe Journal of Pediatrics, 1978
- Histopathologic study of the liver in the early cholestatic phase of alpha-1-antitrypsin deficiencyThe Journal of Pediatrics, 1976
- Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmurThe Journal of Pediatrics, 1975
- Arteriohepatic dysplasia: Familial pulmonary arterial stenosis with neonatal liver diseaseArchives of Disease in Childhood, 1973
- Progressive familial cholestatic cirrhosis and bile acid metabolismThe Journal of Pediatrics, 1972
- Trihydroxycoprostanic acid in the duodenal fluid of two children with intrahepatic bile duct anomaliesBiochimica et Biophysica Acta (BBA) - General Subjects, 1972