Alagille syndrome: understanding the genotype-phenotype relationship and its potential therapeutic impact
Author:
Affiliation:
1. Division of Gastroenterology, Department of Pediatrics, Stanford University School of Medicine, Palo Alto, CA, USA
2. Division of Pediatric Gastroenterology, Department of Pediatrics, Oregon Health & Science University, Portland, OR, USA
Publisher
Informa UK Limited
Subject
Gastroenterology,Hepatology
Link
https://www.tandfonline.com/doi/pdf/10.1080/17474124.2023.2255518
Reference66 articles.
1. L’atresie des voies biliaires intrahepatiques avec voies biliaires extrahepatiques permeables chez l’enfant;Alagille D;J Par Pediatr,1969
2. Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): Review of 80 cases
3. Spinner NB, Gilbert MA, Loomes KM, et al. Alagille Syndrome. In: Adam M, Mirzaa G, Pagon R, Wallace S, Bean L, Gripp K Amemiya A editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 2000 May 19 [updated 2019 Dec 12]. p. 1993–2023
4. Alagille Syndrome
5. Alagille syndrome: pathogenesis, diagnosis and management
Cited by 1 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
1. Clinical, pathological and genetic characteristics of 17 unrelated children with Alagille Syndrome;BMC Pediatrics;2024-08-20
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