Treatment with an ileal bile acid transporter inhibitor in patients with TJP2 deficiency
Author:
Publisher
Elsevier BV
Subject
Gastroenterology,Hepatology
Reference16 articles.
1. Newer variants of progressive familial intrahepatic cholestasis;Vinayagamoorthy;World J Hepatol,2021
2. Cholestatic jaundice in infancy: struggling with many old and new phenotypes;Mandato;Ital J Pediatr,2019
3. OMIM, Cholestasis Progressive Familial Intrahepatic, PFIC4. Available from: https://www.omim.org/entry/615878.
4. Systematic review of progressive familial intrahepatic cholestasis;Baker;Clin Res Hepatol Gastroenterol,2019
5. Pediatric cholestatic liver disease: review of bile acid metabolism and discussion of current and emerging therapies;Kriegermeier;Front Med (Lausanne),2020
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1. IBAT inhibitors in pediatric cholestatic liver diseases: Transformation on the horizon?;Hepatology;2024-07-25
2. Emerging drugs for the treatment of progressive familial intrahepatic cholestasis: a focus on phase II and III trials;Expert Opinion on Emerging Drugs;2024-07-04
3. Odevixibat as an adjunctive treatment for refractory pruritus in rare variants of cholestatic liver disease;JPGN Reports;2024-04-04
4. Genotype correlates with clinical course and outcome of children with tight junction protein 2 (TJP2) deficiency–related cholestasis;Hepatology;2024-03-06
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