Successful Treatment with Colestimide for a Bout of Cholestasis in a Japanese Patient with Benign Recurrent Intrahepatic Cholestasis Caused by ATP8B1 Mutation
Author:
Affiliation:
1. Department of Medicine, Teikyo University School of Medicine
2. Department of Pediatrics, Teikyo University School of Medicine
3. Department of Pathology, Teikyo University School of Medicine
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
http://www.jstage.jst.go.jp/article/internalmedicine/47/7/47_7_599/_pdf
Reference10 articles.
1. Benign recurrent intrahepatic cholestasis
2. A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis
3. Progressive familial intrahepatic cholestasis, type 1, is associated with decreased farnesoid X receptor activity
4. Benign recurrent intrahepatic cholestasis: A long-term follow-up study of two patients
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1. Clinicopathologic Features, Genetics, Treatment, and Long-Term Outcomes in Japanese Children and Young Adults with Benign Recurrent Intrahepatic Cholestasis: A Multicenter Study;Journal of Clinical Medicine;2023-09-15
2. Long‐Term Colestyramine Treatment Prevents Cholestatic Attacks in Refractory Benign Recurrent Intrahepatic Cholestasis Type 1 Disease;Hepatology;2021-06-28
3. AN UNUSUAL CASE OF BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS;INDIAN JOURNAL OF APPLIED RESEARCH;2021-01-01
4. Assessment of Adenosine Triphosphatase Phospholipid Transporting 8B1 (ATP8B1) Function in Patients With Cholestasis With ATP8B1 Deficiency by Using Peripheral Blood Monocyte‐Derived Macrophages;Hepatology Communications;2020-09-26
5. Successful treatment with 4‐phenylbutyrate in a patient with benign recurrent intrahepatic cholestasis type 2 refractory to biliary drainage and bilirubin absorption;Hepatology Research;2015-09-15
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