Presentation of Progressive Familial Intrahepatic Cholestasis Type 3 Mimicking Wilson Disease: Molecular Genetic Diagnosis and Response to Treatment-Reference-Cited by-同舟云学术

Presentation of Progressive Familial Intrahepatic Cholestasis Type 3 Mimicking Wilson Disease: Molecular Genetic Diagnosis and Response to Treatment

Published:2015 Issue:3 Volume:18 Page:202
ISSN:2234-8646
Container-title:Pediatric Gastroenterology, Hepatology & Nutrition
language:en
Short-container-title:Pediatr Gastroenterol Hepatol Nutr

Author:

Boga Salih¹,Jain Dhanpat²,Schilsky Michael L.¹

Affiliation:

1. Division of Digestive Diseases and Section of Transplantation and Immunology, Department of Medicine and Surgery, Yale University School of Medicine, New Haven, CT, USA.

2. Department of Pathology, Yale University School of Medicine, New Haven, CT, USA.

Publisher

The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition

Subject

Gastroenterology,Hepatology,Pediatrics, Perinatology and Child Health

Link

https://synapse.koreamed.org/pdf/10.5223/pghn.2015.18.3.202

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2. Rhodanine Stain Improves Utility of Leipzig Score to Diagnose Hepatic Wilson’s Disease in Noncholestatic Patients with Fibrosis;Gastroenterology, Hepatology and Endoscopy Practice;2023-12-28

3. Current and Emerging Issues in Wilson’s Disease;New England Journal of Medicine;2023-09-07

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5. Clinical and genetic characterization of pediatric patients with progressive familial intrahepatic cholestasis type 3 (PFIC3): identification of 14 novel ABCB4 variants and review of the literatures;Orphanet Journal of Rare Diseases;2022-12-22