Reloading Against Rare Liver Diseases
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Gastroenterology,Pediatrics, Perinatology and Child Health
Reference4 articles.
1. Late referral for biliary atresia—missed opportunities for effective surgery;Mieli-Vergani;Lancet,1989
2. alpha1-Antitrypsin deficiency is not an important cause of childhood liver diseases in a multi-ethnic Southeast Asian population;Lee;J Paediatr Child Health,2007
3. Mechanisms of disease: inborn errors of bile acid synthesis;Sundaram;Nat Clin Pract Gastroenterol Hepatol,2008
4. Variable clinical spectrum of the commonest inborn error of bile acid metabolism - 3-hydroxy-5-C27-steroid dehyrdogenase deficiency.;Subramaniam;J Pediatr Gastroenterol Nutr,2010
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1. Neonatal cholestasis in children with Alpha-1-AT deficiency is a risk for earlier severe liver disease with male predominance;Hepatology Communications;2023-12
2. Environmental exposure as a risk-modifying factor in liver diseases: Knowns and unknowns;Acta Pharmaceutica Sinica B;2021-12
3. Longitudinal Outcomes in Young Patients with Alpha-1-Antitrypsin Deficiency with Native Liver Reveal that Neonatal Cholestasis is a Poor Predictor of Future Portal Hypertension;The Journal of Pediatrics;2020-12
4. Clinical profiles and diagnostic challenges in 1158 children with rare hepatobiliary disorders;Pediatric Research;2020-04-12
5. Pathologic Features of Hereditary Cholestatic Diseases;Surgical Pathology Clinics;2018-06
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