Markers of Cystic Fibrosis—Associated Liver Disease
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Gastroenterology,Pediatrics, Perinatology, and Child Health
Reference15 articles.
1. Recommendations for Management of Liver and Biliary Tract Disease in Cystic Fibrosis
2. High-molecular-mass ("biliary") isoenzyme of alkaline phosphatase and the diagnosis of liver dysfunction in cystic fibrosis.
3. Serum glutathione S-transferase B1 activity as an index of liver function in cystic fibrosis.
4. Transforming Growth Factor-β1 in Plasma and Liver of Children with Liver Disease
5. Prediction of Liver Fibrosis According to Serum Collagen VI Level in Children with Cystic Fibrosis
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1. Diagnosing Cystic Fibrosis in the 21st Century—A Complex and Challenging Task;Diagnostics;2024-04-03
2. Serum bile acids in cystic fibrosis patients – glycodeoxycholic acid as a potential marker of liver disease;Digestive and Liver Disease;2022-01
3. Non-invasive Diagnostic Tests in Cystic Fibrosis-Related Liver Disease: A Diagnostic Test Accuracy Network Meta-Analysis;Frontiers in Medicine;2021-07-27
4. Severe Genotype, Pancreatic Insufficiency and Low Dose of Pancreatic Enzymes Associate with Abnormal Serum Sterol Profile in Cystic Fibrosis;Biomolecules;2021-02-19
5. Cystic Fibrosis and Congenital Anomalies of the Exocrine Pancreas;Pediatric Gastrointestinal and Liver Disease;2021
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