"Biliary Atresia" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Progressive destruction or the absence of all or part of the extrahepatic BILE DUCTS, resulting in the complete obstruction of BILE flow. Usually, biliary atresia is found in infants and accounts for one third of the neonatal cholestatic JAUNDICE.
| Descriptor ID |
D001656
|
| MeSH Number(s) |
C06.130.120.123 C06.198.125 C16.131.314.125
|
| Concept/Terms |
Biliary Atresia- Biliary Atresia
- Biliary Atresia, Extrahepatic
- Atresia, Extrahepatic Biliary
- Biliary Atresias, Extrahepatic
- Extrahepatic Biliary Atresia
- Extrahepatic Biliary Atresias
- Atresia, Biliary
|
Below are MeSH descriptors whose meaning is more general than "Biliary Atresia".
Below are MeSH descriptors whose meaning is more specific than "Biliary Atresia".
This graph shows the total number of publications written about "Biliary Atresia" by people in this website by year, and whether "Biliary Atresia" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
| 1999 | 1 | 0 | 1 |
| 2000 | 1 | 0 | 1 |
| 2001 | 1 | 1 | 2 |
| 2002 | 0 | 1 | 1 |
| 2003 | 1 | 0 | 1 |
| 2004 | 1 | 1 | 2 |
| 2005 | 1 | 0 | 1 |
| 2006 | 2 | 1 | 3 |
| 2007 | 3 | 0 | 3 |
| 2008 | 1 | 1 | 2 |
| 2010 | 1 | 2 | 3 |
| 2011 | 5 | 0 | 5 |
| 2012 | 4 | 0 | 4 |
| 2013 | 6 | 0 | 6 |
| 2014 | 4 | 0 | 4 |
| 2015 | 2 | 1 | 3 |
| 2016 | 5 | 0 | 5 |
| 2017 | 3 | 1 | 4 |
| 2018 | 6 | 0 | 6 |
| 2019 | 4 | 0 | 4 |
| 2020 | 6 | 0 | 6 |
| 2021 | 4 | 0 | 4 |
| 2022 | 3 | 0 | 3 |
| 2023 | 8 | 0 | 8 |
| 2024 | 2 | 0 | 2 |
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Below are the most recent publications written about "Biliary Atresia" by people in Profiles.
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Postoperative outcomes of acute-on-chronic liver failure in infants and children with biliary atresia. Pediatr Transplant. 2024 May; 28(3):e14736.
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Protein biomarkers GDF15 and FGF21 to differentiate mitochondrial hepatopathies from other pediatric liver diseases. Hepatol Commun. 2024 Jan 01; 8(1).
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Biliary atresia and liver transplantation in the United States: A contemporary analysis. Liver Int. 2023 10; 43(10):2198-2209.
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Elevated bile acids are associated with left ventricular structural changes in biliary atresia. Hepatol Commun. 2023 05 01; 7(5).
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Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants. Am J Med Genet A. 2023 06; 191(6):1546-1556.
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Characteristics of infections and their risk factors in children with biliary atresia. Clin Res Hepatol Gastroenterol. 2023 04; 47(4):102109.
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Disparate Intent-to-Treat Outcomes for Pediatric Liver Transplantation Based on Indication. Can J Gastroenterol Hepatol. 2023; 2023:2859384.
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Biliary Atresia Remnants Revisited: Myogenesis, Hepatic Duct-Like Structures, and Fate of Peribiliary Glands. Pediatr Dev Pathol. 2023 May-Jun; 26(3):259-272.
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Serum bile acids as a prognostic biomarker in biliary atresia following Kasai portoenterostomy. Hepatology. 2023 03 01; 77(3):862-873.
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Acute-on-chronic liver failure before liver transplantation does not impact post-transplant survival in children with biliary atresia. Liver Transpl. 2023 05 01; 29(5):485-496.