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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1965 1
1966 1
1967 1
1970 3
1971 1
1972 1
1973 1
1975 3
1976 1
1977 3
1978 1
1979 1
1981 2
1982 1
1983 2
1985 3
1987 8
1988 12
1989 8
1990 10
1991 10
1992 13
1993 8
1994 6
1995 8
1996 10
1997 9
1998 15
1999 8
2000 12
2001 9
2002 7
2003 17
2004 18
2005 16
2006 17
2007 20
2008 12
2009 16
2010 12
2011 13
2012 22
2013 18
2014 18
2015 30
2016 23
2017 45
2018 25
2019 27
2020 26
2021 25
2022 24
2023 19
2024 8

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587 results

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Page 1
Biliary Atresia - emerging diagnostic and therapy opportunities.
Lendahl U, Lui VCH, Chung PHY, Tam PKH. Lendahl U, et al. EBioMedicine. 2021 Dec;74:103689. doi: 10.1016/j.ebiom.2021.103689. Epub 2021 Nov 12. EBioMedicine. 2021. PMID: 34781099 Free PMC article. Review.
Biliary Atresia is a devastating pediatric cholangiopathy affecting the bile ducts of the liver. ...Finally, we describe current and emerging diagnostic opportunities and recent translation breakthroughs for Biliary Atresia in the area of emerging ther
Biliary Atresia is a devastating pediatric cholangiopathy affecting the bile ducts of the liver. ...Finally, we describe curre
Biliary atresia: A comprehensive review.
Lakshminarayanan B, Davenport M. Lakshminarayanan B, et al. J Autoimmun. 2016 Sep;73:1-9. doi: 10.1016/j.jaut.2016.06.005. Epub 2016 Jun 23. J Autoimmun. 2016. PMID: 27346637 Review.
Biliary atresia presents as an obliterative cholangiopathy with neonatal jaundice and pale stools. ...
Biliary atresia presents as an obliterative cholangiopathy with neonatal jaundice and pale stools. ...
Biliary Atresia in Children: Update on Disease Mechanism, Therapies, and Patient Outcomes.
Antala S, Taylor SA. Antala S, et al. Clin Liver Dis. 2022 Aug;26(3):341-354. doi: 10.1016/j.cld.2022.03.001. Epub 2022 Jun 25. Clin Liver Dis. 2022. PMID: 35868678 Free PMC article. Review.
Biliary atresia is a rare disease but remains the most common indication for pediatric liver transplantation as there are no effective medical therapies to slow progression after diagnosis. Variable contribution of genetic, immune, and environmental factors contribu
Biliary atresia is a rare disease but remains the most common indication for pediatric liver transplantation as there are no e
Neonatal Cholestasis: Updates on Diagnostics, Therapeutics, and Prevention.
Feldman AG, Sokol RJ. Feldman AG, et al. Neoreviews. 2021 Dec 1;22(12):e819-e836. doi: 10.1542/neo.22-12-e819. Neoreviews. 2021. PMID: 34850148 Free PMC article. Review.
Unfortunately, little progress has been made in determining the exact cause of biliary atresia. The median age at the time of the hepatoportoenterostomy procedure is still greater than 60 days; consequently, biliary atresia remains the primary indicati …
Unfortunately, little progress has been made in determining the exact cause of biliary atresia. The median age at the time of …
Maralixibat: First Approval.
Shirley M. Shirley M. Drugs. 2022 Jan;82(1):71-76. doi: 10.1007/s40265-021-01649-0. Drugs. 2022. PMID: 34813049 Free PMC article. Review.
Maralixibat (Livmarli) is an orally-administered, small-molecule ileal bile acid transporter (IBAT) inhibitor being developed by Mirum Pharmaceuticals for the treatment of rare cholestatic liver diseases including Alagille syndrome (ALGS), progressive familial intrahepatic choles …
Maralixibat (Livmarli) is an orally-administered, small-molecule ileal bile acid transporter (IBAT) inhibitor being developed by Mirum Pharm …
Neonatal diagnosis of biliary atresia: a practical review and update.
Brahee DD, Lampl BS. Brahee DD, et al. Pediatr Radiol. 2022 Apr;52(4):685-692. doi: 10.1007/s00247-021-05148-y. Epub 2021 Jul 31. Pediatr Radiol. 2022. PMID: 34331566 Review.
It is critical to diagnose biliary atresia early because failure to treat can result in hepatic fibrosis and death in less than 1 year. In this paper, we review the current diagnostic imaging methods, differential considerations and treatment options for biliary
It is critical to diagnose biliary atresia early because failure to treat can result in hepatic fibrosis and death in less tha …
Neonatal Jaundice.
Abbey P, Kandasamy D, Naranje P. Abbey P, et al. Indian J Pediatr. 2019 Sep;86(9):830-841. doi: 10.1007/s12098-019-02856-0. Epub 2019 Feb 21. Indian J Pediatr. 2019. PMID: 30790186 Review.
The aim of imaging is the timely diagnosis of surgical conditions like biliary atresia and choledochal cysts. Abdominal ultrasound is the first line imaging modality, and Magnetic resonance cholangiopancreatography (MRCP) also has a role, especially in pre-operative …
The aim of imaging is the timely diagnosis of surgical conditions like biliary atresia and choledochal cysts. Abdominal ultras …
Biliary atresia.
Hartley JL, Davenport M, Kelly DA. Hartley JL, et al. Lancet. 2009 Nov 14;374(9702):1704-13. doi: 10.1016/S0140-6736(09)60946-6. Lancet. 2009. PMID: 19914515 Review.
Biliary atresia is a rare disease of infancy, which has changed within 30 years from being fatal to being a disorder for which effective palliative surgery or curative liver transplantation, or both, are available. ...Although much is known about management of bi
Biliary atresia is a rare disease of infancy, which has changed within 30 years from being fatal to being a disorder for which
Biliary Atresia: Clinical and Research Challenges for the Twenty-First Century.
Bezerra JA, Wells RG, Mack CL, Karpen SJ, Hoofnagle JH, Doo E, Sokol RJ. Bezerra JA, et al. Hepatology. 2018 Sep;68(3):1163-1173. doi: 10.1002/hep.29905. Hepatology. 2018. PMID: 29604222 Free PMC article. Review.
Biliary atresia (BA) is a fibroinflammatory disease of the intrahepatic and extrahepatic biliary tree. ...Among host factors, sequence variants in genes related to biliary development and ciliopathies, a notable lack of a cholangiocyte glycocaly
Biliary atresia (BA) is a fibroinflammatory disease of the intrahepatic and extrahepatic biliary tree. ...Among
Recent developments in diagnostics and treatment of neonatal cholestasis.
Feldman AG, Sokol RJ. Feldman AG, et al. Semin Pediatr Surg. 2020 Aug;29(4):150945. doi: 10.1016/j.sempedsurg.2020.150945. Epub 2020 Jul 23. Semin Pediatr Surg. 2020. PMID: 32861449 Free PMC article. Review.
A timely evaluation for its etiology is critical in order to quickly identify treatable causes such as biliary atresia, many of which benefit from early therapy. An expanding group of molecularly defined disorders involving bile formation, canalicular transporters, …
A timely evaluation for its etiology is critical in order to quickly identify treatable causes such as biliary atresia, many o …
587 results