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

Year Number of Results
1960 2
1961 1
1965 2
1966 2
1968 1
1969 1
1970 1
1972 2
1973 1
1974 2
1975 1
1976 2
1978 1
1979 6
1981 3
1982 6
1983 1
1984 1
1985 3
1986 2
1987 6
1988 3
1989 8
1990 3
1991 4
1992 4
1993 5
1994 10
1995 3
1996 4
1997 8
1998 6
1999 12
2000 17
2001 6
2002 4
2003 8
2004 8
2005 10
2006 16
2007 9
2008 18
2009 10
2010 18
2011 11
2012 9
2013 11
2014 19
2015 22
2016 14
2017 7
2018 7
2019 6
2020 9
2021 6
2022 5
2023 2
2024 2

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341 results

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Page 1
EASL Clinical Practice Guidelines: The diagnosis and management of patients with primary biliary cholangitis.
European Association for the Study of the Liver. Electronic address: easloffice@easloffice.eu; European Association for the Study of the Liver. European Association for the Study of the Liver. Electronic address: easloffice@easloffice.eu, et al. J Hepatol. 2017 Jul;67(1):145-172. doi: 10.1016/j.jhep.2017.03.022. Epub 2017 Apr 18. J Hepatol. 2017. PMID: 28427765
Primary biliary cholangitis (PBC) is a chronic inflammatory autoimmune cholestatic liver disease, which when untreated will culminate in end-stage biliary cirrhosis. ...Pharmacologic approaches in practice, to reduce the impact of the progressive nature of di …
Primary biliary cholangitis (PBC) is a chronic inflammatory autoimmune cholestatic liver disease, which when untreated will culminate …
Primary biliary cholangitis: pathogenesis and therapeutic opportunities.
Gulamhusein AF, Hirschfield GM. Gulamhusein AF, et al. Nat Rev Gastroenterol Hepatol. 2020 Feb;17(2):93-110. doi: 10.1038/s41575-019-0226-7. Epub 2019 Dec 9. Nat Rev Gastroenterol Hepatol. 2020. PMID: 31819247 Review.
Primary biliary cholangitis is a chronic, seropositive and female-predominant inflammatory and cholestatic liver disease, which has a variable rate of progression towards biliary cirrhosis. ...A current focus of research on nuclear receptor pathway modulation …
Primary biliary cholangitis is a chronic, seropositive and female-predominant inflammatory and cholestatic liver disease, which has a …
Jaundice revisited: recent advances in the diagnosis and treatment of inherited cholestatic liver diseases.
Chen HL, Wu SH, Hsu SH, Liou BY, Chen HL, Chang MH. Chen HL, et al. J Biomed Sci. 2018 Oct 26;25(1):75. doi: 10.1186/s12929-018-0475-8. J Biomed Sci. 2018. PMID: 30367658 Free PMC article. Review.
Accumulation of excessive bile acids and aberrant metabolites results in hepatocellular injury and biliary cirrhosis. Progressive familial intrahepatic cholestasis (PFIC) is the prototype of genetic liver diseases manifesting jaundice in early childhood, progressive …
Accumulation of excessive bile acids and aberrant metabolites results in hepatocellular injury and biliary cirrhosis. Progress …
Primary biliary cirrhosis.
Lindor KD, Gershwin ME, Poupon R, Kaplan M, Bergasa NV, Heathcote EJ; American Association for Study of Liver Diseases. Lindor KD, et al. Hepatology. 2009 Jul;50(1):291-308. doi: 10.1002/hep.22906. Hepatology. 2009. PMID: 19554543 Free article. No abstract available.
The British Society of Gastroenterology/UK-PBC primary biliary cholangitis treatment and management guidelines.
Hirschfield GM, Dyson JK, Alexander GJM, Chapman MH, Collier J, Hübscher S, Patanwala I, Pereira SP, Thain C, Thorburn D, Tiniakos D, Walmsley M, Webster G, Jones DEJ. Hirschfield GM, et al. Gut. 2018 Sep;67(9):1568-1594. doi: 10.1136/gutjnl-2017-315259. Epub 2018 Mar 28. Gut. 2018. PMID: 29593060 Free PMC article.
Primary biliary cholangitis (formerly known as primary biliary cirrhosis, PBC) is an autoimmune liver disease in which a cycle of immune mediated biliary epithelial cell injury, cholestasis and progressive fibrosis can culminate over time in an end-sta …
Primary biliary cholangitis (formerly known as primary biliary cirrhosis, PBC) is an autoimmune liver disease in which …
Cholestatic Itch Management.
Mittal A. Mittal A. Curr Probl Dermatol. 2016;50:142-8. doi: 10.1159/000446057. Epub 2016 Aug 23. Curr Probl Dermatol. 2016. PMID: 27578083 Review.
Cholestatic itch is a feature of numerous hepatobiliary disorders such as primary biliary cirrhosis, primary sclerosing cholangitis, the inherited form of cholestasis, and intrahepatic cholestasis of pregnancy. ...Patients who do not respond to medical therapy …
Cholestatic itch is a feature of numerous hepatobiliary disorders such as primary biliary cirrhosis, primary sclerosing cholan …
Diagnosis and Management of Cirrhosis-Related Osteoporosis.
Santos LA, Romeiro FG. Santos LA, et al. Biomed Res Int. 2016;2016:1423462. doi: 10.1155/2016/1423462. Epub 2016 Oct 20. Biomed Res Int. 2016. PMID: 27840821 Free PMC article. Review.
Despite that, some of these complications are still overlooked and scarcely treated, particularly those that are not related to the liver. This is the case of osteoporosis, the only cirrhosis complication that is not solved after liver transplantation, because bone loss of …
Despite that, some of these complications are still overlooked and scarcely treated, particularly those that are not related to the liver. T …
Diagnosis and management of overlap syndromes.
Bunchorntavakul C, Reddy KR. Bunchorntavakul C, et al. Clin Liver Dis. 2015 Feb;19(1):81-97. doi: 10.1016/j.cld.2014.09.005. Epub 2014 Nov 21. Clin Liver Dis. 2015. PMID: 25454298 Review.
Overlapping features between autoimmune hepatitis (AIH) and cholestatic disorders (primary biliary cirrhosis (PBC), primary sclerosing cholangitis (PSC), or indeterminate cholestasis), so-called overlap syndromes, usually have a progressive course toward cirrhosi …
Overlapping features between autoimmune hepatitis (AIH) and cholestatic disorders (primary biliary cirrhosis (PBC), primary sc …
Fibrate treatment for primary biliary cirrhosis.
Cuperus FJ, Halilbasic E, Trauner M. Cuperus FJ, et al. Curr Opin Gastroenterol. 2014 May;30(3):279-86. doi: 10.1097/MOG.0000000000000056. Curr Opin Gastroenterol. 2014. PMID: 24625898 Review.
PURPOSE OF REVIEW: Primary biliary cirrhosis (PBC) can lead to end-stage liver disease and death. ...The results of phase III studies, such as the Bezafibrate in Combination With Ursodeoxycholic Acid in Primary Biliary Cirrhosis (BEZURSO) trial, are cu …
PURPOSE OF REVIEW: Primary biliary cirrhosis (PBC) can lead to end-stage liver disease and death. ...The results of phase III …
Evidence-based clinical practice guidelines for liver cirrhosis 2015.
Fukui H, Saito H, Ueno Y, Uto H, Obara K, Sakaida I, Shibuya A, Seike M, Nagoshi S, Segawa M, Tsubouchi H, Moriwaki H, Kato A, Hashimoto E, Michitaka K, Murawaki T, Sugano K, Watanabe M, Shimosegawa T. Fukui H, et al. J Gastroenterol. 2016 Jul;51(7):629-50. doi: 10.1007/s00535-016-1216-y. Epub 2016 May 31. J Gastroenterol. 2016. PMID: 27246107 Review.
Nucleoside analogues and peginterferon plus ribavirin combination therapy improve the prognosis of patients with hepatitis B virus related liver cirrhosis and hepatitis C related compensated liver cirrhosis, respectively, although the latter therapy ma …
Nucleoside analogues and peginterferon plus ribavirin combination therapy improve the prognosis of patients with hepatitis B virus re …
341 results