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

Year Number of Results
1997 2
1998 3
1999 3
2000 3
2001 1
2002 2
2003 7
2004 3
2005 5
2006 5
2007 5
2008 9
2009 6
2010 8
2011 5
2012 11
2013 16
2014 12
2015 11
2016 11
2017 10
2018 14
2019 6
2020 12
2021 13
2022 9
2023 9
2024 4

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186 results

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Page 1
Diagnosis and management of autoimmune hepatitis.
Muratori L, Lohse AW, Lenzi M. Muratori L, et al. BMJ. 2023 Feb 6;380:e070201. doi: 10.1136/bmj-2022-070201. BMJ. 2023. PMID: 36746473 Review.
A specific set of autoantibodies, increased IgG concentrations, and histological demonstration of interface hepatitis and periportal necrosis are the diagnostic hallmarks of autoimmune hepatitis. ...
A specific set of autoantibodies, increased IgG concentrations, and histological demonstration of interface hepatitis and peri …
Autoimmune hepatitis: Challenges and novelties.
Olivas I, Rodríguez-Tajes S, Londoño MC. Olivas I, et al. Med Clin (Barc). 2022 Sep 23;159(6):289-298. doi: 10.1016/j.medcli.2022.04.004. Epub 2022 Jun 7. Med Clin (Barc). 2022. PMID: 35688746 Review. English, Spanish.
It is characterized by increase in transaminase and immunoglobulin G levels, autoantibodies, and portal inflammatory infiltrate with interface hepatitis in the liver biopsy. The treatment is based on the combination of corticoids and azathioprine, but 20-40% of pati …
It is characterized by increase in transaminase and immunoglobulin G levels, autoantibodies, and portal inflammatory infiltrate with inte
Autoimmune Hepatitis: 2019 Update.
Tanaka A. Tanaka A. Gut Liver. 2020 Jul 15;14(4):430-438. doi: 10.5009/gnl19261. Gut Liver. 2020. PMID: 32301319 Free PMC article. Review.
Autoimmune hepatitis (AIH) is a chronic inflammatory liver disease, characterized by the elevation of aminotransferases, presence of anti-nuclear antibody or anti-smooth muscle antibody, elevated immunoglobulin G (IgG), and interface hepatitis/plasma-lymphocytic inf …
Autoimmune hepatitis (AIH) is a chronic inflammatory liver disease, characterized by the elevation of aminotransferases, presence of anti-nu …
Autoimmune hepatitis.
Mieli-Vergani G, Vergani D, Czaja AJ, Manns MP, Krawitt EL, Vierling JM, Lohse AW, Montano-Loza AJ. Mieli-Vergani G, et al. Nat Rev Dis Primers. 2018 Apr 12;4:18017. doi: 10.1038/nrdp.2018.17. Nat Rev Dis Primers. 2018. PMID: 29644994 Review.
The diagnosis of AIH relies on increased serum transaminase and immunoglobulin G levels, presence of autoantibodies and interface hepatitis on liver histology. AIH arises in genetically predisposed individuals when a trigger, such as exposure to a virus, leads to a …
The diagnosis of AIH relies on increased serum transaminase and immunoglobulin G levels, presence of autoantibodies and interface
New Treatment Paradigms in Primary Biliary Cholangitis.
Levy C, Manns M, Hirschfield G. Levy C, et al. Clin Gastroenterol Hepatol. 2023 Jul;21(8):2076-2087. doi: 10.1016/j.cgh.2023.02.005. Epub 2023 Feb 19. Clin Gastroenterol Hepatol. 2023. PMID: 36809835 Free article. Review.
Primary biliary cholangitis (PBC) is an archetypal autoimmune disease. Chronic lymphocytic cholangitis is associated with interface hepatitis, ductopenia, cholestasis, and progressive biliary fibrosis. ...
Primary biliary cholangitis (PBC) is an archetypal autoimmune disease. Chronic lymphocytic cholangitis is associated with interface
Pathology of autoimmune hepatitis.
Covelli C, Sacchi D, Sarcognato S, Cazzagon N, Grillo F, Baciorri F, Fanni D, Cacciatore M, Maffeis V, Guido M. Covelli C, et al. Pathologica. 2021 Jun;113(3):185-193. doi: 10.32074/1591-951X-241. Pathologica. 2021. PMID: 34294936 Free PMC article. Review.
It is characterized by hypergammaglobulinemia, circulating autoantibodies, interface hepatitis on liver histology and a favourable response to immunosuppression. ...
It is characterized by hypergammaglobulinemia, circulating autoantibodies, interface hepatitis on liver histology and a favour …
Overlap Syndromes.
Chazouillères O. Chazouillères O. Dig Dis. 2015;33 Suppl 2:181-7. doi: 10.1159/000440831. Epub 2015 Dec 7. Dig Dis. 2015. PMID: 26641819
It remains unclear whether this syndrome forms a distinct entity or is a variant of PBC, PSC or AIH. KEY MESSAGES: Moderate to severe interface hepatitis is a fundamental component and histology is vital in evaluating patients with overlap presentation. ...
It remains unclear whether this syndrome forms a distinct entity or is a variant of PBC, PSC or AIH. KEY MESSAGES: Moderate to severe int
Consensus recommendations for histological criteria of autoimmune hepatitis from the International AIH Pathology Group: Results of a workshop on AIH histology hosted by the European Reference Network on Hepatological Diseases and the European Society of Pathology: Results of a workshop on AIH histology hosted by the European Reference Network on Hepatological Diseases and the European Society of Pathology.
Lohse AW, Sebode M, Bhathal PS, Clouston AD, Dienes HP, Jain D, Gouw ASH, Guindi M, Kakar S, Kleiner DE, Krech T, Lackner C, Longerich T, Saxena R, Terracciano L, Washington K, Weidemann S, Hübscher SG, Tiniakos D. Lohse AW, et al. Liver Int. 2022 May;42(5):1058-1069. doi: 10.1111/liv.15217. Epub 2022 Mar 12. Liver Int. 2022. PMID: 35230735
AIH is also considered likely if there is predominantly lobular hepatitis with or without centrilobular necroinflammation and at least one of the following features: portal lymphoplasmacytic hepatitis, interface hepatitis or portal-based fibrosis, in the absence of …
AIH is also considered likely if there is predominantly lobular hepatitis with or without centrilobular necroinflammation and at least one o …
Diagnostic approach to autoimmune hepatitis.
Muratori P, Lenzi M, Cassani F, Lalanne C, Muratori L. Muratori P, et al. Expert Rev Clin Immunol. 2017 Aug;13(8):769-779. doi: 10.1080/1744666X.2017.1327355. Epub 2017 May 17. Expert Rev Clin Immunol. 2017. PMID: 28480763 Review.
Precision medicine for autoimmune hepatitis.
Chen RL, Wang QX, Ma X. Chen RL, et al. J Dig Dis. 2019 Jul;20(7):331-337. doi: 10.1111/1751-2980.12786. Epub 2019 Jul 7. J Dig Dis. 2019. PMID: 31099976 Review.
AIH is characterized by hypergammaglobulinemia, elevation of serum autoantibodies and transaminases, and interface hepatitis. Personalized therapy is necessary in AIH because of its heterogeneity in clinical manifestations. ...
AIH is characterized by hypergammaglobulinemia, elevation of serum autoantibodies and transaminases, and interface hepatitis. …
186 results