Show simple item record Mieli-Vergani G Vergani D Baumann U Czubkowski P Debray D Dezsőfi, Antal Fischler B Gupte G Hierro L Indolfi G Jahnel J Smets F Verkade HJ Hadzic N 2018-06-25T09:12:24Z 2018-06-25T09:12:24Z 2018
dc.identifier.citation pagination=345-360; journalVolume=66; journalIssueNumber=2; journalTitle=JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION;
dc.identifier.uri doi:10.1097/MPG.0000000000001801
dc.description.abstract Paediatric autoimmune liver disease is characterized by inflammatory liver histology, circulating autoantibodies, and increased levels of IgG, in the absence of a known etiology. Three conditions have a likely autoimmune pathogenesis: autoimmune hepatitis (AIH), autoimmune sclerosing cholangitis, and de novo AIH after liver transplantation. Two types of pediatric AIH are recognized according to seropositivity for smooth muscle and/or antinuclear antibody (AIH-1) or liver kidney microsomal type 1 and/or anti-liver cytosol type 1 antibodies (AIH-2).Pertinent issues addressing the diagnosis, treatment, and long-term follow-up were formulated by a core group of ESPGHAN members. They have commissioned the first authors with execution of this project. Initially, they have performed a systematic literature search on MEDLINE, ResearchGate, and Mendeley databases during the last 30 years and produced a document focusing on prospective and retrospective studies in children. The ESPGHAN core group and ESPGHAN Hepatology Committee members voted on each recommendation, using a formal voting technique.
dc.relation.ispartof urn:issn:0277-2116
dc.title Diagnosis and Management of Pediatric Autoimmune Liver Disease: ESPGHAN Hepatology Committee Position Statement
dc.type Journal Article 2018-06-14T13:29:19Z
dc.language.rfc3066 en
dc.identifier.mtmt 3378636
dc.identifier.wos 000424047200037
dc.identifier.pubmed 29356770
dc.contributor.department SE/AOK/K/I. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem

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