Autoimmune hepatitis (AIH) is an unresolving progressive liver disease of unknown etiology
characterized by hypergammaglobulinemia, autoantibodies detection and interface …

Testing for liver-related autoantibodies should be included in the workup of patients with
hepatitis or cholestasis of unknown origin. Although most of these autoantibodies are not …

Primary biliary cholangitis (PBC) is a chronic inflammatory autoimmune cholestatic liver
disease, which when untreated will culminate in end-stage biliary cirrhosis. Diagnosis is …

Paediatric autoimmune liver disease is characterized by inflammatory liver histology,
circulating autoantibodies, and increased levels of IgG, in the absence of a known etiology …

Background Autoimmune hepatitis (AIH) is a disease of unknown aetiology characterised by
interface hepatitis, hypergammaglobulinaemia, circulating autoantibodies and a favourable …

Background Autoimmune hepatitis (AIH), primary biliary cirrhosis (PBC) and primary
sclerosing cholangitis (PSC) all nestle within the family of autoimmune liver diseases …

Overlap syndrome of autoimmune hepatitis (AIH) and primary biliary cholangitis (PBC) is
typically defined as concomitant or serial presentation with clinical features of both of these 2 …

Diagnosis of autoimmune hepatitis (AIH) is in most cases challenging for clinicians as there
is not a single specific laboratory or histological marker to diagnose or exclude the presence …

Background Autoimmune hepatitis (AIH) is a chronic inflammatory liver disease that results
in substantial morbidity and mortality with many unanswered clinical and research …

Autoimmune hepatitis (AIH) is a relatively rare acute or chronic liver disease of unknown
etiology characterized by large heterogeneity. Its distribution is global, covering all ages …