Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare, multi-system, inflammatory
disease, belonging to the group of anti-neutrophil cytoplasmic antibody (ANCA)-associated …

ABSTRACT Introduction IgG4-related disease (IgG4-RD) is a rare fibro-inflammatory
disease affecting multiple organs. In recent years basic and translational research has …

Background The IgG4-related disease (IgG4-RD) is an immune-mediated disorder with
fibrotic manifestations. However, the transcriptional profiles of immune cell subsets at single …

Autism spectrum disorder (ASD) is a neurodevelopmental disorder affecting approximately
2% of children in the United States. Growing evidence suggests that immune dysregulation …

Abstract IgG4-related disease (IgG4-RD) and idiopathic multicentric Castleman's disease
(iMCD) are both rare systemic immune-mediated disorders. However, the pathogenesis …

Abstract Purpose of Review Neurosarcoidosis is a rare manifestation of sarcoidosis that is
challenging to diagnose. Biopsy confirmation of granulomas is not sufficient, as other …

Immunoglobulin G4-related disease (IgG4-RD) is a systemic fibroinflammatory disease
characterised by multiorgan lymphoplasmacytic infiltration, obliterative phlebitis and …

IgG4-Related Disease (IgG4-RD) is a fibroinflammatory condition characterized by a typical
histopathological pattern (dense lymphoplasmacytic infiltrate with prevalent IgG4+ plasma …

Immunoglobulin G4 (IgG4)–related disease (IgG4-RD) is an immune-mediated
fibrosclerosing disease with tumefactive lesions infiltrated by IgG4-positive plasma cells …

Chronic sclerosing sialadenitis is commonly regarded as a manifestation of IgG4-related
disease. We previously found that a high IgG4 expression or IgG4-related disease could …