Matches in DBpedia 2015-10 for { ?s ?p "IgG4-related disease (IgG4-RD) is a relapsing–remitting immune-mediated fibroinflammatory disease characterised by: a tendency to mass forming, tissue-destructive lesions in multiple sites; a prompt response usually to steroids; a characteristic histopathological appearance; and elevated serum IgG4 concentrations in approximately 60–70% of people during an acute phase.The disease, which was formerly also known as IgG4-related systemic disease, is so named because plasma cells producing the antibody subtype IgG4 are present in large amounts on tissue samples from involved organs, and because IgG4 antibody levels in the bloodstream are often elevated.Inflammation results in fibrosis, the deposition of connective tissue, in affected anatomical sites which can lead to organ dysfunction, or even organ failure, if not treated.Early detection is important to avoid organ damage and potentially serious complications."@en }
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- IgG4-related_disease abstract "IgG4-related disease (IgG4-RD) is a relapsing–remitting immune-mediated fibroinflammatory disease characterised by: a tendency to mass forming, tissue-destructive lesions in multiple sites; a prompt response usually to steroids; a characteristic histopathological appearance; and elevated serum IgG4 concentrations in approximately 60–70% of people during an acute phase.The disease, which was formerly also known as IgG4-related systemic disease, is so named because plasma cells producing the antibody subtype IgG4 are present in large amounts on tissue samples from involved organs, and because IgG4 antibody levels in the bloodstream are often elevated.Inflammation results in fibrosis, the deposition of connective tissue, in affected anatomical sites which can lead to organ dysfunction, or even organ failure, if not treated.Early detection is important to avoid organ damage and potentially serious complications.".
- IgG4-related_disease comment "IgG4-related disease (IgG4-RD) is a relapsing–remitting immune-mediated fibroinflammatory disease characterised by: a tendency to mass forming, tissue-destructive lesions in multiple sites; a prompt response usually to steroids; a characteristic histopathological appearance; and elevated serum IgG4 concentrations in approximately 60–70% of people during an acute phase.The disease, which was formerly also known as IgG4-related systemic disease, is so named because plasma cells producing the antibody subtype IgG4 are present in large amounts on tissue samples from involved organs, and because IgG4 antibody levels in the bloodstream are often elevated.Inflammation results in fibrosis, the deposition of connective tissue, in affected anatomical sites which can lead to organ dysfunction, or even organ failure, if not treated.Early detection is important to avoid organ damage and potentially serious complications.".