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IgG4-Related Kidney Disease and IgG4-Related Retroperitoneal Fibrosis
Seminars in Liver Disease, 2016Immunoglobulin G4-related kidney disease (IgG4-RKD) is the collective name encompassing renal parenchymal and renal pelvic lesions. The hallmark of renal parenchymal lesions of IgG4-related disease is plasma cell-rich tubulointerstitial nephritis with numerous IgG4-positive plasma cells and characteristic fibrosis.
Mitsuhiro, Kawano, Kazunori, Yamada
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Diagnostic Histopathology, 2012
IgG4-related disease (IgG4-RD) is a recently recognized systemic autoimmune disease that has received increased attention in the literature in the past several years. Renal involvement can take several forms, which are described in this review.IgG4-RD may affect the kidney in various patterns. IgG4-related tubulointerstitial nephritis (TIN), presenting
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IgG4-related disease (IgG4-RD) is a recently recognized systemic autoimmune disease that has received increased attention in the literature in the past several years. Renal involvement can take several forms, which are described in this review.IgG4-RD may affect the kidney in various patterns. IgG4-related tubulointerstitial nephritis (TIN), presenting
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IgG4-Related Ophthalmic Disease
New England Journal of Medicine, 2022Yi-Min Huang, Pei-Hsuan Lin
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[IgG4-related systemic disease/systemic IgG4-related disease].
Rinsho byori. The Japanese journal of clinical pathology, 2010IgG4-related systemic disease/systemic IgG4-related disease has been established as a new systemic disease entity. It is characterized by high serum IgG4 concentrations and abundant IgG4-bearing plasma cell infiltration in the involved organs. The chronic inflammation can attack lacrimal glands, salivary glands, the thyroid, lung, pancreas, kidney, and
Motohisa, Yamamoto +2 more
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