A nephritic puzzle: C3-dominant glomerulonephritis as a sentinel of hidden autoinflammatory disease. [PDF]
Ward RC +4 more
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Single-Center Perspective of Glomerular Pathology in Patients Treated with Checkpoint Inhibitors. [PDF]
Mohan A +7 more
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Surveillance biopsy detects nearly half of early rejections in living donor kidney transplants: an observational study from Nepal. [PDF]
Kafle MP, Thapa S, Shrestha R, Shrees V.
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Pegcetacoplan as a targeted C3 inhibitor in C3 glomerulopathy and immune-complex MPGN. [PDF]
Habib E, Hajj F.
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Proliferative glomerulonephritis with monoclonal immunoglobulin IgG1-κ deposition in a patient with type 1 diabetes: a case report and literature review. [PDF]
Li X +8 more
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Membranoproliferative Glomerulonephritis in Pregnancy
American Journal of the Medical Sciences, 2017Membranoproliferative glomerulonephritis (MPGN) is an uncommon form of glomerulonephritis and it can be particularly difficult to predict outcomes and manage women with this disorder during pregnancy.The management of 3 successful pregnancies in women with MPGN from 1 center and previously described cases from the world literature are reviewed.
Devika Nair, Laura Kidd, N Kevin Krane
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Kaposi's sarcoma (KS) is an unusual tumor principally affecting the skin of the lower extremities. Although the association between KS and renal transplant has been well documented, there are a few KS cases in the literature associated with ...
Mustafa Arici +2 more
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Familial membranoproliferative glomerulonephritis
Nephrology Dialysis Transplantation, 1995Abstract Four and two male sibs of two separate families who had biopsy-proven membranoproliferative glomerulonephritis (MPGN) are presented. In the first family four sibs of the first-degree consanguineous marriage showed the clinical picture of nephrotic syndrome without hypocomplementaemia at initial laboratory findings.
A, Bakkaloglu +4 more
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Idiopathic Membranoproliferative Glomerulonephritis
Annual Review of Medicine, 1980Idiopathic membranoproliferative glomerulonephritis (MPGN) is one iden tifiable form of chronic nephritis characterized by distinctive glomerular morphology. However, it is not known whether MPGN is a single patho genetic entity. It was originally recognized as one type of chronic glomerulonephritis with persistent hypocomplementemia by West et al (1)
Y, Kim, A F, Michael
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