Results 151 to 160 of about 27,104 (199)

Single-Center Perspective of Glomerular Pathology in Patients Treated with Checkpoint Inhibitors. [PDF]

open access: yesKidney Int Rep
Mohan A   +7 more
europepmc   +1 more source

Membranoproliferative Glomerulonephritis in Pregnancy

American Journal of the Medical Sciences, 2017
Membranoproliferative 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
exaly   +3 more sources

A Case of Kaposi's Sarcoma Following Treatment of Membranoproliferative Glomerulonephritis and a Review of the Literature

open access: yesRenal Failure, 2007
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
exaly   +2 more sources

Familial membranoproliferative glomerulonephritis

Nephrology Dialysis Transplantation, 1995
Abstract 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
openaire   +2 more sources

Idiopathic Membranoproliferative Glomerulonephritis

Annual Review of Medicine, 1980
Idiopathic 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
openaire   +2 more sources

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