Results 121 to 130 of about 8,265 (168)

Multi-omics profiling reveals epidermal growth factor as a potential biomarker and therapeutic target in lupus nephritis and ANCA-associated vasculitis with rapidly progressive glomerulonephritis. [PDF]

PLoS One
Xu M, Cheng Q, Xie Y, Chen X, Zhu L, Su W, Du Y, Wu H, Lu K.   +8 more
europepmc   +1 more source

An Unusual Case of Membranoproliferative Glomerulonephritis: Is the Role of Vaccination in Immune Reactivation a Casual or Causal Effect? [PDF]

Reports (MDPI)
Rodríguez Tudero C, Martín Arribas A, Dominguez Davalos M, Jiménez Mayor E, De La Flor JC.   +4 more
europepmc   +1 more source

Delphi Consensus on Surrogate End Points in C3 Glomerulopathy and Primary Immune Complex-Mediated Membranoproliferative Glomerulonephritis. [PDF]

Kidney Int Rep
Caravaca-Fontán F, Fakhouri F, Licht C, Pickering MC, Schaefer F, Wong E.   +5 more
europepmc   +1 more source

Evaluation of clinicopathological features of renal biopsies in non-lupus rheumatic diseases: a university hospital experience. [PDF]

Ren Fail
Sezen M, Yildiz A, Aytaç-Vuruşkan B, Ortaç H, Güllülü M, Ersoy A.   +5 more
europepmc   +1 more source

Clinical Presentation, Treatment Patterns, Burden of Disease, and the Association of Proteinuria with Clinical Outcomes in C3 Glomerulopathy and Primary Immune Complex Membranoproliferative Glomerulonephritis: A Systematic Review.

Nephron
Caravaca-Fontán F, Fakhouri F, Pickering MC, Lionikaite V, Baird A, Horneff R, López-Lázaro L, Quintana-Gallardo L, Rich C.   +8 more
europepmc   +1 more source

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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

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

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, O, Söylemezoglu, K, Tinaztepe, U, Saatçi, F, Söylemezoglu   +4 more
openaire   +2 more sources

[Membranoproliferative glomerulonephritis].

Nihon rinsho. Japanese journal of clinical medicine, 2004
MPGN is characterized by its peculiar histological findings; lobular appearance, cellular and mesangial matrix proliferation and double contoured capillary loops. Based on histomorphalogical pattern, three types are subdivided. MPGN may be primary (in most children) or secondary (in most adults) to chronic infections, cryoglobulinemia or systemic ...
Yoshio, Taguma, Shigemi, Chiba, Hiroshi, Sato   +2 more
  +5 more sources