Results 21 to 30 of about 27,104 (199)

Successful Control of Late-Onset Nephrotic Syndrome in FN1-Associated Fibronectin Glomerulopathy: A 17-Year Clinical Course. [PDF]

Nephrology (Carlton)
ABSTRACT Fibronectin glomerulopathy (FNG) is a rare renal disorder characterized by excessive glomerular fibronectin deposition, often associated with variants in the fibronectin 1 (FN1) gene. Clinically, FNG presents with proteinuria, hematuria, and hypertension, and may progress to end‐stage kidney disease.
Kanazawa N, Iyoda M, Abe K, Suzuki T, Shirai Y, Miura K, Honda K, Honda H.   +7 more
europepmc   +2 more sources

WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review

, 2022
BACKGROUND: Intronic WT1 mutations are usually causative of Frasier syndrome with focal segmental glomerulosclerosis as the characteristic nephropathy. Membranoproliferative glomerulonephritis is not commonly associated with disorders of sex development ...
Harraway, James, McManus, Sam, Aldridge, Melanie, Stewart, Anna, Anderson, Erin, Turner, Ross, Borzi, Peter, Trnka, Peter, Burke, John, Coman, David   +9 more
core   +1 more source

What is new in the management of rapidly progressive glomerulonephritis? [PDF]

, 2015
Rapidly progressive glomerulonephritis (RPGN) results from severe crescentic damage to glomeruli and leads to irreversible kidney failure if not diagnosed and managed in a timely fashion.
Greenhall, GHB, G. H. B. Greenhall, Salama, AD, A. D. Salama   +3 more
core   +1 more source

Membranoproliferative glomerulonephritis following tubulointerstitial nephritis is a late manifestation of IgG4-related kidney disease: A distinctive case

Human Pathology: Case Reports, 2019
IgG4-related kidney disease (IgG4RKD) generally presents as an active and chronic fibrosing tubulointerstitial nephritis. Recent reports have described glomerular lesions, typically with IgG4 containing subepithelial/membranous deposits as part of ...
Joichi Usui, Steven P. Salvatore, Mourhege Alsaloum, Alla Goldberg, Sheng Kuo, Surya V. Seshan   +5 more
doaj   +1 more source

Patterns of glomerular disease based on 4-year kidney biopsy material analyzed by light microscopy and immunofluorescence: a retrospective single-center analysis in Poland

Polish Journal of Pathology, 2017
The aim of this study was to assess the epidemiology of different patterns of chronic glomerular diseases based on clinical, histopathological and immunofluorescent findings of glomerulonephritis patients hospitalized in the Department of Nephrology ...
Anna Olewicz-Gawlik, Dorota Sikorska, Agnieszka Pluto-Prądzyńska, Magdalena Roszak, Ilona Idasiak-Piechocka, Krzysztof Pawlaczyk, Andrzej Oko, Aldona Woźniak, Katarzyna Iwanik, Grzegorz Dworacki, Jan Sikora, Jan Żeromski   +11 more
doaj   +1 more source

Membranoproliferative Glomerulonephritis Preceding Non-Hodgkin Lymphoma Recurrence: A Case Report

, 2016
Introduction: Membranoproliferative glomerulonephritis has been reported to occur in association with non-Hodgkin’s lymphoma but there is few information about glomerulonephritis response to the treatment of non-Hodgkin’s lymphoma.
Meltem Sezis Demirci, MS Demirci
core   +2 more sources

Recent advances in the diagnosis and treatment of membranoproliferative glomerulonephritis with monoclonal immunoglobulin deposition

Linchuang shenzangbing zazhi, 2022
Membranoproliferative glomerulonephritis with monoclonal immunoglobulin deposition （MPGNMID） is a rare type of monoclonal gammopathy of renal significance.
Zhang Yuan-yuan, Wang Feng-mei
doaj  

Early recurrence of proliferative glomerulonephritis with monoclonal immunoglobulin deposits in a renal allograft

Saudi Journal of Kidney Diseases and Transplantation, 2016
Proliferative glomerulonephritis with monoclonal immunoglobulin deposits (PGNMIDs) is a clinico-pathologic entity, the recurrence of which in the renal allograft has only recently been described.
Rohit Tewari, Kusum Joshi, Ashwani Kumar, C S Rayat, Rajaram Iyer, Vinay Sakhuja, Mukut Minz   +6 more
doaj   +1 more source

Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases

Scientific Reports, 2020
Galactose-deficient IgA1 (Gd-IgA1) is important in the pathogenesis of IgA nephropathy (IgAN). A Gd-IgA1-specific monoclonal antibody (KM55) has revealed glomerular Gd-IgA1 deposition solely in patients with IgAN and IgA vasculitis with nephritis (IgAV-N)
Shinya Ishiko, Tomoko Horinouchi, Rika Fujimaru, Yuko Shima, Hiroshi Kaito, Ryojiro Tanaka, Shingo Ishimori, Atsushi Kondo, Sadayuki Nagai, Yuya Aoto, Nana Sakakibara, China Nagano, Tomohiko Yamamura, Momoka Yoshimura, Koichi Nakanishi, Junya Fujimura, Naohiro Kamiyoshi, Hiroaki Nagase, Norishige Yoshikawa, Kazumoto Iijima, Kandai Nozu   +20 more
doaj   +1 more source

Membranoproliferative glomerulonephritis [PDF]

, 2020
Abstract The key histological features of membranoproliferative glomerulonephritis (MPGN) are mesangial hypercellularity, endocapillary proliferation, and capillary wall remodelling. There are two main types: (1) immune complex-mediated disease—caused by chronic infection causing persistent antigenaemia (notably hepatitis C ...
Tabitha Turner-Stokes, Mark A. Little
openaire   +2 more sources