Results 91 to 100 of about 6,839 (215)

Association of glomerular C4d deposition with various demographic data in IgA nephropathy patients; a preliminary study. [PDF]

, 2015
BACKGROUND IgA nephropathy (IgAN) is the most prevalent primary chronic glomerulopathy worldwide. Thus, it is of vital importance to search for factors aggravating the disease progress, monitor disease activity and predict disease-specific therapy ...
Ahmadi, Ali., Bashardoust, Bahman., Mubarak, Muhammed., Nasri, Hamid., Nasri, Parto., Rafieian-Kopaei, Mahmoud.   +5 more
core   +2 more sources

Collapsing Glomerulopathy in Brazil: A Nationwide Descriptive Study

Nephrology, Volume 30, Issue 12, December 2025.
This multicenter study describes the characterization and outcomes of a retrospective cohort of collapsing glomerulopathy cases conducted in Brazil. These findings reinforce the understanding of this rare glomerulopathy. ABSTRACT Aim Collapsing glomerulopathy (CG) is a glomerular disease that progresses rapidly to renal replacement therapy (RRT ...
Marcos Adriano Garcia Campos, Precil Diego Miranda de Meneses Neves, Érico Murilo Monteiro Cutrim, Andressa Monteiro Sodré, João Victor Carvalho, Davi Campos Wanderley, Stanley de Almeida Araújo, Ricardo Miranda Borges, Luiz Fernando Onuchic, Andréia Watanabe, Irene de Lourdes Noronha, Vanessa dos Santos Silva, Igor Denizarde Bacelar Marques, Felipe Leite Guedes, José Bruno de Almeida, Rafael Fernandes Vanderlei Vasco, Antônio Monteiro, Francisco Rasiah Ladchumananandasivam, Orlando Vieira Gomes, Antonio Augusto Lima Teixeira Júnior, Karla Cristina Petruccelli Israel, Denise Maria do Nascimento Costa, Fernanda Pinheiro Martin Tapioca, Epitácio Rafael da Luz Neto, Joyce Santos Lages, Natalino Salgado Filho, Gyl Eanes Barros Silva   +26 more
wiley   +1 more source

Progressive IgA Nephropathy Is Associated With Low Circulating Mannan-Binding Lectin-Associated Serine Protease-3 (MASP-3) and Increased Glomerular Factor H-Related Protein-5 (FHR5) Deposition

, 2017
Introduction IgA nephropathy (IgAN) is characterized by glomerular deposition of galactose-deficient IgA1 and complement proteins and leads to renal impairment.
Constantinou, N, Cook, HT, Hansen, AG, Lomax-Browne, HJ, Medjeral-Thomas, NR, Pickering, MC, Pusey, CD, Thiel, S, Troldborg, A, Willicombe, M   +9 more
core   +2 more sources

Proteinuria After Kidney Transplantation

Pediatric Transplantation, Volume 29, Issue 8, December 2025.
ABSTRACT Proteinuria is a relatively frequent complication in both adults and children after kidney transplantation (40%–80%). It is usually mild and predominantly of tubular origin and is caused mainly by rejection, mTOR inhibitors, or hypertension; however, proteinuria could also be in the nephrotic range and of glomerular origin if caused by the ...
Tomas Seeman, Robert L. Myette, Janusz Feber, Massimiliano Bertacchi, Raja Sekhar Dandamudi, Daniella Levy Erez, Anja Buescher   +6 more
wiley   +1 more source

Mycophenolate Mofetil Treatment of C3 Glomerulopathy

Clinical Journal of the American Society of Nephrology, 2020
C3 glomerulopathy is a relatively newly described and rare disease mediated by dysregulated activity of the alternative complement pathway. Although the light and electron microscopic findings may vary, the disease is defined by immunofluorescence microscopy with glomerular deposition ...
Yonatan Peleg, Gerald B. Appel
openaire   +3 more sources

Glomerular Complement Factor H–Related Protein 5 (FHR5) Is Highly Prevalent in C3 Glomerulopathy and Associated With Renal Impairment

Kidney International Reports, 2019
Introduction: Therapeutic agents that target complement are increasingly available for glomerular diseases. However, the mechanisms linking glomerular complement deposition with inflammation and damage are incompletely understood.
Nicholas R. Medjeral-Thomas, Hilary Moffitt, Hannah J. Lomax-Browne, Nicholas Constantinou, Tom Cairns, H. Terence Cook, Matthew C. Pickering   +6 more
doaj   +1 more source

The Impact of Complement Factor H‐Related Protein Gene Deletions on Kidney Transplantation

Scandinavian Journal of Immunology, Volume 102, Issue 6, December 2025.
In this study, we found that rs7542235 allele G tags a deletion of the CFHR1 gene. We also found that rs6677604 allele A tags a deletion of the whole CFHR3–1 locus. The plasma proteomics studies show that both variants are associated with an altered expression of FH/FHR proteins thus revealing a novel level of intricate regulation of the complement ...
Salla Markkinen, A. Inkeri Lokki, Ilkka Helanterä, Jarmo Ritari, Jukka Partanen, Seppo Meri, Kati Hyvärinen   +6 more
wiley   +1 more source

Case Report of Spontaneous Remission of Biopsy-Proven Idiopathic Immune Complex-Mediated Membranoproliferative Glomerulonephritis

Case Reports in Nephrology and Dialysis, 2017
Membranoproliferative glomerulonephritis (MPGN) is a histopathologic diagnosis causing microscopic hematuria, nephrotic range proteinuria, and chronic renal failure.
Rehan Shah, Mark S. Segal, Michael J. Wilkowski   +2 more
doaj   +1 more source

Glomerulopathy in patients with distal duplication of chromosome 6p [PDF]

, 2016
Background: Duplication of the distal part of chromosome 6p is a rare genetic syndrome. Renal involvement has been reported in the majority of patients, including a wide range of congenital abnormalities of kidney and urinary tract and, occasionally, a ...
Bernaciak, Joanna, Bjerre, Anna, Jankauskienė, Augustina, Koczkowska, Magdalena, Lipska-Ziętkiewicz, Beata S., Schaefer, Franz   +5 more
core   +1 more source

Collapsing Glomerulopathy. A Treatable Disease? [PDF]

, 2008
Renal disease is a relatively common complication in human immunodeficiency virus (HIV) infected patients and has become the fourth leading cause of death in AIDS individuals, immediately following septicaemia, pneumonia and hepatic disease.
Carvalho, D, Carvalho, F, Ferreira, AC, Nolasco, F, Ribeiro dos Santos, J   +4 more
core