Results 11 to 20 of about 21,254 (226)

Increased retinal drusen in IgA glomerulonephritis are further evidence for complement activation in disease pathogenesis

Scientific Reports, 2022
Drusen are retinal deposits comprising cell debris, immune material and complement that are characteristic of macular degeneration but also found in glomerulonephritis.
Langsford, David, Sandhu, K, Catran, Andrew, Langsford, D, Ierino, F, Mack, H, Colville, Deb, Barit, David, Mack, Heather, Catran, A, Savige, J, Skene, Alison, Savige, Judy, Harraka, P, Colville, D, Pianta, Timothy, Akom, S, Wightman, T, Pianta, T, Harraka, P., Akom, Sarah, Wightman, Tony, Ierino, Frank, Skene, A, Barit, D, Sandhu, Kieran   +25 more
core   +2 more sources

Immunoglobulin A (IgA) associated glomerulonephritis

Kidney International, 1973
Immunoglobulin A (IgA) associated glomerulonephritis. Adequate tissue from 153 glomerulonephritic patients was examined by direct immunofluorescence for glomerular-bound immunoglobulins, β1C, and fibrinogen. Ninety-six specimens contained immunoglobulins; 15 (16%) that contained significant amounts of IgA were from patients without systemic lupus ...
Lowance, David C., Mullins, James D., McPhaul, John J.   +2 more
openaire   +3 more sources

Development of anti-glomerular basement membrane glomerulonephritis during the course of IgA nephropathy: a case report

BMC Nephrology, 2019
Background Anti-glomerular basement membrane (GBM) glomerulonephritis does not usually coexist with another glomerulonephritis such as IgA nephropathy.
Shuuhei Komatsu, Muneharu Yamada, Kentaro Sugisaki, Taito Oshima, Noriko Yoshikawa, Tadasu Kojima, Go Hirose, Tomohiro Tomiyasu, Takashi Oda   +8 more
core   +2 more sources

IgA vasculitis in an adult diabetic male with rapidly progressive glomerulonephritis: A case study

Journal of Acute Disease
Rationale: IgA vasculitis or Henoch-Schonlein purpura is an immune complex mediated small vessel vasculitis characterized by clinical triad of arthritis, palpable purpura and gastrointestinal symptoms.
Varsha Luthra, Anjali Yadav, Aprajita Garg, Tarun Chaudhary, Monica Gupta   +4 more
core   +2 more sources

Clinicopathologic features of infection-related glomerulonephritis with IgA deposits: a French Nationwide study

Diagnostic Pathology, 2020
International audienceAbstract Background Infection-related glomerulonephritis with IgA deposits (IRGN-IgA) is a rare disease but it is increasingly reported in the literature. Data regarding epidemiology and outcome are lacking, especially in Europe. We
Eymieux, Sébastien, Rabant, Marion, Rivalan, Joseph, Karras, Alexandre, Cornec-Le Gall, Emilie, Ducloux, Didier, Deltombe, Clément, Jaulerry, Charlotte, Albert, Catherine, Hummel, Aurélie, Barbet, Christelle, Renaudin, Karine, Miquelestorena-Standley, Elodie, Halimi, Jean-Michel, Croué, Anne, Buob, David, Felix, Sophie, Crepin, Thomas, Rabot, Nolwenn, Garrouste, Cyril, Doucet, Laurent, Pourreau, François, Rioux-Leclerc, Nathalie, Szlavik, Nora, Goujon, Jean-Michel, Nochy, Dominique, Machet, Marie-Christine, Blanchard, Emmanuelle, Cousin, Maud   +28 more
core   +2 more sources

Rapidly progressive glomerulonephritis due to anti-glomerular basement membrane disease accompanied by IgA nephropathy: An unusual association

Saudi Journal of Kidney Diseases and Transplantation, 2017
Anti-glomerular basement membrane (anti-GBM) disease is a systemic autoimmune disorder characterized by circulating IgG antibodies (rarely IgA and IgM) to the carboxyterminal, noncollagenous 1 (NC1) domain of type IV collagen of GBM also known as ...
N D Srinivasa Prasad, G Chandramohan, Ishwarya Annamalai, Edwin Fernando, S Sujith   +4 more
core   +2 more sources

Acute glomerulonephritis with large confluent IgA-dominant deposits associated with liver cirrhosis [PDF]

PLoS ONE, 2018
BackgroundSmall glomerular IgA deposits have been reported in patients with liver cirrhosis, mainly as an incidental finding in autopsy studies. We recently encountered nine cirrhotic patients who presented with acute proliferative glomerulonephritis ...
Tibor Nadasdy (5081672), Isabelle Ayoub, Sergey V. Brodsky, Isabelle Ayoub (800894), Jessica Hemminger, Anjali A. Satoskar (5081669), Sergey V Brodsky, Sergey V. Brodsky (5081675), Vidya Arole, Anjali A. Satoskar, Jessica Hemminger (3431918), Tibor Nadasdy, Anjali A Satoskar, Vidya Arole (4656961)   +13 more
core   +2 more sources

Rapidly Progressive Glomerulonephritis Secondary to IgA Nephropathy in a Patient with Systemic Lupus Erythematosus

Case Reports in Nephrology, 2019
Lupus nephritis is a common manifestation of systemic lupus erythematosus (SLE). IgA nephropathy is a common type of primary glomerulonephritis. Renal manifestations in SLE patients are often due to lupus nephritis; however, renal diseases unrelated to ...
Amol M. Patel, Luan D. Truong, Lily Anne Romero Karam, Juan M. Gonzalez, Stephanie C. Fuentes Rojas, Warren E. Redfearn   +5 more
core   +2 more sources

Clinicopathological and prognostic study of IgA-dominant postinfectious glomerulonephritis

BMC Nephrology, 2021
Background The clinicopathological and prognostic features of IgA-dominant postinfectious glomerulonephritis and its difference from the primary IgA nephropathy remains to be investigated.
Ziyuan Huang, Bo Chen, Ying Zhou, Yan Liang, Wenxian Qiu, Yinqiu Lv, Xiaokai Ding, Ji Zhang, Chaosheng Chen   +8 more
doaj   +1 more source

IgA-dominant postinfectious glomerulonephritis: a case report [PDF]

, 2023
IntroductionAcute postinfectious glomerulonephritis (APIGN) is an immunological glomerular disease that is an important health issue in developing countries.
Werner De Leon-Pérez, David Armas-Eguizabal, Rodolfo Moreno-Alvarado, Jonathan Chávez-Iñiguez, Guillermo Navarro-Blackaller   +4 more
core   +1 more source