Zobrazeno 1 - 10
of 349
pro vyhledávání: '"Glomerular deposits"'
Autor:
Pauline Caillard, Cécile Vigneau, Jean-Michel Halimi, Marc Hazzan, Eric Thervet, Morgane Heitz, Laurent Juillard, Vincent Audard, Marion Rabant, Alexandre Hertig, Jean-François Subra, Vincent Vuiblet, Dominique Guerrot, Mathilde Tamain, Marie Essig, Thierry Lobbedez, Thomas Quemeneur, Mathieu Legendre, Alexandre Ganea, Marie-Noëlle Peraldi, François Vrtovsnik, Maïté Daroux, Raïfah Makdassi, Gabriel Choukroun, Dimitri Titeca-Beauport
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Background and objectivesActivation of the complement system is involved in the pathogenesis of anti-glomerular basement membrane (anti-GBM) disease. Glomerular deposits of complement 3 (C3) are often detected on kidney biopsies. The primary objectiv
Externí odkaz:
https://doaj.org/article/0ad22874263c48ae98270d46d6e02676
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
BMJ Case Rep
Fibrillary glomerulonephritis (FGN) and complement 3 glomerulopathy (C3G) are rare forms of glomerulonephritis with distinct aetiologies. Both FGN and C3G can present with nephritic syndrome. FGN is associated with autoimmune disease, dysproteinaemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cfe102264c9dd8778aa6bb08143e91a
https://pubmed.ncbi.nlm.nih.gov/33602773
https://pubmed.ncbi.nlm.nih.gov/33602773
Autor:
Nicole K. Andeen, Rupali S. Avasare
Publikováno v:
Current Opinion in Nephrology & Hypertension. 30:294-302
Purpose of review Fibrillary glomerulonephritis (FGN) involves ∼1% of native kidney biopsies and is characterized by glomerular deposition of fibrils larger than amyloid (12-24 nm diameter) composed of polyclonal immunoglobulin G (IgG). The recent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3663da0fb5198089ade4f7836fb70ab6
https://doi.org/10.1097/mnh.0000000000000706
https://doi.org/10.1097/mnh.0000000000000706
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Shijian Feng, Hans Adomat, Christopher Nguan, Martin E. Gleave, Sean J. Barbour, Pengcheng Sun, Wanhai Xu, Qiunong Guan, Caigan Du
Publikováno v:
Journal of Inflammation Research. 13:969-983
Background Membranous nephropathy (MN) is a specific entity of glomerulonephritis, and its glomerular inflammation is characterized by the deposition of immune complexes in the glomerular basement membrane and proteinuria. However, the molecular mech
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96009635a360ace7ec9b3ea1f740c879
https://doi.org/10.2147/jir.s285985
https://doi.org/10.2147/jir.s285985
Autor:
Richard K. Sibley, Neiha Arora, Andrew Y. Xiao, Neeraja Kambham, Amanda M Uber, Colin R. Lenihan, John P. Higgins, Zoltan Laszik, Megan L. Troxell, Vivek Charu, Vanderlene L. Kung, Vighnesh Walavalkar, Elizabeth M. Talley, Paul Miller, Cynthia C. Nast
Publikováno v:
Pediatric Nephrology. 36:927-937
Proliferative glomerulonephritis with monoclonal IgG deposits (PGNMID) is a glomerular disease defined by non-organized glomerular deposits of heavy and light chain–restricted immunoglobulin and is rarely reported in children. We characterized a se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08e1a2b98f00b8b1c5a94365153143b7
https://doi.org/10.1007/s00467-020-04763-5
https://doi.org/10.1007/s00467-020-04763-5
Autor:
Satomi Nishikawa, Hiroko Sato, Akane Kashimura, Tetsuya Sakairi, Mao Mizukawa, Hironobu Nishina
Publikováno v:
Journal of Toxicologic Pathology
Hyaline glomerulopathy is a type of glomerular lesion that occurs in aging mice. Spontaneous hyaline glomerulopathy is rare in young mice. Here, we report spontaneous hyaline glomerulopathy in a young adult (15-week-old) ICR mouse. Necropsy revealed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a811a3f8bf835671d97ce5c5b23a6d7
http://europepmc.org/articles/PMC7677629
http://europepmc.org/articles/PMC7677629
Autor:
Wadi N. Suki, Lillian W. Gaber, Faiza N. Khan, Linda W. Moore, Luan D. Truong, Edward A. Graviss, Roberto Barrios, Duc T. Nguyen
Publikováno v:
Kidney International Reports
Introduction Incidental IgA deposits in donor kidneys have unknown sequelae and may predate clinical kidney disease if primed by adverse immunologic or hemodynamic stimuli or may remain dormant. Methods The presence of incidental IgA in post-implanta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b5724618d61ae464df5b762796813dc
http://europepmc.org/articles/PMC7609995
http://europepmc.org/articles/PMC7609995