Results 1 to 10 of about 112,745 (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.
P. Harraka, Tony Wightman, Sarah Akom, Kieran Sandhu, Deb Colville, Andrew Catran, David Langsford, Timothy Pianta, David Barit, Frank Ierino, Alison Skene, Heather Mack, Judy Savige   +12 more
doaj   +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

Metabolic Syndrome in IgA Glomerulonephritis [PDF]

Nephron Extra, 2014
<b><i>Background/Aims:</i></b> Metabolic syndrome (MetS) may have an independent impact on the development of chronic kidney disease. This study examines the prevalence of MetS in subjects with IgA glomerulonephritis (IgAGN) and its impact on disease progression in a retrospective fashion. <b><i>Patients and Methods:&
Kaartinen, Kati, Syrjänen, Jaana, Pörsti, Ilkka, Harmoinen, Aimo, Huhtala, Heini, Mustonen, Jukka   +5 more
openaire   +2 more sources

Hansen's disease with lepra reaction presenting with IgA dominant infection related glomerulonephritis

Indian Journal of Pathology and Microbiology, 2020
Various renal abnormalities in leprosy have been described largely in literature but the occurrence of IgA dominant infection related glomerulonephritis in leprosy with type 2 lepra reaction has not been reported so far. We present here a 60-year-old man
Elayaperumal Indhumathi, Jeyachandran Dhanapriya, Thanigachalam Dineshkumar, Ramanathan Sakthirajan, Natarajan Gopalakrishnan   +4 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

IgA Vasculitis and C3 Glomerulonephritis: One Patient... Various Autoimmune Diseases

Gazeta Médica, 2022
Leucocytoclastic vasculitis refers to a small vessel vasculitis caused by immune complexes, infections and medications. IgA or IgM/IgG immune complexes can be found in direct immunofluorescence studies suggesting specific forms of leucocytoclastic ...
Ana Margarida Pedro Antunes Ferreira Gaudêncio, Ana Catarina Lameiras, Teresa Mendonça   +2 more
doaj   +4 more sources

Anti-glomerular Basement Membrane Disease with Atypical Associations

Saudi Journal of Kidney Diseases and Transplantation, 2021
Anti-glomerular basement membrane (anti-GBM) disease is a systemic autoimmune disorder characterized by circulating immunoglobulin (Ig) G antibodies to carboxy-terminal, noncollagenous 1 domain of type IV collagen of GBM.
Prashant Bharat Malviya, Somashekhar Modigonda, Sanjay Maitra, Swarnalata Gowrishankar   +3 more
doaj   +1 more source

IgA nephropathy in a patient receiving infliximab for generalized pustular psoriasis

BMC Nephrology, 2020
Background IgA nephropathy is the most common glomerulonephritis. Secondary IgA nephropathy complicated with systemic diseases, including psoriasis, is also often reported.
Yuka Segawa, Ryo Ishida, Fuminao Kanehisa, Kunihiro Nakai, Mari Morimoto, Masafumi Seno, Mayuka Nakayama, Tetsuro Kusaba, Norito Katoh, Keiichi Tamagaki   +9 more
doaj   +1 more source

KM55 in the evaluation of IgA containing glomerular diseases

Glomerular Diseases, 2021
Introduction: Mucosal derived galactose deficient IgA is central to the pathogenesis of primary IgA nephropathy. Recent reports suggest similar pathogenesis in Henoch Schonlein purpura and secondary IgA nephropathy.
Rahul Raj, Alok Sharma, Adarsh Barwad, Soumita Bagchi, Sanjay Kumar Agarwal, Arvind Bagga, Amit Kumar Dinda, Geetika Singh   +7 more
doaj   +1 more source

Immune Complex-Mediated Crescentic Glomerulonephritis [PDF]

Journal of Clinical and Diagnostic Research, 2022
Immune complex-mediated Glomerulonephritis (GN) comprises a group of disorders including Immunoglobulin A (IgA) nephropathy, IgA vasculitis, lupus nephritis, infection-related GN {poststreptococcal, Hepatitis C Virus (HCV)}, and fibrillary GN with ...
Dhruvi Reddy, Siva Ranganthan Green, R Hemachandar   +2 more
doaj   +1 more source