Results 31 to 40 of about 62,770 (234)

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

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

Comprehensive review of membranoproliferative glomerulonephritis: spotlighting the latest advances in revised classification and treatment [PDF]

Childhood Kidney Diseases, 2023
Membranoproliferative glomerulonephritis (MPGN) is a complex group of renal diseases characterized by a specific pattern of glomerular injury that includes thickening of the capillary wall and mesangial expansion, leading to a heterogeneous group of ...
Jeong Yeon Kim
doaj   +1 more source

Essential mixed cryoglobulinemia type II: case report

Revista de la Facultad de Ciencias Médicas de Córdoba, 2018
The cryoglobulinemic syndrome is produced by precipitating immunoglobulins at low temperatures. Its production is associated with several causes, such as lymphoproliferative disorders, chronic infections and autoimmune disorders. However, the etiology is
Marcos Mazzota, Beatriz Dotto, Viviana Salazar, Mónica Herrero, Ana María Sesín, María Elisa Dionisio de Cabalier, Jorge Mukdsi   +6 more
doaj   +1 more source

Renal Pathologic Findings in TAFRO Syndrome: Is There a Continuum Between Thrombotic Microangiopathy and Membranoproliferative Glomerulonephritis? A Case Report and Literature Review

Frontiers in Immunology, 2019
Background: TAFRO syndrome is a clinical subtype of idiopathic multicentric Castleman disease (iMCD) that is characterized by thrombocytopenia, anasarca, fever and/or elevated serum C-reactive protein, renal dysfunction, and organomegaly.
A. Leurs, V. Gnemmi, A. Lionet, L. Renaud, Jean-Baptiste Gibier, M. Copin, E. Hachulla, P. Hatron, D. Launay, D. Fajgenbaum, L. Terriou   +10 more
semanticscholar   +1 more source

Crescentic membranoproliferative glomerulonephritis in HIV infection; a mini-review with case study [PDF]

Journal of Nephropathology, 2022
HIV-related renal diseases have become more evident and easier to treat due to the prolonged survival of patients with HIV infection on antiretroviral therapy (ART). There are multiple factors involved in the pathogenesis of this entity.
Priti Meena, Vinant Bhargava, Devinder Singh Rana, Anil Kumar Bhalla, Ashwani Gupta, Manish Malik, Pallav Gupta   +6 more
doaj   +1 more source

Validation of distinct pathogenic patterns in a cohort of membranoproliferative glomerulonephritis patients by cluster analysis

Clinical Kidney Journal, 2019
Background A novel data-driven cluster analysis identified distinct pathogenic patterns in C3-glomerulopathies and immune complex-mediated membranoproliferative glomerulonephritis.
Nóra Garam, Z. Prohászka, Á. Szilágyi, C. Aigner, A. Schmidt, M. Gaggl, G. Sunder-Plassmann, D. Bajcsi, J. Brunner, Alexandra Dumfarth, D. Cejka, S. Flaschberger, H. Flögelová, Á. Haris, Ágnes Hartmann, A. Heilos, T. Mueller, K. Rusai, K. Arbeiter, J. Hofer, D. Jakab, Mária Sinkó, E. Szigeti, C. Bereczki, V. Jankó, K. Kelen, G. Reusz, A. Szabó, Nóra Klenk, K. Kóbor, N. Kojc, Maarten Knechtelsdorfer, M. Laganović, A. Lungu, A. Meglič, R. Rus, Tanja Kersnik-Levart, E. Mačionienė, M. Miglinas, A. Pawlowska, T. Stompór, Ľ. Podracká, M. Rudnicki, G. Mayer, R. Ryšavá, J. Reiterová, M. Saraga, T. Seeman, J. Zieg, E. Sladkova, T. Szabó, Andrei Căpitănescu, S. Stancu, M. Tišljar, KRESIMIR Galešić, A. Tislér, Inga Vainumäe, M. Windpessl, T. Zaoral, Galia Zlatanova, D. Csuka   +60 more
semanticscholar   +1 more source

Pathology of C3 Glomerulopathy [PDF]

Childhood Kidney Diseases, 2019
C3 glomerulopathy is a renal disorder involving dysregulation of alternative pathway complement activation. In most instances, a membranoproliferative pattern of glomerular injury with a prevalence of C3 deposition is observed by immunofluorescence ...
Su-Jin Shin, Yoonje Seong, Beom Jin Lim
doaj   +1 more source

Cryoglobulinemic Glomerulonephritis: A Case Report

Siriraj Medical Journal, 2017
Cryoglobulinemic glomerulonephritis (CG) is rare in children. We report a 13-year-old Thai boy who presented with acute nephrotic nephritis syndrome, arthralgia, and purpura. Renal pathology revealed membranoproliferative glomerulonephritis and CG.
Nuntawan Piyaphanee
doaj   +3 more sources

Anaerococcus urinomassiliensis sp. nov., isolated from a urine sample of a 17-year-old boy affected by autoimmune hepatitis and membranoproliferative glomerulonephritis

New Microbes and New Infections, 2016
We report the main characteristics of ‘Anaerococcus urinomassiliensis’ strain FC4T (CSURP2143) that was isolated from a urine sample of a 17-year-old boy affected by autoimmune hepatitis and membranoproliferative glomerulonephritis.
A. Morand, F. Cornu, M. Tsimaratos, J.-C. Lagier, F. Cadoret, P.-E. Fournier, D. Raoult   +6 more
doaj   +1 more source