Results 71 to 80 of about 217,483 (203)

Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene.

Molecular Immunology, 2016
C3 glomerulopathy (C3G) is an ultra-rare complement-mediated renal disease characterized histologically by the predominance of C3 deposition within in the glomerulus.
Xue Xiao, C. Ghossein, A. Tortajada, Yuzhou Zhang, N. Meyer, Michael Jones, N. Borsa, C. Nester, Christie P. Thomas, Santiago Rodríquez de Córdoba, Richard J. H. Smith   +10 more
semanticscholar   +1 more source

A case of glomerulonephritis with dominant C3 with organized deposits complicated by non-tuberculous mycobacteria

Human Pathology Reports
We report a case of membranoproliferative glomerulonephritis (MPGN) with dominant C3 and uniquely organized deposits complicated by pulmonary non-tuberculous mycobacterial (NTM) infection.
Masanori Sudo, Chihiro Sakurazawa, Yuichi Sakamaki, Masato Habuka, Asa Ogawa, Yumi Ito, Naofumi Imai, Sayuri Takamura, Satoshi Ito, Akira Shimizu, Shin Goto, Suguru Yamamoto   +11 more
doaj   +1 more source

C4 nephritic factor in patients with immune-complex-mediated membranoproliferative glomerulonephritis and C3-glomerulopathy

Orphanet Journal of Rare Diseases, 2019
Background Acquired or genetic abnormalities of the complement alternative pathway are the primary cause of C3glomerulopathy(C3G) but may occur in immune-complex-mediated membranoproliferative glomerulonephritis (IC-MPGN) as well. Less is known about the
Nóra Garam, Zoltán Prohászka, Ágnes Szilágyi, Christof Aigner, Alice Schmidt, Martina Gaggl, Gere Sunder-Plassmann, Dóra Bajcsi, Jürgen Brunner, Alexandra Dumfarth, Daniel Cejka, Stefan Flaschberger, Hana Flögelova, Ágnes Haris, Ágnes Hartmann, Andreas Heilos, Thomas Mueller, Krisztina Rusai, Klaus Arbeiter, Johannes Hofer, Dániel Jakab, Mária Sinkó, Erika Szigeti, Csaba Bereczki, Viktor Janko, Kata Kelen, György S. Reusz, Attila J. Szabó, Nóra Klenk, Krisztina Kóbor, Nika Kojc, Maarten Knechtelsdorfer, Mario Laganovic, Adrian Catalin Lungu, Anamarija Meglic, Rina Rus, Tanja Kersnik-Levart, Ernesta Macioniene, Marius Miglinas, Anna Pawłowska, Tomasz Stompór, Ludmila Podracka, Michael Rudnicki, Gert Mayer, Romana Rysava, Jana Reiterova, Marijan Saraga, Tomáš Seeman, Jakub Zieg, Eva Sládková, Tamás Szabó, Andrei Capitanescu, Simona Stancu, Miroslav Tisljar, Kresimir Galesic, András Tislér, Inga Vainumäe, Martin Windpessl, Tomas Zaoral, Galia Zlatanova, Dorottya Csuka   +60 more
doaj   +1 more source

C3 Glomerulonephritis: A Rare Case of GN

, 2020
C3 Glomerulonephritis has undergone a recent change in its definition since its consensus review in 2013. Prior to 2013, C3GN would have been classified as a Type 3 Membranoproliferative Glomerulonephritis with the classic pathologic feature of double ...
Shaban, Hesham, Linder, Stanley
core  

Severe active C3 glomerulonephritis triggered by immune complexes and inactivated after eculizumab therapy

Diagnostic Pathology, 2016
BackgroundUnderstanding the role of alternative complement pathway dysregulation in membranoproliferative glomerulonephritis (MPGN) has led to a dramatic shift in its classification into two subgroups: immune complex-mediated MPGN and complement-mediated
T. Kersnik Levart, D. Ferluga, A. Vizjak, J. Mraz, N. Kojc   +4 more
semanticscholar   +1 more source

Testing the Activity of Complement Convertases in Serum/Plasma for Diagnosis of C4NeF-Mediated C3 Glomerulonephritis

Journal of Clinical Immunology, 2016
Autoantibodies termed C3-nephritic factor (C3NeF), which stabilize convertases of the alternative complement pathway, often stimulate autoinflammatory diseases.
A. Blom, F. Corvillo, M. Magda, Grzegorz Stasiłojć, P. Nozal, M. Pérez-Valdivia, Virginia Cabello-Chaves, S. Rodríguez de Córdoba, M. López-Trascasa, M. Okrój   +9 more
semanticscholar   +1 more source

C3 glomerulonephritis with genetically confirmed C3 deficiency in a pediatric patient: a case report [PDF]

Complement component 3 glomerulonephritis (C3GN) is a rare kidney disease characterized by complement dysregulation that results in prominent complement component 3 (C3) deposition in the kidneys. The clinical course of C3GN varies from mild hematuria to
Ji Hong Kim, Jiyoung Oh, Byoung Soo Cho, Jae Il Shin, Seong Heon Kim, Ji-Man Kang, Keum Hwa Lee, Hae Min Kim, Hee Gyung Kang   +8 more
core   +1 more source

Nephrotic syndrome associated with hepatointestinal schistosomiasis Síndrome nefrótica associada à esquistossomose hepatointestinal

Revista do Instituto de Medicina Tropical de São Paulo, 1992
Schistosomal nephropathy has long been related to the hepatosplenic form of schistosomiasis. In the last few years, 24 patients with hepatointestinal schistosomiasis and the nephrotic syndrome were studied.
H. Abensur, I. Nussenzveig, L.B. Saldanha, M.S.C. Petalozzi, M.T. Barros, M. Marcondes, R.T. Barros   +6 more
doaj   +1 more source

Influenza a H1N1 associated acute glomerulonephritis in an adolescent

IDCases, 2020
Influenza virus primarily affects the respiratory system. It rarely causes extrapulmonary complications, with otitis media and febrile seizures being the most common in children.
Garyfallia Syridou, Ioannis Drikos, Artemis Vintila, Antigoni Pegkou, Loukia Zografou, Panagiotis Roungas, Eleni Papa, Dimitris Kyriazopoulos, Olga Savelieva, Eleni Antonopoulou   +9 more
doaj   +1 more source

Evaluating the utility of anti-human IgA, IgG, IgM, Kappa, Lambda-FITC (conjugate) cocktail antibody in transplant renal pathology

Surgical and Experimental Pathology
In this study, we evaluated the utility of polyclonal rabbit anti-human IgA, IgG, IgM, Kappa, Lambda - FITC antibody cocktail (CTA) in identifying immune complex deposits in conjunction with C3 & C1q antibodies in consecutive transplant renal biopsies. A
Shilpi Thakur, Venkatesh Dhanasekaran, Balan Louis Gaspar   +2 more
doaj   +1 more source