Results 121 to 130 of about 24,964 (213)

Repository Corticotropin in Treating de novo C3 Glomerulonephritis after Transplantation. [PDF]

Glomerular Dis, 2022
Naseer MS, Singh A, Singh N.
europepmc   +1 more source

Biosynthesis of complement C4 messenger RNA in normal human kidney [PDF]

, 1989
Bevec, Dorian, Felber, E., Feucht, Helmut E., Lang, M., Riethmüller, Gert, Weiss, Elisabeth H., Zwirner, Jörg   +6 more
core   +1 more source

Complete Renal Recovery in Pediatric Patient with C3 Glomerulonephritis: A Case Report. [PDF]

Case Rep Nephrol Dial, 2021
Abdul-Aziz R, Deng R, Liu L, Tarsi S, Waz WR, Wu X.   +5 more
europepmc   +1 more source

Clinical characteristics and short term outcomes of childhood immune complex membranoproliferative glomerulonephritis and C3 glomerulopathy: a single centre retrospective study

BMC Nephrology
Background Membranoproliferative glomerulonephritis, with its immune complex variety and C3 glomerulopathy, is a rare glomerular disease in children. The objective of this study was to determine the clinical features and short-term outcomes in children ...
Irshad Ali Bajeer, Sabeeta Khatri, Pawan Kumar, Seema Hashmi, Mohammed Mubarak, Ali Asghar Lanewala   +5 more
doaj   +1 more source

Renal Disease in Essential Mixed Cryoglobulinaemia: LONG-TERM FOLLOW-UP OF 44 PATIENTS [PDF]

, 2017
The mode of presentation of renal disease in 44 patients with essential mixed cryoglobulinaemia (EMC) was: acute renal failure (two patients), acute nephritic syndrome (six patients), nephrotic syndrome (eight patients), proteinuria and/or haematuria (28
BUSNACHI, G., DE VECCHI, A., DI BELGIOJOSO, G. BARBIANO, IMBASCIATI, E., MIHATSCH, M. J., MONTAGNINO, G., PONTICELLI, C., TARANTINO, A., ZOLLINGER, H. U.   +8 more
core  

C3 glomerulonephritis

Discussion of Clinical Cases, 2015
Hua Chen, Zhi-xia Wang, Jin-li Hao, Chun-yan Ma, Ya-jing Zhang, Wei-guo Jia   +5 more
openaire   +2 more sources

Kartagener Syndrome With Focal Segmental Glomerulosclerosis [PDF]

, 2013
Primary ciliary dyskinesia is characterized by congenital impairment of mucociliary clearance. Kartagener syndrome (KS) is a clinical variant of primary ciliary dyskinesia which is involved in situs inversus associated with chronic respiratory infections.
Doroushi, Behzad, Momeni, Ali, Taheri, Nadia   +2 more
core  

Case Report: Chronic Lymphocytic Leukemia With Recurrent Complement-Mediated Thrombotic Microangiopathy and C3 Glomerulonephritis. [PDF]

Front Med (Lausanne), 2022
Ma T, Wang H, Su T, Wang S.
europepmc   +1 more source

Primary membranoproliferative glomerulonephritis: natural history, pathogenesis, and treatment

Frontiers in Nephrology
Primary membranoproliferative glomerulonephritis (MPGN) is an ultrarare disease characterized by immunofluorescence microscopy as either immune-complex mediated (IC-MPGN) or C3 glomerulopathy (C3), the latter subdivided by electron microscopy to C3 ...
Edward J. Filippone, John L. Farber
doaj   +1 more source

Co-existence of Alport syndrome and C3 glomerulonephritis in a proband with family history. [PDF]

Eur J Med Res, 2021
Ding Y, Tang X, Du Y, Chen H, Yu D, Zhu B, Yuan B.   +6 more
europepmc   +1 more source