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Results 1-10 of 25
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Issue DateTitleAuthor(s)
Oct-2019Reproducibility of the Oxford Classification of IgA nephropathy, impact of biopsy scoring on treatment allocation and clinical relevance of disagreements: evidence from the VALIGA study cohortBellur, S; Roberts, ISD; Troyanov, S; Royal, V; Coppo, R, et al
4-Feb-2019Hyperfunctional complement C3 promotes C5-dependent atypical hemolytic uremic syndrome in miceSmith-Jackson, K; Yang, Y; Denton, H; Pappworth, IY; Cooke, K, et al
Aug-2020Successful simultaneous liver-kidney transplantation for renal failure associated with hereditary complement C3 deficiency.Nayagam, JS; McGrath, S; Montasser, M; Delaney, M; Cairns, TD, et al
Sep-2020Live imaging of monocyte subsets in immune complex-mediated glomerulonephritis reveals distinct phenotypes and effector functions.Turner-Stokes, T; Garcia Diaz, A; Pinheiro, D; Prendecki, M; McAdoo, SP, et al
1-Oct-2014Spleen tyrosine kinase inhibition attenuates autoantibody production and reverses experimental autoimmune GNMcAdoo, SP; Reynolds, J; Bhangal, G; Smith, J; McDaid, JP, et al
9-Sep-2020Autoantibody-dependent amplification of inflammation in SLELou, H; Wojciak-Stothard, B; Ruseva, MM; Cook, HT; Kelleher, P, et al
1-Feb-2021Complement activity is regulated in C3 glomerulopathy by IgG-factor H fusion proteins with and without properdin targeting domainsGilmore, AC; Zhang, Y; Cook, HT; Lavin, DP; Katti, S, et al
30-Mar-2021Gain-of-function factor H–related 5 protein impairs glomerular complement regulation resulting in kidney damageMalik, TH; Gitterman, DP; Lavin, DP; Lomax-Browne, HJ; Hiemeyer, EC, et al
1-Dec-2013C3 glomerulopathy: consensus reportPickering, MC; D'Agati, VD; Nester, CM; Smith, RJ; Haas, M, et al
11-Jun-2007Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domainsPickering, MC; De Jorge, EG; Martinez-Barricarte, R; Recalde, S; Garcia-Layana, A, et al