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10.1007/s10157-016-1313-5

http://scihub22266oqcxt.onion/10.1007/s10157-016-1313-5
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C5388729!5388729!27422620
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suck abstract from ncbi

pmid27422620      Clin+Exp+Nephrol 2017 ; 21 (2): 193-202
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  • Rituximab for nephrotic syndrome in children #MMPMID27422620
  • Iijima K; Sako M; Nozu K
  • Clin Exp Nephrol 2017[]; 21 (2): 193-202 PMID27422620show ga
  • Idiopathic nephrotic syndrome is the most common chronic glomerular disease in children. At least 20 % of children with this syndrome show frequent relapses and/or steroid dependence during or after immunosuppressive therapies, a condition defined as complicated frequently relapsing/steroid-dependent nephrotic syndrome (FRNS/SDNS). Approximately 1?3 % of children with idiopathic nephrotic syndrome are resistant to steroids and all immunosuppressive agents, a condition defined as refractory steroid-resistant nephrotic syndrome (SRNS); these SRNS children have a high risk of end-stage renal failure. Rituximab, a chimeric anti-CD20 monoclonal antibody, has been shown to be effective for patients with complicated FRNS/SDNS and refractory SRNS. This review describes the recent results of rituximab treatment applied to pediatric nephrotic syndrome, as well as those of our recent study, a multicenter, double-blind, randomized, placebo-controlled trial of rituximab for childhood-onset complicated FRNS/SDNS (RCRNS01). The overall efficacy and safety of rituximab for this disease are discussed.
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