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  1. A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS
  2. Steroid Regimen for Children with Nephrotic Syndrome Relapse
  3. The Human FSGS-CausingANLNR431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes
  4. AKI in Children Hospitalized with Nephrotic Syndrome