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Risk Factors for Renal Scar Formation in Infants With First Episode of Acute Pyelonephritis: A Prospective Clinical Study
Factors associated with reduction of left ventricular mass in children on peritoneal dialysis.
Clinical Characteristics of Transplant-associated Encephalopathy in Children.
Epstein-Barr virus infection in children with renal transplantation: A single-center experience.
Genotype and Phenotype Analysis in Pediatric Patients with Cystinuria.
Genotype-phenotype analysis of pediatric patients with WT1 glomerulopathy.
Health-related quality of life of children with pre-dialysis chronic kidney disease.
The impact of end-stage renal disease in children on their parents.
Clinical Practice Guidelines for the Management of Atypical Hemolytic Uremic Syndrome in Korea.
KNOW-Ped CKD (KoreaN cohort study for outcomes in patients with pediatric CKD): Design and methods.
Targeted exome sequencing resolves allelic and the genetic heterogeneity in the genetic diagnosis of nephronophthisis-related ciliopathy.
Clinical Features and Long-Term outcomes of Patients with Late Steroid Resistant/Sensitive Nephrotic Syndrome: A Single Center Study
Development of monoclonal antibodies against Hantaan virus nucleocapsid protein.
Hepatorenal fibrocystic diseases in children.
Nephronophthisis 13: implications of its association with Caroli disease and altered intracellular localization of WDR19 in the kidney.
Tacrolimus for children with refractory nephrotic syndrome: a one-year prospective, multicenter, and open-label study of Tacrobell®, a generic formula.
Atypical hemolytic uremic syndrome: Korean pediatric series.
Causes and outcomes of asymptomatic gross haematuria in children.
Chronic Kidney Disease-mineral Bone Disorder and Active Vitamin D Analogs for Treating Severe Hyperparathyroidism in Children Receiving Chronic Peritoneal Dialysis
Extrarenal sequential organ failure assessment score as an outcome predictor of critically ill children on continuous renal replacement therapy.
Outcomes of chronic dialysis in Korean children with respect to survival rates and causes of death.
A Case of Autosomal Recessive Pseudohypoaldosteronism Type 1 with a Novel Mutation in the SCNN1A Gene
A Case of Cystinuria with Multiple Renal Stones in an 8-month-old Girl
Intravenous fluid prescription practices among pediatric residents in Korea
Liver transplantation in a child with acute liver failure resulting from drug rash with eosinophilia and systemic symptoms syndrome.
Pediatric Urolithiasis: Our 22-year Experience at a Single Center
Severe hypermagnesemia presenting with abnormal electrocardiographic findings similar to those of hyperkalemia in a child undergoing peritoneal dialysis.
Genetic basis of Bartter syndrome in Korea.
Peritoneal Dialysis-related Peritonitis in Children: A Single Center's Experience Over 12 Years
Quality of life in children with end-stage renal disease based on a PedsQL ESRD module.