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.
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.
KNOW-Ped CKD (KoreaN cohort study for outcomes in patients with pediatric CKD): Design and methods.
Clinical Features and Long-Term outcomes of Patients with Late Steroid Resistant/Sensitive Nephrotic Syndrome: A Single Center Study
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.
Genetic basis of Bartter syndrome in Korea.
Peritoneal Dialysis-related Peritonitis in Children: A Single Center's Experience Over 12 Years
Validity and reliability of the Korean version of the pediatric quality of life ESRD module
A novel mutation and unusual clinical features in a patient with immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome.
Genetic basis of congenital and infantile nephrotic syndromes.
Renal manifestations of patients with MYH9-related disorders.
Clinical Evaluation of Nephrotic Syndrome Manifesting in the First Year of Life
Current Status of Children on Peritoneal Dialysis in Korea : A Cross-Sectional Multicenter Study
산전 초음파로 발견된 선천성 신 요로 기형의 발생률과 임상 결과: 단일 기관 연구.
Nonrefluxing neonatal hydronephrosis and the risk of urinary tract infection
Short-term efficacy of enzyme replacement therapy in Korean patients with Fabry disease.
WT1 and NPHS2 mutations in Korean children with steroid-resistant nephrotic syndrome.
스테로이드 저항성 신증후군에서 cyclosporin 치료반응 및 결과
소아 복막투석 환자에서의 결막과 각막의 석회 침착 1 례
A Case of Posterior Reversible Encephalopathy Syndrome during Cyclosporine Therapy in a Child with Steroid Resistant Nephrotic Syndrome
Clinicopathologic features and prognosis of childhood IgA nephropathy
The clinical manifestations, the short-and long-term outcome of Bartter syndrome
1 year follow-up results of prenatally diagnosed unilateral hydronephrosis according to renal sonographic findings at 1 month of age
Vesicoureteral reflux increases the risk of renal scars: a study of unilateral reflux
신증후군 환아에서 발생한 광범위한 뇌정맥 혈전증 1례
지속적인 주황색 소변을 보인 URAT1 유전자 변이 신성 저요산혈증 1례
연소성 류마티스 관절염의 임상적 고찰
소아에서 스테로이드 반응성 신증후군의 관해기에 발생한 Kimura 병 1례
Growth of long-term survivors after liveing-donor liver transplantation in children
신생아 Batter 증후군 1례
중증 급성 간염으로 발현한 혈구탐식증후군에 관한 연구
소아 IgA 신병증 및 Henoch-Schonlein 신염에서 Fcα 수용체의 유전자 다형성과 mRNA 발현