2001. 3 ~ 2005. 8 서울대학교 의과대학원 / 의학박사 1999. 3 ~ 2001 .2 서울대학교 의과대학원 / 의학석사 1992. 3 ~ 1996. 2 서울대학교 의과대학 / 의학사
경력
2014.07 ~ 현재 / 서울대학교 어린이병원 소아청소년 콩팥센터장 2014.07 ~ 현재 / 서울대학교 어린이병원 소아청소년과 소아신장분과 분과장 2017.09 ~ 현재 / 서울대학교 의과대학 교수 2012.03 ~ 2017.08 / 서울대학교 어린이병원 소아청소년과 / 부교수 2008 ~ 2012. 2 / 서울대학교 어린이병원 소아청소년과 / 조교수 2006. 7 ~ 2007. 11 / 미국 미시간대학 신장내과/연구요원 2005. 5 ~ 2006. 2 / 서울대학교병원 장기이식연구소 / 연구교수 2003. 5 ~ 2005. 2 / 미국 하버드 의대 Beth Israel Deaconess 메디컬센터 이식연구소/연구전임의 2001. 3 ~ 2003. 4 / 서울대학교 어린이병원 소아과 소아신장분과/전임의 1997. 3 ~ 2001. 2 / 서울대학교 어린이 병원 소아과 / 전공의 1996 .3 ~ 1997. 3 / 서울대학교병원 / 인턴
논문
Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary Tract
Consensus regarding diagnosis and management of atypical hemolytic uremic syndrome
Clinical Significance of Crescent Formation in IgA Nephropathy - a Multicenter Validation Study
Acute Kidney Injury in Pediatric Cancer Patients
Long-term safety and tolerability of valsartan in children aged 6 to 17 years with hypertension
Anemia and Iron Deficiency in Children with Chronic Kidney Disease (CKD): Data from the Know-Ped CKD Study
Features of Autosomal Recessive Alport Syndrome: A Systematic Review
Association between Serum Matrix Metalloproteinase- (MMP-) 3 Levels and Systemic Lupus Erythematosus: A Meta-analysis
High prevalence of systemic hypertension in pediatric patients with moyamoya disease years after surgical treatment
Acute kidney injury associated with Yersinia pseudotuberculosis infection: Forgotten but not gone
Urological Problems in Patients with Menkes Disease
Reninoma: a rare cause of curable hypertension
A Pediatric Case of a D-Penicillamine Induced ANCA-associated Vasculitis Manifesting a Pulmonary-Renal Syndrome
Mental health and psychosocial adjustment in pediatric chronic kidney disease derived from the KNOW-Ped CKD study
Mycophenolate mofetil for maintenance of remission in children with steroid- and calcineurin inhibitor- dependent nephrotic syndrome: A prospective, randomized multicenter trial
Acute kidney injury predicts all-cause mortality in patients with cancer
Low relapse rate of urinary tract infections from extended-spectrum beta-lactamase-producing bacteria in young children
Post-Transplant Lymphoproliferative Diseases in Pediatric Kidney Allograft Recipients with Epstein-Barr Virus Viremia
Life-Threatening Extrarenal Manifestations in an Infant with Atypical Hemolytic Uremic Syndrome Caused by a Complement 3-Gene Mutation
Primary Hyperoxaluria in Korean Pediatric Patients
Higher Incidence of BK Virus Nephropathy in Pediatric Kidney Allograft Recipients with Alport Syndrome
Vascular Access Choice, Complications, and Outcomes in Children on Maintenance Hemodialysis: Findings From the International Pediatric Hemodialysis Network (IPHN) Registry
Cutaneous Skeletal Hypophosphatemia Syndrome in Association with a Mosaic HRAS Mutation
Predicting acute kidney injury in cancer patients using heterogeneous and irregular data
Genotype-Phenotype Analysis in Pediatric Patients with Distal Renal Tubular Acidosis
Disseminated adenovirus infection in a 10-year-old renal allograft recipient
Factors affecting serum concentration of vancomycin in critically ill oliguric pediatric patients receiving continuous venovenous hemodiafiltration
Kidney Transplantation in Patients with Atypical Hemolytic Uremic Syndrome due to Complement Factor H Deficiency: Impact of Liver Transplantation
A Case of an Ureteropelvic Junction Obstruction Caused by a Crossing Vessel
Acute kidney injury in childhood-onset nephrotic syndrome: Incidence and risk factors in hospitalized patients
A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report
Acute kidney injury and continuous renal replacement therapy in children; what pediatricians need to know
Impact of end-stage renal disease in children on their parents
Efficacy and safety of rituximab in childhood-onset, difficult-to-treat nephrotic syndrome: A multicenter open-label trial in Korea
Measurement of Fluid Status Using Bioimpedance Methods in Korean Pediatric Patients on Hemodialysis
Three cases of Gordon syndrome with dominant KLHL3 mutations
Focal segmental glomerulosclerosis and medullary nephrocalcinosis in children with ADCK4 mutations
COQ6 Mutations in Children With Steroid-Resistant Focal Segmental Glomerulosclerosis and Sensorineural Hearing Loss
NUP107 mutations in children with steroid-resistant nephrotic syndrome
Delayed transplantation may affect intellectual ability in children
Genotype and Phenotype Analysis in Pediatric Patients with Cystinuria
Long-term repeated rituximab treatment for childhood steroid-dependent nephrotic syndrome
A Case of Azathioprine Induced Severe Myelosuppression and Alopecia Totalis in IgA Nephropathy
Markers of disease and steroid responsiveness in paediatric idiopathic nephrotic syndrome: Whole-transcriptome sequencing of peripheral blood mononuclear cells
Loss of podocalyxin causes a novel syndromic type of congenital nephrotic syndrome
Epidemiology of Acute Kidney Injury in Critically Ill Children and Young Adults
Posttransplantation lymphoproliferative disorder after pediatric solid organ transplantation: experiences of 20 years in a single center
A Case of Severe Hypercalcemia Causing Acute Kidney Injury: An Unusual Presentation of Acute Lymphoblastic Leukemia
Long-Term Outcomes of Pediatric Renovascular Hypertension
A 7-year-old girl presenting with a Bartter-like phenotype: Questions
A 7-year-old girl presenting with a Bartter-like phenotype: Answers
Influence of the Method of Definition on the Prevalence of Left-Ventricular Hypertrophy in Children with Chronic Kidney Disease: Data from the Know-Ped CKD Study
The impact of end-stage renal disease in children on their parents
Health-related quality of life of children with pre-dialysis chronic kidney disease
Genotype-phenotype analysis of pediatric patients with WT1 glomerulopathy
Tacrolimus for children with refractory nephrotic syndrome: a one-year prospective, multicenter, and open-label study of Tacrobell(R), a generic formula
The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery
X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations
Hepatorenal fibrocystic diseases in children
A familial case of Blau syndrome caused by a novel NOD2 genetic mutation
Aliskiren Regulates Neonatal Fc Receptor and IgG Metabolism with Attenuation of Anti-GBM Glomerulonephritis in Mice
Targeted exome sequencing resolves allelic and the genetic heterogeneity in the genetic diagnosis of nephronophthisis-related ciliopathy
Recurrence and Treatment after Renal Transplantation in Children with FSGS
KNOW-Ped CKD (KoreaN cohort study for outcomes in patients with pediatric CKD): Design and methods
Bilateral iliac and popliteal arterial thrombosis in a child with focal segmental glomerulosclerosis
A nonsense PAX6 mutation in a family with congenital aniridia
소아 신장이식 환자에서의 면역억제요법
Familial IPEX syndrome: different glomerulopathy in two siblings
Atypical hemolytic uremic syndrome: Korean pediatric series
Nephronophthisis 13: implications of its association with Caroli disease and altered intracellular localization of WDR19 in the kidney
The diagnosis of febrile urinary tract infection in children may be facilitated by urinary biomarkers
Severe Anemia Due to Parvovirus Infection Following Treatment with Rituximab in a Pediatric Kidney Transplant Recipient : Anemia after Treatment of Rituximab in Kidney Recipient Patient
Nephrotic syndrome: what's new, what's hot?
Atypical retinopathy in patients with nephronophthisis type 1: an uncommon ophthalmological finding
Nephronophthisis
Assessment of Worldwide Acute Kidney Injury, Renal Angina and Epidemiology in critically ill children (AWARE): study protocol for a prospective observational study
Initial steroid regimen in idiopathic nephrotic syndrome can be shortened based on duration to first remission
Pharmacodynamic Monitoring of Calcineurin Inhibitor in Pediatric Kidney Transplantation
Different Recurrence Rates Between Pediatric and Adult Renal Transplant for Immunoglobulin A Nephropathy: Predictors of Posttransplant Recurrence
Two siblings with Bardet-Biedl syndrome caused by mutations in BBS10 : the first case identified in Korea
Muscle involvement in Dent disease 2
Recurrence of idiopathic focal segmental glomerulosclerosis after kidney transplantation: experience of a Korean tertiary center
Incidence, risk factors and clinical outcomes for acute kidney injury after aortic arch repair in paediatric patients
X-linked recessive nephrogenic diabetes insipidus: a clinico-genetic study
A case of Sotos syndrome presented with end-stage renal disease due to the posterior urethral valve
Shiga toxin-associated hemolytic uremic syndrome complicated by intestinal perforation in a child with typical hemolytic uremic syndrome
Outcomes of chronic dialysis in Korean children with respect to survival rates and causes of death
Development of antirituximab antibodies in children with nephrotic syndrome
Conversion of twice-daily tacrolimus to once-daily tacrolimus formulation in stable pediatric kidney transplant recipients: pharmacokinetics and efficacy
Intravenous fluid prescription practices among pediatric residents in Korea
Outcome of Antimicrobial Therapy of Pediatric Urinary Tract Infections Caused by Extended-Spectrum beta-Lactamase-Producing Enterobacteriaceae
Leflunomide therapy for BK virus allograft nephropathy after pediatric kidney transplantation
Factors affecting growth and final adult height after pediatric renal transplantation
Active proteases in nephrotic plasma lead to a podocin-dependent phosphorylation of VASP in podocytes via protease activated receptor-1
Prevalence of 25(OH) vitamin D insufficiency and deficiency in pediatric patients on chronic dialysis
Divergent functions of the Rho GTPases Rac1 and Cdc42 in podocyte injury
신증후군 환아에서 Rituximab 사용 후 발생한 기쿠치병 1례
야뇨증의 병인 기전 -항이뇨호르몬, 고칼슘뇨증, 용질성 이뇨
Development of korean rare disease knowledge base
Quality of life in children with end-stage renal disease based on a PedsQL ESRD module
Validity and reliability of the Korean version of the pediatric quality of life ESRD module
Urinary exosomal WT1 in childhood nephrotic syndrome
Genetic basis of Bartter syndrome in Korea
Survival over 2 years of autosomal-recessive renal tubular dysgenesis
GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome
A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene
Renal transplantation in a patient with Bartter syndrome and glomerulosclerosis
Genetic basis of congenital and infantile nephrotic syndromes
Variable renal phenotype in a family with an INF2 mutation
A case of systemic amyloidosis associated with cyclic neutropenia
Transcriptome Profiling of Kidney Tissue from FGS/kist Mice, the Korean Animal Model of Focal Segmental Glomerulosclerosis
Treatment of Recurrent Nephrotic Syndrome after Transplantation
Treatment of steroid-resistant pediatric nephrotic syndrome
Renal manifestations of patients with MYH9-related disorders
Polymorphisms of the MDR1 and MIF genes in children with nephrotic syndrome
Tumour lysis syndrome in children: experience of last decade
Peritonitis in Children Undergoing Peritoneal Dialysis: 10 Years' Experience in a Single Center
A case of Bartter syndrome type I with atypical presentations
Relapsing peritonitis in children who undergo chronic peritoneal dialysis: a prospective study of the international pediatric peritonitis registry
Clinical Characteristics and Associated Anomalies in Children with Solitary Kidney