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X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations

PloS one, 2016-09, Vol.11 (9), p.e0161802-e0161802

2016

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Predicting acute kidney injury in cancer patients using heterogeneous and irregular data

PloS one, 2018-07, Vol.13 (7), p.e0199839-e0199839

2018

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Divergent functions of the Rho GTPases Rac1 and Cdc42 in podocyte injury

Kidney international, 2013-11, Vol.84 (5), p.920-930

2013

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Burden of disease of X-linked hypophosphatemia in Japanese and Korean patients: a cross-sectional survey

Endocrine Journal, 2022, Vol.69(4), pp.373-383

2022

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Clinical Significance of Crescent Formation in IgA Nephropathy – a Multicenter Validation Study

Kidney & blood pressure research, 2019-03, Vol.44 (1), p.22-32

2019

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BK polyomavirus-associated nephropathy

Childhood Kidney Diseases, 2022, 26(1), , pp.11-17

2022

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Hypokalemia as a risk factor for prolonged QT interval and arrhythmia in inherited salt-losing tubulopathy

Childhood Kidney Diseases, 2023, 27(2), , pp.105-110

2023

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Renal artery stenosis presenting as congenital nephrotic syndrome with hyponatremic hypertensive syndrome in a 2-month-old infant: a case report

Childhood Kidney Diseases, 2023, 27(2), , pp.117-120

2023

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Hematuria in children: causes and evaluation

Childhood Kidney Diseases, 2024, 28(2), , pp.66-73

2024

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Genotype–Phenotype Analysis in Pediatric Patients with Distal Renal Tubular Acidosis

Kidney & blood pressure research, 2018-01, Vol.43 (2), p.513-521

2018

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Increasing trend in hypertension prevalence among Korean adolescents from 2007 to 2020

BMC public health, 2024-02, Vol.24 (1), p.617-617, Article 617

2024

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Atypical hemolytic uremic syndrome: Korean pediatric series

Pediatrics international, 2015-06, Vol.57 (3), p.431-438

2015

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Efficacy and safety of losartan in childhood immunoglobulin A nephropathy: a prospective multicenter study

Childhood Kidney Diseases, 2023, 27(2), , pp.97-104

2023

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Life-Threatening Extrarenal Manifestations in an Infant with Atypical Hemolytic Uremic Syndrome Caused by a Complement 3-Gene Mutation

Kidney & blood pressure research, 2019-10, Vol.44 (5), p.1300-1305

2019

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Long-Term Outcomes of Pediatric Renovascular Hypertension

Kidney & blood pressure research, 2017-01, Vol.42 (3), p.617-627

2017

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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

Kidney & blood pressure research, 2017-01, Vol.42 (3), p.406-415

2017

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X-linked hypophosphatemic rickets: from diagnosis to management

Clinical and experimental pediatrics, 2024-01, Vol.67 (1), p.17-25

2024

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Vascular Access Choice, Complications, and Outcomes in Children on Maintenance Hemodialysis: Findings From the International Pediatric Hemodialysis Network (IPHN) Registry

American journal of kidney diseases, 2019-08, Vol.74 (2), p.193-202

2019

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A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants

Kidney international, 2023-05, Vol.103 (5), p.962-972

2023

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COQ6 Mutations in Children With Steroid-Resistant Focal Segmental Glomerulosclerosis and Sensorineural Hearing Loss

American journal of kidney diseases, 2017-07, Vol.70 (1), p.139-144

2017

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Genotype-phenotype correlation of X-linked Alport syndrome observed in both genders: a multicenter study in South Korea

Scientific reports, 2023-04, Vol.13 (1), p.6827-6827, Article 6827

2023

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Investigating the use of finerenone in children with chronic kidney disease and proteinuria: design of the FIONA and open-label extension studies

Trials, 2024-03, Vol.25 (1), p.203-203, Article 203

2024

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Pediatric Kidney Transplantation

Childhood Kidney Diseases, 2021, 25(1), , pp.8-13

2021

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Factors affecting serum concentration of vancomycin in critically ill oliguric pediatric patients receiving continuous venovenous hemodiafiltration

PloS one, 2018-06, Vol.13 (6), p.e0199158-e0199158

2018

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Association of body weight and urinary tract infections during infancy: a nationwide comparative matched cohort study

Childhood Kidney Diseases, 2023, 27(2), , pp.111-116

2023

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X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations

Predicting acute kidney injury in cancer patients using heterogeneous and irregular data

Divergent functions of the Rho GTPases Rac1 and Cdc42 in podocyte injury

Burden of disease of X-linked hypophosphatemia in Japanese and Korean patients: a cross-sectional survey

Clinical Significance of Crescent Formation in IgA Nephropathy – a Multicenter Validation Study

BK polyomavirus-associated nephropathy

Hypokalemia as a risk factor for prolonged QT interval and arrhythmia in inherited salt-losing tubulopathy

Renal artery stenosis presenting as congenital nephrotic syndrome with hyponatremic hypertensive syndrome in a 2-month-old infant: a case report

Hematuria in children: causes and evaluation

Genotype–Phenotype Analysis in Pediatric Patients with Distal Renal Tubular Acidosis

Increasing trend in hypertension prevalence among Korean adolescents from 2007 to 2020

Atypical hemolytic uremic syndrome: Korean pediatric series

Efficacy and safety of losartan in childhood immunoglobulin A nephropathy: a prospective multicenter study

Life-Threatening Extrarenal Manifestations in an Infant with Atypical Hemolytic Uremic Syndrome Caused by a Complement 3-Gene Mutation

Long-Term Outcomes of Pediatric Renovascular Hypertension

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

X-linked hypophosphatemic rickets: from diagnosis to management

Vascular Access Choice, Complications, and Outcomes in Children on Maintenance Hemodialysis: Findings From the International Pediatric Hemodialysis Network (IPHN) Registry

A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants

COQ6 Mutations in Children With Steroid-Resistant Focal Segmental Glomerulosclerosis and Sensorineural Hearing Loss

Genotype-phenotype correlation of X-linked Alport syndrome observed in both genders: a multicenter study in South Korea

Investigating the use of finerenone in children with chronic kidney disease and proteinuria: design of the FIONA and open-label extension studies

Pediatric Kidney Transplantation

Factors affecting serum concentration of vancomycin in critically ill oliguric pediatric patients receiving continuous venovenous hemodiafiltration

Association of body weight and urinary tract infections during infancy: a nationwide comparative matched cohort study

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