H. Cheong

H. Cheong, H. Tsukaguchi, N. Miyake, 2016, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Nephrotic syndrome: what's new, what's hot?

H. Cheong, H. Kang, 2015, Korean journal of pediatrics.

Association of Angiotensin I Converting Enzyme Gene Polymorphism with Reflux Nephropathy in Children

H. Cheong, I. Ha, Yong Choi, 2000, Nephron.

Risk Factors for the Progression of Pediatric Chronic Kidney Disease-A Single Center Study.

H. Cheong, H. Choi, Y. Choi, 2007 .

Glucocorticoid diminishes vascular endothelial growth factor and exacerbates proteinuria in rats with mesangial proliferative glomerulonephritis.

H. Cheong, I. Ha, H. Park, 2002, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Mechanism of Chronic Kidney Disease Progression and Novel Biomarkers: A Metabolomic Analysis of Experimental Glomerulonephritis

H. Cheong, S. Ji, Joo-Youn Cho, 2020, Metabolites.

A nationwide study of mass urine screening tests on Korean school children and implications for chronic kidney disease management

H. Cheong, T. Ha, Su-Young Kim, 2013, Clinical and Experimental Nephrology.

Treatment and long-term outcome in primary distal renal tubular acidosis.

F. Trepiccione, G. Gambaro, Z. Gucev, 2019, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Aliskiren Regulates Neonatal Fc Receptor and IgG Metabolism with Attenuation of Anti-GBM Glomerulonephritis in Mice

H. Cheong, H. Baik, I. Ha, 2016, Nephron.

Renal Syndromic Hearing Loss Is Common in Childhood-onset Chronic Kidney Disease

J. Kim, H. Cheong, I. Ha, 2020, Journal of Korean medical science.

Long-term renal outcome in children with OCRL mutations: retrospective analysis of a large international cohort

Se Jin Park, F. Anglani, J. Moczko, 2016, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Left-ventricular diastolic dysfunction in Korean children with chronic kidney disease: data from the KNOW-Ped CKD study

H. Cheong, Heeyeon Cho, M. Cho, 2020, BMC Nephrology.

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

H. Cheong, Heeyeon Cho, M. Cho, 2017, Kidney and Blood Pressure Research.

Clinical Correlates of Mass Effect in Autosomal Dominant Polycystic Kidney Disease

Hyo Sang Kim, C. Ahn, Y. Pei, 2015, PloS one.

Hyperuricemia and deterioration of renal function in autosomal dominant polycystic kidney disease

C. Ahn, H. Park, A. Kang, 2014, BMC Nephrology.

Genotype and Phenotype Analyses in Pediatric Patients with HNF1B Mutations

J. Kim, H. Cheong, I. Ha, 2020, Journal of clinical medicine.

Association between Serum Matrix Metalloproteinase- (MMP-) 3 Levels and Systemic Lupus Erythematosus: A Meta-analysis

Se Jin Park, H. Cheong, D. S. Kim, 2019, Disease markers.

Systemic Arterial Involvement in Moyamoya Disease

H. Cheong, Yong Choi, 2010 .

Long-Term Outcomes of Pediatric Renovascular Hypertension

H. Cheong, I. Ha, H. Jae, 2017, Kidney and Blood Pressure Research.

Congenital thrombotic thrombocytopenic purpura associated with unilateral moyamoya disease

K. Moon, H. Cheong, J. Chae, 2008, Pediatric Nephrology.

Two siblings with Bardet?Biedl syndrome caused by mutations in BBS10 : the first case identified in Korea

J. Ko, H. Cheong, H. Yu, 2014 .

Identification and Functional Characterization of P159L Mutation in HNF1B in a Family with Maturity-Onset Diabetes of the Young 5 (MODY5)

S. Kwak, K. Park, H. Cheong, 2014, Genomics & informatics.

Clinical and Functional Characterization of URAT1 Variants

Z. Gucev, V. Tasic, H. Cheong, 2011, PloS one.

Urinary exosomal WT1 in childhood nephrotic syndrome

H. Cheong, K. Han, H. Kang, 2012, Pediatric Nephrology.

Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectrum a

R. Hennekam, C. Antignac, A. Kariminejad, 2010 .

Clinical Evaluation of Nephrotic Syndrome Manifesting in the First Year of Life

H. Cheong, Joo Hoon Lee, Y. S. Park, 2009 .

Two Cases of Isolated Diffuse Mesangial Sclerosis with WT1 Mutations

H. Cheong, Y. S. Park, H. Hahn, 2006, Journal of Korean medical science.

A Case of Congenital Nephrotic Syndrome due to Diffuse Mesangial Sclerosis

H. Cheong, D. Jin, Yong Choi, 1998 .

Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicism.

K. Moon, H. Cheong, M. Nagata, 2008, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Peritonitis in Children Undergoing Peritoneal Dialysis: 10 Years' Experience in a Single Center

H. Cheong, I. Ha, K. Han, 2010 .

Dent-2 disease: a mild variant of Lowe syndrome.

V. Tasic, H. Cheong, B. Hoppe, 2009, The Journal of pediatrics.

Urinary Lithiasis in Children : A Single Center Study.

H. Cheong, H. Choi, I. Ha, 2007 .

Transport of Phosphate by Renal Brush Border Membrane Vesicle (BBMV) during Development - Role of the Growth Hormone -

H. Cheong, K. Ko, Yong Choi, 1991 .

Intravenous fluid prescription practices among pediatric residents in Korea

H. Cheong, I. Ha, Yong Choi, 2013, Korean journal of pediatrics.

Familial renal glucosuria: a clinicogenetic study of 23 additional cases

H. Cheong, K. Han, J. Koo, 2012, Pediatric Nephrology.

A Case of Systemic Capillary Leak Syndrome in a Child

H. Cheong, I. Ha, Yong Choi, 2002 .

A Randomized, Double‐Blind, Placebo‐Controlled, Phase 3 Trial Evaluating the Efficacy of Burosumab, an Anti‐FGF23 Antibody, in Adults With X‐Linked Hypophosphatemia: Week 24 Primary Analysis

J. S. San Martin, R. Lachmann, H. Cheong, 2018, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

A Clinical and Molecular Genetic Study of Hypophosphatemic Rickets in Children

H. Cheong, I. Ha, Yong Choi, 2005, Pediatric Research.

Consensus regarding diagnosis and management of atypical hemolytic uremic syndrome

Hee-Jin Kim, Junshik Hong, K. Moon, 2020, The Korean journal of internal medicine.

A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report

N. Matsumoto, H. Cheong, H. Tsukaguchi, 2018, BMC Medical Genetics.

Reduced urinary excretion of thiazide-sensitive Na-Cl cotransporter in Gitelman syndrome: preliminary data.

H. Cheong, Y. Oh, K. Joo, 2007, American journal of kidney diseases : the official journal of the National Kidney Foundation.

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

H. Cheong, Yayoi Nishida, H. Kang, 2021, Endocrine journal.

Efficacy of Burosumab in Adults with X-linked Hypophosphatemia (XLH): A Post Hoc Subgroup Analysis of a Randomized Double-Blind Placebo-Controlled Phase 3 Study

R. Eastell, S. Ralston, M. Brandi, 2022, Calcified Tissue International.

Characteristics of pediatric rhabdomyolysis and the associated risk factors for acute kidney injury: a retrospective multicenter study in Korea

Ji Yeon Song, Ji Yeon Song, H. Cheong, 2021, Kidney research and clinical practice.

Recurrent Hypokalemic Muscle Weakness as an Initial Manifestation of Wilson’s Disease

H. Cheong, T. Kohsaka, I. Ha, 1996 .

Burosumab versus conventional therapy in children with X-linked hypophosphataemia: a randomised, active-controlled, open-label, phase 3 trial

F. Glorieux, H. Cheong, E. Sochett, 2019, The Lancet.

A Pediatric Case of Inflammatory Bowel Disease with Renal Amyloidosis

J. Kim, K. Moon, H. Cheong, 2018, Childhood Kidney Diseases.

A Case of Secondary FSGS due to Chronic Chloride Diarrhea

H. Cheong, K. Yoo, H. Yim, 2016 .

Clinical Practice Guidelines for the Management of Atypical Hemolytic Uremic Syndrome in Korea

H. Cheong, K. Yoo, Heeyeon Cho, 2016, Journal of Korean medical science.

ATP6B1 gene mutations associated with distal renal tubular acidosis and deafness in a child.

H. Cheong, I. Ha, Yong Choi, 2003, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Shiga toxin-associated hemolytic uremic syndrome complicated by intestinal perforation in a child with typical hemolytic uremic syndrome

H. Cheong, H. Choi, I. Ha, 2014, Korean journal of pediatrics.

Burosumab versus conventional therapy in children with X-linked hypophosphataemia: a randomised, active-controlled, open-label, phase 3 trial

F. Glorieux, H. Cheong, E. Sochett, 2019, The Lancet.

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

E. Ars, R. Torra, H. Cheong, 2016 .

Genotype and Phenotype Analysis in X-Linked Hypophosphatemia

H. Cheong, H. Kang, Peong Gang Park, 2021, Frontiers in Pediatrics.

Acute kidney injury associated with Yersinia pseudotuberculosis infection: Forgotten but not gone

H. Cheong, I. Ha, H. Kang, 2019, Kidney research and clinical practice.

Burosumab versus continuation of conventional therapy in children with X-linked hypophosphatemia: a randomised, active-controlled, open-label, phase 3 trial

Farzana, F. Glorieux, H. Cheong, 2020 .

First‐in‐Asian Phase I Study of the Anti‐Fibroblast Growth Factor 23 Monoclonal Antibody, Burosumab: Safety and Pharmacodynamics in Adults With X‐linked Hypophosphatemia

H. Cheong, Hiroyuki Tanaka, K. Ozono, 2018, JBMR plus.

Prevalence of 25(OH) Vitamin D Insufficiency and Deficiency in Pediatric Patients on Chronic Dialysis

H. Cheong, I. Ha, H. Kang, 2013, Peritoneal Dialysis International.

Reduction of plasma homocysteine by folic acid in children with chronic renal failure

H. Cheong, I. Ha, Yong Choi, 2002, Pediatric Nephrology.

Quality of life in children with end-stage renal disease based on a PedsQL ESRD module

H. Cheong, M. Cho, K. Park, 2012, Pediatric Nephrology.

Clinical features of A3243G mitochondrial tRNA mutation

H. Cheong, J. Chae, H. Hwang, 2004, Brain and Development.

Mutational analysis of idiopathic renal hypouricemia in Korea

H. Cheong, I. Ha, T. Igarashi, 2005, Pediatric Nephrology.

Mesenchymal Stem Cells Ameliorate Adriamycin Induced Proteinuric Nephropathy

S. Y. Park, H. Cheong, I. Ha, 2010 .

Efficacy and safety of rituximab in childhood-onset, difficult-to-treat nephrotic syndrome

H. Cheong, Heeyeon Cho, M. Cho, 2018, Medicine.

Nephrogenic Diabetes Insipidus Due to a Novel AVPR2 Mutation

H. Cheong, S. Kalman, M. Taşçılar, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

Severe Acute Kidney Injury with Familial Renal Hypouricemia Confirmed by Genotyping of SLC22A12

H. Cheong, Jung Won Lee, C. Cho, 2020, The Ewha Medical Journal.

Atypical Hemolytic Uremic Syndrome Associated With Complement Factor H Autoantibodies and CFHR1/CFHR3 Deficiency

J. S. Lee, S. Kwak, H. Cheong, 2009, Pediatric Research.

Two Novel Mutations in the Aquaporin 2 Gene in a Girl with Congenital Nephrogenic Diabetes Insipidus

H. Cheong, I. Ha, S. Cho, 2005, Journal of Korean medical science.

Polymorphisms of the NR3C1 gene in Korean children with nephrotic syndrome

H. Cheong, H. Choi, So Hee Lee, 2009 .

Polymorphisms of the NR 3 C 1 gene in Korean children with nephrotic syndrome

H. Cheong, H. Choi, So Hee Lee, 2009 .

Anemia and Iron Deficiency in Children with Chronic Kidney Disease (CKD): Data from the Know-Ped CKD Study

H. Cheong, Heeyeon Cho, M. Cho, 2019, Journal of clinical medicine.

Familial Hearing Loss Associated with mtDNA A1555G Mutation in Korea:1 Pedigree

H. Cheong, Sun O Chang, Seung-ha Oh, 2000 .

Renal manifestations of patients with MYH9-related disorders

K. Moon, H. Cheong, I. Ha, 2011, Pediatric Nephrology.

Influence of VEGF Genetic Polymorphism on Peritoneal Solute Transport in Pediatric Dialysis Patients

H. Cheong, H. Choi, I. Ha, 2010 .

Current Status of Children on Peritoneal Dialysis in Korea : A Cross-Sectional Multicenter Study

H. Cheong, I. Ha, Joo Hoon Lee, 2009 .

Outcomes of Chronic Peritoneal Dialysis by Various Modalities in Korean Children: A Single Center Study.

H. Cheong, H. Choi, I. Ha, 2007 .

Higher Incidence of BK Virus Nephropathy in Pediatric Kidney Allograft Recipients with Alport Syndrome

K. Moon, H. Cheong, S. Min, 2019, Journal of clinical medicine.

Genetic diagnosis of Alport syndrome

H. Cheong, 2019, Korean journal of pediatrics.

Outcomes of chronic dialysis in Korean children with respect to survival rates and causes of death

H. Cheong, M. Cho, I. Ha, 2014, Korean journal of pediatrics.

Genetic tests in children with steroid-resistant nephrotic syndrome

H. Cheong, 2020, Kidney research and clinical practice.

WT1 and NPHS2 mutations in Korean children with steroid-resistant nephrotic syndrome

H. Cheong, H. Choi, I. Ha, 2008, Pediatric Nephrology.

Calpain-mediated Proteolysis of Polycystin-1 C-terminus Induces JAK2 and ERK signal Alterations.

I. So, C. Ahn, H. Park, 2013, Experimental cell research.

Variable renal phenotype in a family with an INF2 mutation

K. Moon, H. Cheong, I. Ha, 2010, Pediatric Nephrology.

Incomplete penetrance of CD46 mutation causing familial atypical hemolytic uremic syndrome

A. Sinha, A. Bagga, H. Cheong, 2015, Pediatric Nephrology.

ADAMTS13 Gene Mutations in Children with Hemolytic Uremic Syndrome

N. Kim, H. Cheong, D. Oh, 2011, Yonsei medical journal.

Peritoneal Protein Loss in Nephrotic Syndrome on Peritoneal Dialysis

H. Cheong, So Hee Lee, I. Ha, 2009 .

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

H. Cheong, June-Dong Park, I. Ha, 2018, PloS one.

Thrombotic microangiopathy: Can liver–kidney transplantation cure aHUS?

H. Cheong, 2009, Nature Reviews Nephrology.

Atypical Hemolytic Uremic Syndrome in a 13-year-old Lao Girl: A Case Report

H. Cheong, Yong Choi, Philavanh Kedsatha, 2019, Childhood Kidney Diseases.

Development of antirituximab antibodies in children with nephrotic syndrome

H. Cheong, H. Choi, I. Ha, 2014, Pediatric Nephrology.

Clinical features of anti-factor H autoantibody-associated hemolytic uremic syndrome.

W. Fridman, A. Bagga, H. Cheong, 2010, Journal of the American Society of Nephrology : JASN.

H. Cheong, I. Ha, Yong Choi, 2004, Pediatric Nephrology.

Autosomal dominant hypocalcemia with Bartter syndrome due to a novel activating mutation of calcium sensing receptor, Y829C

H. Cheong, C. Shin, S. Yang, 2015, Korean journal of pediatrics.

Two Korean Infants with Genetically Confirmed Congenital Nephrotic Syndrome of Finnish Type

K. Moon, H. Cheong, H. Choi, 2009, Journal of Korean medical science.

Variable phenotype of Pierson syndrome

K. Moon, H. Cheong, M. Zenker, 2008, Pediatric Nephrology.

Idiopathic membranous nephropathy in children

K. Moon, H. Cheong, I. Ha, 2006, Pediatric Nephrology.

Leflunomide therapy for BK virus allograft nephropathy after pediatric kidney transplantation

K. Moon, H. Cheong, I. Ha, 2013, Pediatric transplantation.

Long-term repeated rituximab treatment for childhood steroid-dependent nephrotic syndrome

J. Kim, H. Cheong, H. Choi, 2017, Kidney research and clinical practice.

Recurrence of idiopathic focal segmental glomerulosclerosis after kidney transplantation: Experience of a Korean tertiary center

H. Cheong, S. Min, Y. Kim, 2014, Pediatric transplantation.

Nephrotic syndrome in a child after umbilical-cord-blood transplantation

K. Moon, H. Cheong, I. Ha, 2006, Pediatric Nephrology.

Ifosfamide nephrotoxicity in pediatric cancer patients

H. Cheong, I. Ha, H. Shin, 2001, Pediatric Nephrology.

Delayed transplantation may affect intellectual ability in children

H. Cheong, Y. Choi, J. Kim, 2017, Pediatrics international : official journal of the Japan Pediatric Society.

A Case of Wegener's Granulomatosis with Multi-organ Involvement in Childhood.

H. Cheong, I. Ha, Yong Choi, 2007 .

C3 Glomerulonephritis associated with Anti-complement Factor H Autoantibodies in an Adolescent Male: A Case Report

H. Cheong, I. Ha, H. Kang, 2021 .

Primary Hyperoxaluria in Korean Pediatric Patients

Ji Won Lee, H. Cheong, Ji-Hyun Kim, 2019, Childhood Kidney Diseases.

Genotype and Phenotype Analysis in Pediatric Patients with Cystinuria

J. Kim, H. Cheong, I. Ha, 2016, Journal of Korean medical science.

Atypical presentation of distal renal tubular acidosis in two siblings

Z. Gucev, V. Tasic, N. Blau, 2008, Pediatric Nephrology.

Pharmacodynamic Monitoring of Calcineurin Inhibitor in Pediatric Kidney Transplantation

H. Cheong, S. Min, I. Ha, 2015 .

Urinary N-acetyl-β-D glucosaminidase as a surrogate marker for renal function in autosomal dominant polycystic kidney disease: 1 year prospective cohort study

C. Ahn, H. Park, A. Kang, 2012, BMC Nephrology.

Isolation of adenovirus type 7 from the urine of children with acute hemorrhagic cystitis.

H. Cheong, P. Piedra, J. Kasel, 1996, The Pediatric infectious disease journal.

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

K. Moon, M. Seong, S. Park, 2017, American journal of kidney diseases : the official journal of the National Kidney Foundation.

A Case of Azathioprine Induced Severe Myelosuppression and Alopecia Totalis in IgA Nephropathy

H. Cheong, I. Ha, H. Kang, 2017 .

The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase ε.

P. Gipson, Mathieu Lemaire, H. Cheong, 2017, Journal of the American Society of Nephrology : JASN.

Identification of Two Novel BCKDHB Mutations in Korean Siblings with Maple Syrup Urine Disease Showing Mild Clinical Presentation

J. Ko, H. Cheong, C. Shin, 2014 .

Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis

W. Park, H. Cheong, K. Yoo, 2020, Journal of clinical medicine.

Genetics and clinical features of 15 Asian families with steroid-resistant nephrotic syndrome.

M. Muramatsu, H. Cheong, T. Doi, 2006, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

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

H. Cheong, I. Ha, H. Kang, 2015 .

Decreased renal uptake of 99mTc-DMSA in patients with tubular proteinuria

D. Lee, H. Cheong, H. Choi, 2009, Pediatric Nephrology.

Rasburicase improves the outcome of acute kidney injury from typical hemolytic uremic syndrome

J. Kim, H. Cheong, I. Ha, 2020, Pediatric Nephrology.

Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome.

M. Nagasaki, K. Tokunaga, M. Matsuo, 2020, Kidney international.

Low relapse rate of urinary tract infections from extended-spectrum beta-lactamase-producing bacteria in young children

J. Kim, H. Cheong, I. Ha, 2019, Pediatric Nephrology.

Polymorphisms of the MDR1 and MIF genes in children with nephrotic syndrome

H. Cheong, H. Choi, H. Ro, 2011, Pediatric Nephrology.

Outcome of Antimicrobial Therapy of Pediatric Urinary Tract Infections Caused by Extended-Spectrum β-Lactamase-Producing Enterobacteriaceae

H. Cheong, I. Ha, Bongjin Lee, 2013, Infection & chemotherapy.

Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defect

C. Kang, H. Cheong, I. Ha, 2006, Pediatric Nephrology.

Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary Tract

W. Park, H. Cheong, I. Ha, 2020, Journal of clinical medicine.

Tacrolimus for children with refractory nephrotic syndrome: a one-year prospective, multicenter, and open-label study of Tacrobell®, a generic formula

H. Cheong, H. Choi, I. Ha, 2016, World Journal of Pediatrics.

Extraciliary roles of the ciliopathy protein JBTS17 in mitosis and neurogenesis

H. Cheong, Kwangsic Joo, Jeong Ho Lee, 2019, Annals of neurology.

Genotype–phenotype analysis of pediatric patients with WT1 glomerulopathy

H. Cheong, I. Ha, Joo Hoon Lee, 2016, Pediatric Nephrology.

Loss of podocalyxin causes a novel syndromic type of congenital nephrotic syndrome

Murim Choi, J. Ko, H. Cheong, 2017, Experimental & Molecular Medicine.

GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome

H. Cheong, H. Kang, J. Schlondorff, 2012, Pediatric Nephrology.

Genetic basis of congenital and infantile nephrotic syndromes.

K. Moon, H. Cheong, I. Ha, 2011, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Renal manifestations of Dent disease and Lowe syndrome

H. Cheong, H. Choi, I. Ha, 2008, Pediatric Nephrology.

A Case of Hemolytic Uremic Syndrome Complicated by Pneumococcal Necrotizing Pneumonia

H. Cheong, Y. Choe, I. Ha, 2008 .

Phenotype and genotype of Dent’s disease in three Korean boys

H. Cheong, I. Ha, Joo Hoon Lee, 2005, Pediatric Nephrology.

Two Cases of Acute Renal Failure Complicating Paroxysmal Nocturnal Hemoglobinuria in Children

H. Cheong, H. Choi, J. Ryu, 2008 .

Disseminated adenovirus infection in a 10-year-old renal allograft recipient

H. Cheong, J. Ha, I. Ha, 2018, Kidney research and clinical practice.

Impact of end‐stage renal disease in children on their parents

H. Cheong, M. Cho, K. Park, 2018, Nephrology.

C. Ahn, H. Cheong, M. Cho, 2017, Pediatric Nephrology.

Transcriptome Analysis of the Response of Cultured Murine Podocytes to Puromycin Aminonucleoside

H. Cheong, K. Paik, I. Ha, 2010, Nephron Experimental Nephrology.

A Case of Autosomal Recessive Pseudohypoaldosteronism Type 1 with a Novel Mutation in the SCNN1A Gene

H. Cheong, Joo Hoon Lee, Y. S. Park, 2013 .

SOFT syndrome caused by compound heterozygous mutations of POC1A and its skeletal manifestation

Murim Choi, J. Ko, T. Cho, 2016, Journal of Human Genetics.

Bilateral iliac and popliteal arterial thrombosis in a child with focal segmental glomerulosclerosis

H. Cheong, S. Min, I. Ha, 2016, Korean journal of pediatrics.

Dyslipidemia in pediatric CKD patients: results from KNOW-PedCKD (KoreaN cohort study for Outcomes in patients With Pediatric CKD)

H. Cheong, M. Cho, H. Choi, 2020, Pediatric Nephrology.

Pheochromocytoma in Children

H. Cheong, I. Ha, Yong Choi, 1994 .

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations

H. Cheong, H. Choi, I. Ha, 2005, Pediatric Nephrology.

Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome

H. Cheong, Jeonghwan Lee, N. Heo, 2015, Journal of Korean medical science.

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

H. Cheong, H. Choi, Joo Hoon Lee, 2018, Kidney and Blood Pressure Research.

Congenital chloride diarrhea in Korean children: novel mutations and genetic characteristics

H. Cheong, J. Seo, J. Ko, 2013, European Journal of Pediatrics.

Lower albumin level and longer disease duration are risk factors of acute kidney injury in hospitalized children with nephrotic syndrome

J. Kim, H. Cheong, K. Yoo, 2020, Pediatric Nephrology.

Acute Kidney Injury in Pediatric Cancer Patients

H. Yoon, H. Cheong, Hajeong Lee, 2019, The Journal of pediatrics.

Genetic basis of Bartter syndrome in Korea.

H. Cheong, I. Ha, B. Lee, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Renal transplantation in a patient with Bartter syndrome and glomerulosclerosis

K. Moon, H. Cheong, I. Ha, 2011, Korean journal of pediatrics.

A case of Bartter syndrome type I with atypical presentations

H. Cheong, I. Ha, E. Lee, 2010, Korean journal of pediatrics.

Three cases of multicentric carpotarsal osteolysis syndrome: a case series

K. Moon, H. Cheong, Y. Choi, 2018, BMC Medical Genetics.

Development of Korean Rare Disease Knowledge Base

Ju Han Kim, Dokyoon Kim, H. Cheong, 2012, Healthcare informatics research.

Factors affecting growth and final adult height after pediatric renal transplantation.

H. Cheong, I. Ha, H. Jung, 2013, Transplantation proceedings.

KNOW-Ped CKD (KoreaN cohort study for outcomes in patients with pediatric CKD): Design and methods

C. Ahn, K. Oh, H. Cheong, 2016, BMC Nephrology.

Posttransplantation lymphoproliferative disorder after pediatric solid organ transplantation: experiences of 20 years in a single center

H. Cheong, Y. Choi, S. Min, 2017, Korean journal of pediatrics.

Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aalpha chain gene.

P. Hawkins, H. Cheong, I. Ha, 2005, Kidney international.

Clinical Features and Surgical Outcomes of Congenital Cataracts in Patients With Oculocerebrorenal Syndrome

H. Cheong, J. H. Kim, Y. Yu, 2009 .

Clinico-Genetic Study of Nail-Patella Syndrome

T. Cho, H. Cheong, H. Choi, 2009, Journal of Korean medical science.

Postinfectious Glomerulonephritis Associated with Pneumococcus and Influenza A Virus Infection in a Child: a Case Report and Literature Review

H. Cheong, H. Kang, K. Yun, 2019, Pediatric Infection & Vaccine.

Recurrent focal segmental glomerulosclerosis following renal transplantation in Korean pediatric patients

H. Cheong, Yong Choi, I. Jung, 2001, Pediatric transplantation.

A Clinicopathological Study of Rapidly Progressive Glomerulonephritis in Children

H. Cheong, I. Ha, Yong Choi, 2004 .

Hematuria and proteinuria in a mass school urine screening test

H. Cheong, K. Yoo, Kyung Yol Lee, 2005, Pediatric Nephrology.

Pattern of double glomerulopathy in children

K. Moon, H. Cheong, I. Ha, 2007, Pediatric Nephrology.

Nutcracker syndrome in children with gross haematuria: Doppler sonographic evaluation of the left renal vein

H. Cheong, W. Kim, In-One Kim, 2006, Pediatric Radiology.

Markers of disease and steroid responsiveness in paediatric idiopathic nephrotic syndrome: Whole-transcriptome sequencing of peripheral blood mononuclear cells

H. Cheong, I. Ha, H. Seo, 2017, The Journal of international medical research.

Proteinuria in a Boy with Infectious Mononucleosis, C1q Nephropathy, and Dent's Disease

K. Moon, H. Cheong, K. Yun, 2007, Journal of Korean medical science.

Long-term Results of Endoscopic Deflux ® Injection for Vesicoureteral Reflux in Children

H. Cheong, B. Cho, Hwanik Kim, 2015 .

A Case of an Ureteropelvic Junction Obstruction Caused by a Crossing Vessel

H. Cheong, I. Ha, M. Y. Kim, 2018 .

Long-term outcome of Bartter syndrome in 54 patients: A multicenter study in Korea

H. Cheong, E. Bae, Ji Hyun Kim, 2023, Frontiers in Medicine.

Gitelman syndrome combined with complete growth hormone deficiency

H. Cheong, H. Cho, Jeana Hong, 2013, Annals of pediatric endocrinology & metabolism.

Clinical Characteristics and Associated Anomalies in Children with Solitary Kidney

H. Cheong, I. Ha, Yong Choi, 2010 .

A case of a child with non-parasitic chyluria

H. Cheong, D. Jung, J. Koo, 2006 .

Iron Absorption in Patients with Chronic Uremia on Maintenance Hemodialysis and in Healthy Volunteers Measured with a Simple Oral Iron Load Test

H. Cheong, T. Kohsaka, I. Ha, 1996 .

A Pediatric Case of a D-Penicillamine Induced ANCA-associated Vasculitis Manifesting a Pulmonary-Renal Syndrome

J. Kim, K. Moon, H. Cheong, 2019, Journal of Korean medical science.

Post-Transplant Lymphoproliferative Diseases in Pediatric Kidney Allograft Recipients with Epstein-Barr Virus Viremia

H. Cheong, S. Min, J. Ha, 2019, Journal of Korean medical science.

Biallelic Mutations in Nuclear Pore Complex Subunit NUP107 Cause Early-Childhood-Onset Steroid-Resistant Nephrotic Syndrome.

A. Ryo, N. Matsumoto, N. Imamoto, 2015, American journal of human genetics.

A case of Sotos syndrome presented with end-stage renal disease due to the posterior urethral valve

J. Ko, H. Cheong, I. Ha, 2014 .

Long-term outcomes for Asian patients with X-linked hypophosphataemia: rationale and design of the SUNFLOWER longitudinal, observational cohort study

H. Cheong, K. Ozono, S. Fukumoto, 2020, BMJ Open.

Measurement of Fluid Status Using Bioimpedance Methods in Korean Pediatric Patients on Hemodialysis

H. Cheong, H. Choi, I. Ha, 2017, Journal of Korean medical science.

Mental health and psychosocial adjustment in pediatric chronic kidney disease derived from the KNOW-Ped CKD study

H. Cheong, Heeyeon Cho, M. Cho, 2019, Pediatric Nephrology.

Unilateral renal angiodysplasia in a girl with hypertension

H. Cheong, M. Nagata, In-One Kim, 2006, Pediatric Nephrology.

Intravenous Iron Supplementation in Korean Children on Chronic Dialysis

H. Cheong, I. Ha, Yong Choi, 2009 .

Functional Assessment of Fatigue and Other Patient-Reported Outcomes in Patients Enrolled in the Global aHUS Registry

H. Cheong, C. Licht, L. Greenbaum, 2020, Kidney international reports.

Patient-Reported Outcomes from a Randomized, Active-Controlled, Open-Label, Phase 3 Trial of Burosumab Versus Conventional Therapy in Children with X-Linked Hypophosphatemia

F. Glorieux, H. Cheong, Hiroyuki Tanaka, 2021, Calcified Tissue International.

Pseudohypoaldosteronism Type 1 with a Novel Mutation in the NR3C2 Gene: A Case Report

H. Cheong, E. Yang, C. Kim, 2020 .

A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene

H. Cheong, I. Ha, K. Han, 2011, Korean journal of pediatrics.

A case of hemolytic uremic syndrome preceded by intussusception

H. Cheong, Jin Tack Kim, Pil-Sang Jang, 2011, Korean journal of pediatrics.

Antibody depletion by bortezomib through blocking of antigen presentation.

Se Jin Park, H. Cheong, J. Shin, 2013, The New England journal of medicine.

Atypical hemolytic uremic syndrome: Korean pediatric series

W. Park, H. Cheong, K. Yoo, 2015, Pediatrics international : official journal of the Japan Pediatric Society.

Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate

K. Moon, H. Cheong, I. Ha, 2007, Pediatric Nephrology.

A novel mutation of CLCNKB in a Korean patient of mixed phenotype of Bartter-Gitelman syndrome

H. Cheong, Heeyeon Cho, Sang Taek Lee, 2016, Korean journal of pediatrics.

Hospitalizations in dialysis end-stage renal failure patients.

H. Cheong, T. Kohsaka, I. Ha, 1996 .

Efficacy and Safety of Rituximab in Children with Refractory Nephrotic Syndrome; A Multicenter Clinical Trial

H. Cheong, M. Cho, I. Ha, 2014 .

The long-acting C5 inhibitor, ravulizumab, is effective and safe in pediatric patients with atypical hemolytic uremic syndrome naïve to complement inhibitor treatment.

H. Cheong, G. Ariceta, B. Dixon, 2020, Kidney international.

WT1 mutation and steroid-resistant nephrotic syndrome associated with cortical nephrocalcinosis

K. Moon, H. Cheong, So Hee Lee, 2010 .

A Pediatric Case of Long-term Untreated Distal Renal Tubular Acidosis

T. Cho, H. Cheong, H. Shin, 2020 .

Primary Autosomal Recessive Distal Renal Tubular Acidosis Caused by a Common Homozygous SLC4A1 Mutation in Two Lao Families

H. Cheong, E. Yi, Yong Choi, 2018, Journal of Korean medical science.

Failure to thrive and nephrolithiasis in a boy with congenital cyanotic heart anomaly: answers

Z. Gucev, V. Tasic, N. Blau, 2011, Pediatric Nephrology.

Failure to thrive and nephrolithiasis in a boy with congenital cyanotic heart anomaly—questions

Z. Gucev, V. Tasic, N. Blau, 2011, Pediatric Nephrology.

A Case of Antenatal Bartter Syndrome with Sensorineural Deafness

C. Ki, H. Cheong, H. Lee, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Effect of Burosumab Compared With Conventional Therapy on Younger vs Older Children With X-linked Hypophosphatemia

F. Glorieux, H. Cheong, M. Whyte, 2022, The Journal of clinical endocrinology and metabolism.

Muscle involvement in Dent disease 2

H. Cheong, H. Choi, I. Ha, 2014, Pediatric Nephrology.

Attempted treatment of factor H deficiency by liver transplantation

H. Cheong, K. Suh, I. Ha, 2004, Pediatric Nephrology.

Medullary Sponge Kidney Detected in the Pediatric Age

H. Cheong, S. Leem, M. Cho, 2012 .

A single large-scale deletion of mtDNA in a child with recurrent encephalopathy and tubulopathy

H. Cheong, J. Chae, H. Hwang, 2010, Journal of the Neurological Sciences.

KMD: Korean mutation database for genes related to diseases

Jong-Won Kim, H. Cheong, Hyun-Young Park, 2012, Human mutation.

Effects of CoQ10 Replacement Therapy on the Audiological Characteristics of Pediatric Patients with COQ6 Variants

K. Moon, H. Cheong, Seung-ha Oh, 2022, BioMed research international.

Congenital Chloride Diarrhea – Novel Mutation in SLC26A3 Gene

A. Sinha, A. Bagga, H. Cheong, 2016, The Indian Journal of Pediatrics.

Oral Proton Pump Inhibitor for Treatment of Congenital Chloride Diarrhea

Y. Sohn, H. Cheong, J. Jang, 2016 .

Heat Shock Protein 72/73 in Normal and Diseased Kidneys

H. Cheong, T. Kohsaka, I. Ha, 1996 .

Kidney Transplantation in Patients with Atypical Hemolytic Uremic Syndrome due to Complement Factor H Deficiency: Impact of Liver Transplantation

H. Cheong, S. Min, J. Ha, 2017, Journal of Korean medical science.

A novel NOTCH2 mutation identified in a Korean family with Hajdu-Cheney syndrome showing phenotypic diversity.

W. Park, J. Ko, T. Cho, 2015, Annals of clinical and laboratory science.

Survival over 2 years of autosomal-recessive renal tubular dysgenesis

H. Cheong, Su Yeong Kim, E. Kim, 2012, Clinical kidney journal.

Urological Problems in Patients with Menkes Disease

J. Kim, H. Cheong, Y. Choi, 2018, Journal of Korean medical science.

Hypokalemic periodic paralysis; two different genes responsible for similar clinical manifestations

H. Cheong, H. Hwang, Hunmin Kim, 2011, Korean journal of pediatrics.

A Case of Severe Hypercalcemia Causing Acute Kidney Injury: An Unusual Presentation of Acute Lymphoblastic Leukemia

H. Cheong, I. Ha, H. Shin, 2017 .

Two Korean Infants with Genetically Confirmed Congenital Nephrotic Syndrome of Finnish Type

K. Moon, H. Cheong, H. Choi, 2009, Journal of Korean medical science.

Gitelman Syndrome with Normal Serum Magnesium.

H. Cheong, Y. Park, Y. Cheon, 2012 .

From bench to bedside: diagnosis of Gitelman's syndrome -- defect of sodium-chloride cotransporter in renal tissue.

H. Cheong, J. Kim, K. Joo, 2006, Kidney international.

Hypertensive crisis following mRNA COVID-19 vaccination in adolescents: two case reports

H. Cheong, M. Cho, 2022, Childhood Kidney Diseases.

Rapid Resolution of Atypical Hemolytic Uremic Syndrome by Eculizumab Treatment

J. Kim, H. Cheong, I. Ha, 2020 .

Focal segmental glomerulosclerosis and medullary nephrocalcinosis in children with ADCK4 mutations

K. Moon, H. Cheong, M. Nagata, 2017, Pediatric Nephrology.

A familial case of Blau syndrome caused by a novel NOD2 genetic mutation

H. Cheong, I. Ha, H. Kang, 2016, Korean journal of pediatrics.

Atypical retinopathy in patients with nephronophthisis type 1: an uncommon ophthalmological finding

H. Cheong, Y. Yu, I. Ha, 2015, Clinical & experimental ophthalmology.

Intellectual Functioning of Pediatric Patients with Chronic Kidney Disease: Results from the KNOW-Ped CKD

H. Cheong, Heeyeon Cho, M. Cho, 2021, Journal of Korean medical science.

A clinico-genetic study of renal coloboma syndrome in children

H. Cheong, Y. Yu, I. Ha, 2007, Pediatric Nephrology.

Genetic Analysis in Bartter Syndrome from India

H. Cheong, Rachna Sharma, V. Aggarwal, 2014, Indian Journal of Pediatrics.

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

Ji Yeon Song, Kyungmin Kim, H. Cheong, 2023, Scientific reports.

A case of atypical hemolytic uremic syndrome with a transient decrease in complement factor H

H. Cheong, Y. S. Park, H. Hahn, 2006, Pediatric Nephrology.

A 7-year-old girl presenting with a Bartter-like phenotype: Answers

J. Ko, H. Cheong, Sung-Hye Park, 2017, Pediatric Nephrology.

Longterm Follow-up of Autosomal Recessive Polycystic Kidney Disease

H. Cheong, I. Ha, J. Seo, 1998 .

Desmopressin responding female nephrogenic diabetes insipidus: a case report

H. Cheong, K. Pai, Jung Won Lee, 2022, Childhood Kidney Diseases.

Kikuchi-Fujimoto Disease, A Possible Complication of Rituximab Treatment

Ji Won Lee, H. Cheong, I. Ha, 2012 .

A nonsense PAX6 mutation in a family with congenital aniridia

H. Cheong, I. Ha, H. Lee, 2016, Korean journal of pediatrics.

De novo C3 glomerulonephritis in a renal allograft

H. Cheong, B. Kim, S. Song, 2016, Ultrastructural pathology.

Gorham-Stout Syndrome with Focal Segmental Glomerulosclerosis: A Case Report

J. Kim, K. Moon, J. Ko, 2020 .

Urinary Tract Infection Following Voiding Cystourethrography

H. Cheong, H. Choi, J. Ryu, 2008 .