Hae I. Cheong
Seoul, Republic of Korea
Last Updated: 09/26/2026
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Found 147 publications
Clinical characteristics and genetic analyses of Korean children with Dent disease.
Journal: Pediatric nephrology (Berlin, Germany)
Published: November 05, 2025
Genotype of PAX2-related disorders correlates with kidney and ocular manifestations.
Journal: European journal of human genetics : EJHG
Published: August 17, 2024
Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tract.
Journal: Pediatric nephrology (Berlin, Germany)
Published: September 11, 2023
Burosumab vs conventional therapy in children with X-linked hypophosphatemia: results of the open-label, phase 3 extension period.
Journal: JBMR plus
Published: August 04, 2023
Genotype-phenotype correlations in children with Gitelman syndrome.
Journal: Clinical and experimental nephrology
Published: July 26, 2023
Corrigendum: Long-term outcome of Bartter syndrome in 54 patients: a multicenter study in Korea.
Journal: Frontiers in medicine
Published: May 19, 2023
Generation of a human induced pluripotent stem cell line from a patient with dent disease.
Journal: Stem cell research
Published: February 17, 2023
Long-term outcome of Bartter syndrome in 54 patients: A multicenter study in Korea.
Journal: Frontiers in medicine
Published: November 16, 2022
Clinical course of post-kidney transplant Schimke immuno-osseous dysplasia.
Journal: Pediatric transplantation
Published: October 27, 2022
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome.
Journal: Nature communications
Published: September 15, 2022
Burosumab vs Phosphate/Active Vitamin D in Pediatric X-Linked Hypophosphatemia: A Subgroup Analysis by Dose Level.
Journal: The Journal of clinical endocrinology and metabolism
Published: June 16, 2022
Last Updated: 09/26/2026