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Stem Cell Research|February 28, 2025
Human induced pluripotent stem cell line (PNUSCRi006-A) derived from a patient with Sanfilippo syndrome type A exhibiting a mutation in SGSH geneNayeon Lee, Haneul Noh, Chong Kun Cheon
Kidney Research and Clinical Practice|December 19, 2021
Fabry nephropathy before and after enzyme replacement therapy: important role of renal biopsy in patients with Fabry diseaseIl Young Kim, Hyun Jung Lee, Chong Kun Cheon
Yonsei Medical Journal|December 17, 2014
The first Korean case of HDR syndrome confirmed by clinical and molecular investigationChong Kun Cheon, Gu Hwan Kim, Han Wook Yoo
Korean Journal of Pediatrics|August 1, 2014
Two adolescent patients with coexistent Graves' disease and Moyamoya disease in KoreaChong Kun Cheon, Su Yung Kim, Jae-Ho Yoo
International Journal of Molecular Sciences|October 2, 2020
Functional Characterization of Gomisin N in High-Fat-Induced <i>Drosophila</i> Obesity ModelsJoo Young Lee, Ji Hye Lee, Chong Kun Cheon
Annals of Pediatric Endocrinology & Metabolism|January 18, 2022
The first case of novel variants of the FSHR mutation causing primary amenorrhea in 2 siblings in KoreaSukdong Yoo, Ju Young Yoon, Changwon Keum, et al.
Orphanet Journal of Rare Diseases|July 4, 2021
Clinical relevance of targeted exome sequencing in patients with rare syndromic short statureGilyazetdinov Kamil, Ju Young Yoon, Sukdong Yoo, et al.
Child Health Nursing Research|February 1, 2024
Healthcare coaching program for youth with type 1 diabetes in South Korea: a pilot studyDae Eun Lee, Haejung Lee, Chong Kun Cheon, et al.
Korean Journal of Pediatrics|January 6, 2018
The First Korean case of combined oxidative phosphorylation deficiency-17 diagnosed by clinical and molecular investigationYoung A Kim, Yoo-Mi Kim, Yun-Jin Lee, et al.
Pediatric Neurology|July 12, 2014
OTC gene in ornithine transcarbamylase deficiency: clinical course and mutational spectrum in seven Korean patientsJung Hyun Lee, Gu-Hwan Kim, Han-Wook Yoo, et al.
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