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Hormone Research in Paediatrics|November 30, 2018
Variable Clinical Characteristics and Molecular Spectrum of Patients with Syndromes of Reduced Sensitivity to Thyroid Hormone: Genetic Defects in the THRB and SLC16A2 GenesJin-Ho Choi, Ja Hyang Cho, Ja Hye Kim, et al.Annals of Pediatric Endocrinology & Metabolism|January 9, 2026
The effect of education in obese type 2 diabetes adolescents and young adults based on continuous glucose monitoring and smartwatch-derived lifelog dataHyun Ah Woo, Ja Hyang Cho, Kye Shik Shim, et al.Annals of Pediatric Endocrinology & Metabolism|April 23, 2016
Long-term efficacy of recombinant human growth hormone therapy in short-statured patients with Noonan syndromeInsook Jeong, Eungu Kang, Ja Hyang Cho, et al.Journal of Human Genetics|June 24, 2016
Long-term enzyme replacement therapy for Fabry disease: efficacy and unmet needs in cardiac and renal outcomesJa Hye Kim, Beom Hee Lee, Ja Hyang Cho, et al.Journal of Human Genetics|March 20, 2015
Short-term efficacy of N-carbamylglutamate in a patient with N-acetylglutamate synthase deficiencyJa Hye Kim, Yoo-Mi Kim, Beom Hee Lee, et al.Metabolic Brain Disease|May 27, 2019
Phenotypic and molecular spectrum of Korean patients with Lesch-Nyhan syndrome and attenuated clinical variantsJa Hyang Cho, Jin-Ho Choi, Sun Hee Heo, et al.Pediatric Research|June 16, 2026
Levothyroxine use and discontinuation in presumed congenital hypothyroidism: a 10-year nationwide cohort studySeon Young Kim, Hyun Ah Woo, Eun Hye Lee, et al.Annals of Pediatric Endocrinology & Metabolism|July 21, 2015
Turner syndrome presented with tall stature due to overdosage of the SHOX geneGo Hun Seo, Eungu Kang, Ja Hyang Cho, et al.Annals of Pediatric Endocrinology & Metabolism|April 18, 2015
Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experienceSun-Jeong Shin, Yeonah Sul, Ja Hye Kim, et al.Annals of Pediatric Endocrinology & Metabolism|April 23, 2016
Endocrine dysfunctions in children with Williams-Beuren syndromeYoon-Myung Kim, Ja Hyang Cho, Eungu Kang, et al.Pageof 3