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JIMD Reports|January 13, 2023
Pediatric hepatocellular carcinoma associated with Niemann-Pick disease type C: Case report and literature reviewSoojin Hwang, Yunha Choi, Beom Hee Lee, et al.
BMC Pediatrics|March 5, 2021
Etiologic distribution and clinical characteristics of pediatric diabetes in 276 children and adolescents with diabetes at a single academic centerJa Hye Kim, Yena Lee, Yunha Choi, et al.
Endocrine Connections|January 11, 2022
Phenotypic spectrum of patients with mutations in CHD7: clinical implications of endocrinological findingsJa Hye Kim, Yunha Choi, Soojin Hwang, et al.
Annals of Pediatric Endocrinology & Metabolism|October 28, 2014
Long-term follow-up on Cushing disease patient after transsphenoidal surgeryInsook Jeong, Moonyeon Oh, Ja Hye Kim, et al.
Annals of Pediatric Endocrinology & Metabolism|July 8, 2025
Comparison of the effectiveness of recombinant human growth hormone therapy in preterm and full-term children with short stature born small for gestational ageDohyung Kim, Ji-Hee Yoon, Soojin Hwang, et al.
Pediatrics and Neonatology|November 26, 2025
Incidence and multisystem preadolescent complications of Turner syndrome: a nationwide studyJong Ho Cha, Eungu Kang, Jae Yoon Na, et al.
Hormone Research in Paediatrics|July 11, 2015
Identification and Functional Characterization of Two Novel Nonsense Mutations in the β-Subunit of INSR That Cause Severe Insulin Resistance SyndromeJin-Ho Choi, Minji Kang, Ja Hye Kim, et al.
The Journal of Clinical Endocrinology and Metabolism|April 2, 2024
Growth Trajectories of Children Born Preterm and Full-Term With Low Birth Weight to Preschool Ages: A Nationwide StudyJong Ho Cha, Eungu Kang, Jae Yoon Na, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 11, 2017
Long-term Consequences of Congenital Adrenal Hyperplasia due to Classic 21-hydroxylase Deficiency in Adolescents and AdultsJa Hye Kim, Jin-Ho Choi, Eungu Kang, et al.
Annals of Pediatric Endocrinology & Metabolism|March 10, 2024
Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 geneJi-Hee Yoon, Soojin Hwang, Ja Hye Kim, et al.
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