Lee, M. S., Lee, G. M., Ko, C. W., & Moon, J. E. (2021). Precocious puberty in Korean girls with and without exposure to endocrine-disrupting chemicals in toy slime: a comparative analysis. BMC Endocrine Disorders, 21(1), 1-6.
Lee, M. S., Lee, R., Ko, C. W., & Moon, J. E. (2021). Increase in blood glucose level and incidence of diabetic ketoacidosis in children with type 1 diabetes mellitus in the Daegu-Gyeongbuk area during the coronavirus disease 2019 (COVID-19) pandemic. Yeungnam University Journal of Medicine.
Moon, J. E., Yang, H. Y., Wee, G., ParK, S. H., & Ko, C. W. (2021). A cell function study on calcium regulation of a novel calcium-sensing receptor mutation (p. Tyr825Phe). Annals of Pediatric Endocrinology & Metabolism, 26(1), 24.
Lee, S. Y., Moon, J. E., & Park, S. H. (2021).Longitudinal Changes in Serum Creatinine Levels and Urinary Biomarkers in Late Preterm Infants during the First Postnatal Week: Association with Acute Kidney Injury and Treatment with Aminoglycoside. Children, 8(10), 896.
Jung, J. H., Kim, E. A., Lee, S. Y., Moon, J. E., Lee, E. J., & Park, S. H. . Vitamin D Status and Factors Associated with Vitamin D Deficiency during the First Year of Life in Preterm Infants. Nutrients, 13(6), 2021
Lee, S. J., Moon, J. E., Lee, G. M., Cho, M. H., & Ko, C. W. (2020). An Alport syndrome boy with Van Wyk-Grumbach syndrome induced by prolonged untreated congenital hypothyroidism. Annals of Pediatric Endocrinology & Metabolism, 25(2), 132.
Lee, Y., Choi, J. H., Oh, A., Kim, G. H., Park, S. H., Moon, J. E., ... & Yoo, H. W. (2020). Clinical, endocrinological, and molecular features of four Korean cases of cytochrome P450 oxidoreductase deficiency. Annals of Pediatric Endocrinology & Metabolism, 25(2), 97.
Moon, J. E., & Ko, C. W. (2019). Delayed bone age might accelerate the response to human growth hormone treatment in small for gestational age children with short stature. International journal of endocrinology, 2019.
Moon, J. E., Ko, C. W., Yang, J. D., & Lee, J. S. (2019). Combined surgical and medical treatment in an adolescent with severe gynecomastia due to excessive estradiol secretion: a case report. BMC pediatrics, 19(1), 1-6.
Moon, J. E., Lee, S. J., Park, S. H., Kim, J., Jin, D. K., & Ko, C. W. (2018). De novo a novel variant of CaSR gene in a neonate with congenital hypoparathyroidism. Annals of pediatric endocrinology & metabolism, 23(2), 107.
Moon, J. E., Lee, S. J., & Ko, C. W. (2018). A de novo KMT2D mutation in a girl with Kabuki syndrome associated with endocrine symptoms: a case report. BMC medical genetics, 19(1), 1-4.
Cho, E. M., Moon, J. E., Lee, S. J., & Ko, C. W. (2018). Severe recurrent nocturnal hypoglycemia during chemotherapy with 6-mercaptopurine in a child with acute lymphoblastic leukemia. Annals of Pediatric Endocrinology & Metabolism, 23(4), 1.
Park, S. H., Lee, G. M., Moon, J. E., & Kim, H. M. (2015). Severe vitamin D deficiency in preterm infants: maternal and neonatal clinical features. Korean journal of pediatrics, 58(11), 427.