Annals of Pediatric Endocrinology & Metabolism


2022 Clinical practice guidelines for central precocious puberty of Korean children and adolescents: Su Jin Kim, Ji Hyun Kim, Yong Hee Hong, In Hyuk Chung, Eun Byoul Lee, Eungu Kang, Jinsup Kim, Aram Yang, Young-Jun Rhie, Eun-Gyong Yoo, Young-Lim Shin, Jin Ho Choi, Soo Young Kim, Jieun Lee; Ann Pediatr Endocrinol Metab. 2023;28(3):168-177. Published online September 19, 2023; DOI: https://doi.org/10.6065/apem.2346168.084
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Myhre syndrome: the first case in Korea: Dongjin Lim, Jae Hyun Kim, Jieun Lee; Ann Pediatr Endocrinol Metab. 2021;26(3):210-214. Published online May 12, 2021; DOI: https://doi.org/10.6065/apem.2040214.107
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Dizygotic twin sisters with normosmic idiopathic hypogonadotropic hypogonadism caused by an FGFR1 gene variant: Jaewon Choe, Jae Hyun Kim, Young Ah Kim, Jieun Lee; Ann Pediatr Endocrinol Metab. 2020;25(3):192-197. Published online July 29, 2020; DOI: https://doi.org/10.6065/apem.1938148.074
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Association between hemoglobin glycation index and cardiometabolic risk factors in Korean pediatric nondiabetic population: Bora Lee, You Jung Heo, Young Ah Lee, Jieun Lee, Jae Hyun Kim, Seong Yong Lee, Choong Ho Shin, Sei Won Yang; Ann Pediatr Endocrinol Metab. 2018;23(4):196-203. Published online December 31, 2018; DOI: https://doi.org/10.6065/apem.2018.23.4.196
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A lack of association between vitamin D-binding protein and 25-hydroxyvitamin D concentrations in pediatric type 1 diabetes without microalbuminuria: Hwa Young Kim, Young Ah Lee, Hae Woon Jung, Min Jeoung Gu, Ji Young Kim, Gyung Min Lee, Jieun Lee, Ju Young Yoon, Sei Won Yang, Choong Ho Shin; Ann Pediatr Endocrinol Metab. 2017;22(4):247-252. Published online December 31, 2017; DOI: https://doi.org/10.6065/apem.2017.22.4.247
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Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion: Aram Yang, Yeon Hee Lee, Soon Young Nam, Yu Ju Jeong, Yechan Kyung, Rimm Huh, Jieun Lee, Younghee Kwun, Sung Yoon Cho, Dong-Kyu Jin; Ann Pediatr Endocrinol Metab. 2015;20(1):40-45. Published online March 31, 2015; DOI: https://doi.org/10.6065/apem.2015.20.1.40
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Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center: Yangho Yoo, Mi Sun Chang, Jieun Lee, Sung Yoon Cho, Sung Won Park, Dong-Kyu Jin, Hyung-Doo Park; Ann Pediatr Endocrinol Metab. 2013;18(3):128-134. Published online September 30, 2013; DOI: https://doi.org/10.6065/apem.2013.18.3.128
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