Annals of Pediatric Endocrinology & Metabolism


Turner syndrome due to Xp22.33 deletion combined with 7p22.3 duplication: Ha young Jo, Hyun Ji Jang, Young Mi Kim, Soo-Han Choi, Kyung Hee Park, Hye Won Yoo, Su Jeong Park, Yoon Hee Jo, Min Jung Kwak; Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S14-S16. Published online February 1, 2023; DOI: https://doi.org/10.6065/apem.2244122.061; Full text PubReader ePub PDF


Effect of gonadotropin-releasing hormone agonist treatment on near final height in girls with central precocious puberty and early puberty: Eun Hye Yang, Ha Young Jo, Su Jeong Park, Hye Won Yoo, Soo-Han Choi, Hye-Young Kim, Kyung Hee Park, Young Mi Kim, Min Jung Kwak; Ann Pediatr Endocrinol Metab. 2023;28(1):49-53. Published online March 31, 2023; DOI: https://doi.org/10.6065/apem.2142250.125
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Response to growth hormone according to provocation test results in idiopathic short stature and idiopathic growth hormone deficiency: Ju Young Yoon, Chong Kun Cheon, Jung Hyun Lee, Min Jung Kwak, Hyun-Ji Kim, Ye Jin Kim, Jeong Eun Lee, Woo Yeong Chung, Jeongyun Kim, Jae-Ho Yoo; Ann Pediatr Endocrinol Metab. 2022;27(1):37-43. Published online January 17, 2022; DOI: https://doi.org/10.6065/apem.2142110.055
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An A627V-activating mutation in the thyroid-stimulating hormone receptor gene in familial nonautoimmune hyperthyroidism: Jung Hyun Shin, Go Hun Seo, Seung Hwan Oh, Woo Yeong Chung, Hye Young Kim, Young Mi Kim, Mi Hye Bae, Kyung Hee Park, Min Jung Kwak; Ann Pediatr Endocrinol Metab. 2020;25(4):282-286. Published online December 31, 2020; DOI: https://doi.org/10.6065/apem.2040076.038
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Identification of a novel variant in the PHEX gene using targeted gene panel sequencing in a 24-month-old boy with hypophosphatemic rickets: Ha Young Jo, Jung Hyun Shin, Hye Young Kim, Young Mi Kim, Heirim Lee, Mi Hye Bae, Kyung Hee Park, Ja-Hyun Jang, Min Jung Kwak; Ann Pediatr Endocrinol Metab. 2020;25(1):63-67. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.63
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Clinical genetics of defects in thyroid hormone synthesis: Min Jung Kwak; Ann Pediatr Endocrinol Metab. 2018;23(4):169-175. Published online December 31, 2018; DOI: https://doi.org/10.6065/apem.2018.23.4.169
Web of Science 16 Crossref 16; Full text PubReader ePub PDF


Vitamin D deficiency in children aged 6 to 12 years: single center's experience in Busan: Young Eun Roh, Bo Ryung Kim, Won Bok Choi, Young Mi Kim, Min-Jung Cho, Hye-Young Kim, Kyung Hee Park, Kwang Hoon Kim, Peter Chun, Su Young Kim, Min Jung Kwak; Ann Pediatr Endocrinol Metab. 2016;21(3):149-154. Published online September 30, 2016; DOI: https://doi.org/10.6065/apem.2016.21.3.149
Crossref 18; Full text PubReader ePub PDF


Incidence trends and associated factors of diabetes mellitus in Korean children and adolescents: a retrospective cohort study in Busan and Gyeongnam: Jung Hyun Lee, Yu-Mi Kim, Min Jung Kwak, Su Yung Kim, Hyun-Ji Kim, Chong Kun Cheon, Woo Yeong Chung, Im-Jeong Choi, Su Young Hong, Hee Won Chueh, Jae-Ho Yoo; Ann Pediatr Endocrinol Metab. 2015;20(4):206-212. Published online December 31, 2015; DOI: https://doi.org/10.6065/apem.2015.20.4.206
Crossref 21; Full text PubReader ePub PDF


A Leri-Weill dyschondrosteosis patient confirmed by mutation analysis of SHOX gene: Won Bok Choi, Seung Hyeon Seo, Woo Hyun Yoo, Su Young Kim, Min Jung Kwak; Ann Pediatr Endocrinol Metab. 2015;20(3):162-165. Published online September 30, 2015; DOI: https://doi.org/10.6065/apem.2015.20.3.162
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A novel de novo mutation within PHEX gene in a young girl with hypophosphatemic rickets and review of literature: Chong Kun Cheon, Hoon Sang Lee, Su Yung Kim, Min Jung Kwak, Gu-Hwan Kim, Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 2014;19(1):36-41. Published online March 31, 2014; DOI: https://doi.org/10.6065/apem.2014.19.1.36
Crossref 8; Full text PubReader ePub PDF

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