Annals of Pediatric Endocrinology & Metabolism

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8 Articles


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; Full text PubReader ePub Crossref - TDM PDF


Long-term follow-up on MURCS (Müllerian duct, renal, cervical somite dysplasia) association and a review of the literature: Sun Kim, Yeong Seok Lee, Dong Hyun Kim, Aram Yang, Tack Lee, Seun Deuk Hwang, Dae Gyu Kwon, Ji Eun Lee; Ann Pediatr Endocrinol Metab. 2019;24(3):207-211. Published online September 30, 2019; DOI: https://doi.org/10.6065/apem.2019.24.3.207
Cited By 3; Full text PubReader ePub Crossref - TDM PDF


A case of de novo 18p deletion syndrome with panhypopituitarism: Aram Yang, Jinsup Kim, Sung Yoon Cho, Ji-Eun Lee, Hee-Jin Kim, Dong-Kyu Jin; Ann Pediatr Endocrinol Metab. 2019;24(1):60-63. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.60
Cited By 7; Full text PubReader ePub Crossref - TDM PDF Supplementary Material


A novel de novo mosaic mutation in PHEX in a Korean patient with hypophosphatemic rickets: Misun Yang, Jinsup Kim, Aram Yang, Jahyun Jang, Tae Yeon Jeon, Sung Yoon Cho, Dong-Kyu Jin; Ann Pediatr Endocrinol Metab. 2018;23(4):229-234. Published online December 31, 2018; DOI: https://doi.org/10.6065/apem.2018.23.4.229
Cited By 4; Full text PubReader ePub Crossref - TDM PDF


Etiological trends in male central precocious puberty: Jisun Lee, Jinsup Kim, Aram Yang, Sung Yoon Cho, Dong-Kyu Jin; Ann Pediatr Endocrinol Metab. 2018;23(2):75-80. Published online June 20, 2018; DOI: https://doi.org/10.6065/apem.2018.23.2.75
Cited By 14; Full text PubReader ePub Crossref - TDM PDF


An atypical case of Noonan syndrome with KRAS mutation diagnosed by targeted exome sequencing: Jinsup Kim, Sung Yoon Cho, Aram Yang, Ja-Hyun Jang, Youngbin Choi, Ji-Eun Lee, Dong-Kyu Jin; Ann Pediatr Endocrinol Metab. 2017;22(3):203-207. Published online September 28, 2017; DOI: https://doi.org/10.6065/apem.2017.22.3.203
Cited By 2; Full text PubReader ePub Crossref - TDM PDF


2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis: Eun-Kyung Cho, Jinsup Kim, Aram Yang, Sung Yoon Cho, Dong-Kyu Jin; Ann Pediatr Endocrinol Metab. 2017;22(2):129-132. Published online June 28, 2017; DOI: https://doi.org/10.6065/apem.2017.22.2.129
Cited By 4; Full text PubReader ePub Crossref - TDM PDF


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
Cited By 2; Full text PubReader ePub Crossref - TDM PDF Supplementary Material

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