Annals of Pediatric Endocrinology & Metabolism


Bone morbidity in pediatric acute lymphoblastic leukemia: Moon Bae Ahn, Byung-Kyu Suh; Ann Pediatr Endocrinol Metab. 2020;25(1):1-9. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.1
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Updates on bone health in children with gastrointestinal diseases: Hye Ran Yang; Ann Pediatr Endocrinol Metab. 2020;25(1):10-14. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.10
Web of Science 4 Crossref 6; Full text PubReader ePub PDF


Bone health in pediatric patients with neurological disorders: Ara Ko, Juhyun Kong, Furkat Samadov, Akmal Mukhamedov, Young Mi Kim, Yun-Jin Lee, Sang Ook Nam; Ann Pediatr Endocrinol Metab. 2020;25(1):15-23. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.15
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Relationship between final adult height and birth weight after gonadotropin-releasing hormone agonist treatment in girls with central precocious puberty: Ah Young Cho, Su Yeong Ko, Jae Hee Lee, Eun Young Kim; Ann Pediatr Endocrinol Metab. 2020;25(1):24-30. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.24
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Effect of -202 A/C IGFBP-3 polymorphisms on growth responses in children with idiopathic short stature: Hye Ree Kang, Il Tae Hwang, Seung Yang; Ann Pediatr Endocrinol Metab. 2020;25(1):31-37. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.31
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Comparison of proinsulin to C-peptide ratio in children with and without type 1 diabetes and its relation to age: Benjamin R. Ellison, Jeffrey H. Burton, Daniel S. Hsia; Ann Pediatr Endocrinol Metab. 2020;25(1):38-41. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.38
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A homozygous mutation in the insulin gene (INS) causing autosomal recessive neonatal diabetes in Saudi families: Adnan Al Shaikh, Bader Shirah, Somaya Alzelaye; Ann Pediatr Endocrinol Metab. 2020;25(1):42-45. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.42
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Nonclassic congenital lipoid adrenal hyperplasia diagnosed at 17 months in a Korean boy with normal male genitalia: emphasis on pigmentation as a diagnostic clue: Hosun Bae, Min-Sun Kim, Hyojung Park, Ja-Hyun Jang, Jong-Moon Choi, Sae-Mi Lee, Sung Yoon Cho, Dong-Kyu Jin; Ann Pediatr Endocrinol Metab. 2020;25(1):46-51. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.46
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Successful rapid weight reduction and the use of liraglutide for morbid obesity in adolescent Prader-Willi syndrome: Yoo-Mi Kim, Yeoun Joo Lee, Soo Yeon Kim, Chong Kun Cheon, Han Hyuk Lim; Ann Pediatr Endocrinol Metab. 2020;25(1):52-56. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.52
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Persistent goiter with congenital hypothyroidism due to mutation in DUOXA2 gene: So Yoon Jung, Jeongho Lee, Dong Hwan Lee; Ann Pediatr Endocrinol Metab. 2020;25(1):57-62. Published online March 31, 2020; DOI: https://doi.org/10.6065/apem.2020.25.1.57
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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
Web of Science 1 Crossref 2; Full text PubReader ePub PDF

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