Annals of Pediatric Endocrinology & Metabolism

Growth & puberty
Utilization of genetic biomarkers for childhood stunting surveillance and early detection in Southeast Asia: a systematic review: Ismail Ismail, Muhammad Nur, Sukma Saini, Alfi Syahar Yakub; Ann Pediatr Endocrinol Metab. 2026;31(2):89-100. Published online April 30, 2026; DOI: https://doi.org/10.6065/apem.2550142.071; Full text PubReader ePub PDF

Genetic
Unraveling PEX6: insights into very-long-chain fatty acid levels and peroxisome biogenesis disorders in pediatric populations: Najmeh Ahangari, Bita Barazandeh Shirvan, Farah Ashrafzadeh, Ehsan Ghayoor Karimiani, Narges Hashemi, Shima Imannezhad, Hashem Lashgari Kalat, Farnoosh Ebrahimzadeh, Javad Akhondian, Mehran Beiraghi Toosi; Ann Pediatr Endocrinol Metab. 2026;31(1):3-10. Published online February 28, 2026; DOI: https://doi.org/10.6065/apem.2550134.067
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AI
ChatGPT: how to use it and the pitfalls/cautions in academia: Jeong-Moo Lee; Ann Pediatr Endocrinol Metab. 2025;30(5):229-241. Published online October 31, 2025; DOI: https://doi.org/10.6065/apem.2550028.014
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Genetic
Phenotypic spectrum and long-term outcomes of patients with 46,XX disorders of sex development: Heeyon Yoon, Dohyung Kim, Ja Hye Kim, Han-Wook Yoo, Jin-Ho Choi; Ann Pediatr Endocrinol Metab. 2025;30(2):77-85. Published online April 30, 2025; DOI: https://doi.org/10.6065/apem.2448122.061
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Deciphering the mystery of CHNG3: Satoshi Narumi; Ann Pediatr Endocrinol Metab. 2024;29(5):279-283. Published online October 31, 2024; DOI: https://doi.org/10.6065/apem.2448186.093
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Long-read next-generation sequencing for molecular diagnosis of pediatric endocrine disorders: Yoko Kuroki, Atsushi Hattori, Keiko Matsubara, Maki Fukami; Ann Pediatr Endocrinol Metab. 2024;29(3):156-160. Published online June 30, 2024; DOI: https://doi.org/10.6065/apem.2448028.014
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Genetic evaluation using next-generation sequencing of children with short stature: a single tertiary-center experience: Su Jin Kim, Eunyoung Joo, Jisun Park, Chang Ahn Seol, Ji-Eun Lee; Ann Pediatr Endocrinol Metab. 2024;29(1):38-45. Published online February 29, 2024; DOI: https://doi.org/10.6065/apem.2346036.018
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A Korean male with Kleefstra syndrome presented with micropenis: Rosie Lee, Mi-seon Lee, Jung Eun Moon; Ann Pediatr Endocrinol Metab. 2023;28(4):308-311. Published online December 31, 2023; DOI: https://doi.org/10.6065/apem.2244174.087
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Denosumab use in osteogenesis imperfecta: an update on therapeutic approaches: Fatma Majdoub, Hanene Lassoued Ferjani, Dorra Ben Nessib, Dhia Kaffel, Kaouther Maatallah, Wafa Hamdi; Ann Pediatr Endocrinol Metab. 2023;28(2):98-106. Published online June 30, 2023; DOI: https://doi.org/10.6065/apem.2346058.029
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Wilson disease diagnosed incidentally by targeted gene panel sequencing in a Korean boy with severe obesity: Minji Im, Ari Song, Jiyeon Kim, Min-Sun Kim, Sae-Mi Lee, Mi Jin Kim, Sung Yoon Cho, Dong-Kyu Jin; Ann Pediatr Endocrinol Metab. 2022;27(3):229-235. Published online October 18, 2021; DOI: https://doi.org/10.6065/apem.2142042.021
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Genetic obesity: an update with emerging therapeutic approaches: Young Bae Sohn; Ann Pediatr Endocrinol Metab. 2022;27(3):169-175. Published online September 30, 2022; DOI: https://doi.org/10.6065/apem.2244188.094
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Demographic and diagnostic markers in new onset pediatric type 1 and type 2 diabetes: differences and overlaps: Teresa Nieto, Beatriz Castillo, Jacobo Nieto, Maria J. Redondo; Ann Pediatr Endocrinol Metab. 2022;27(2):121-125. Published online October 12, 2021; DOI: https://doi.org/10.6065/apem.2142170.085
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Genotype-phenotype correlations and long-term efficacy of pamidronate therapy in patients with osteogenesis imperfecta: Yunha Choi, Soojin Hwang, Gu-Hwan Kim, Beom Hee Lee, Han-Wook Yoo, Jin-Ho Choi; Ann Pediatr Endocrinol Metab. 2022;27(1):22-29. Published online January 25, 2022; DOI: https://doi.org/10.6065/apem.2142144.072
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Balanced assessment of growth disorders using clinical, endocrinological, and genetic approaches: Martin Oswald Savage, Helen Louise Storr; Ann Pediatr Endocrinol Metab. 2021;26(4):218-226. Published online December 31, 2021; DOI: https://doi.org/10.6065/apem.2142208.104
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A pathogenic PHEX variant (c.1483-1G>C) in a Korean patient with X-linked hypophosphatemic rickets: In Hwa Jeong, Jae-Ho Yoo, Namhee Kim; Ann Pediatr Endocrinol Metab. 2021;26(2):130-133. Published online June 30, 2021; DOI: https://doi.org/10.6065/apem.2040186.093
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