Annals of Pediatric Endocrinology & Metabolism

Adrenal
Clinical and molecular characteristics of simple virilizing congenital adrenal hyperplasia due to 21-hydroxylase deficiency: insight from a tertiary pediatric center in Vietnam: Khanh Ngoc Nguyen, Giang Thi Kim Dang, Ngoc Thi Bich Can, Dien Minh Tran, Thao Phuong Bui, Mai Nguyen Thi Phuong, Huong Thu Pham, Ngoc Diem Ngo, Dung Chi Vu; Ann Pediatr Endocrinol Metab. 2025;30(6):330-339. Published online May 7, 2025; DOI: https://doi.org/10.6065/apem.2448292.146; Full text PubReader ePub PDF Supplementary Material

Growth & puberty
Cohort profile: Multicenter Networks for Ideal Outcomes of Rare Pediatric Endocrine and Metabolic Diseases in Korea (OUTSPREAD study): Yun Jeong Lee, Chong Kun Cheon, Junghwan Suh, Jung-Eun Moon, Moon Bae Ahn, Seong Hwan Chang, Jieun Lee, Jin Ho Choi, Minsun Kim, Han Hyuk Lim, Jaehyun Kim, Shin-Hye Kim, Hae Sang Lee, Yena Lee, Eungu Kang, Se Young Kim, Yong Hee Hong, Seung Yang, Heon-Seok Han, Sochung Chung, Won Kyoung Cho, Eun Young Kim, Jin Kyung Kim, Kye Shik Shim, Eun-Gyong Yoo, Hae Soon Kim, Aram Yang, Sejin Kim, Hyo-Kyoung Nam, Sung Yoon Cho, Young Ah Lee; Ann Pediatr Endocrinol Metab. 2024;29(6):349-355. Published online December 31, 2024; DOI: https://doi.org/10.6065/apem.2448272.136
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Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome: Ja Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi; Ann Pediatr Endocrinol Metab. 2023;28(2):77-86. Published online June 30, 2023; DOI: https://doi.org/10.6065/apem.2346108.054
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Adrenocortical carcinoma and a sporadic MEN1 mutation in a 3-year-old girl: a case report: Sung Eun Kim, Na Yeong Lee, Won Kyoung Cho, Jisook Yim, Jae Wook Lee, Myungshin Kim, Jae Hee Chung, Min Ho Jung, Byung-Kyu Suh, Moon Bae Ahn; Ann Pediatr Endocrinol Metab. 2022;27(4):315-319. Published online January 17, 2022; DOI: https://doi.org/10.6065/apem.2142100.050
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Diverse etiologies, diagnostic approach, and management of primary adrenal insufficiency in pediatric age: Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 2021;26(3):149-157. Published online September 30, 2021; DOI: https://doi.org/10.6065/apem.2142150.075
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Steroidogenic electron-transfer factors and their diseases: Walter L. Miller; Ann Pediatr Endocrinol Metab. 2021;26(3):138-148. Published online September 30, 2021; DOI: https://doi.org/10.6065/apem.2142154.077
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Identification of a novel point mutation in DAX-1 gene in a patient with adrenal hypoplasia congenita: Han Saem Choi, Ahreum Kwon, Hyun Wook Chae, Junghwan Suh, Kyung Chul Song, Jin-Sung Lee, Ho-Seong Kim; Ann Pediatr Endocrinol Metab. 2021;26(2):126-129. Published online June 30, 2021; DOI: https://doi.org/10.6065/apem.2040088.044
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Two cases of 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 mutation: Hae In Lee, Ahreum Kwon, Jung Hwan Suh, Han Saem Choi, Kyung Chul Song, Hyun Wook Chae, Ho-Seong Kim; Ann Pediatr Endocrinol Metab. 2021;26(1):66-70. Published online March 31, 2021; DOI: https://doi.org/10.6065/apem.2040184.092
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Novel function of adrenocorticotropic hormone in the stimulation of vascular endothelial growth factor release in healthy children and adolescents: a proof-of-concept study: Ryan Heksch, Sasigarn Bowden, Robert Hoffman; Ann Pediatr Endocrinol Metab. 2021;26(1):46-52. Published online February 3, 2021; DOI: https://doi.org/10.6065/apem.2040110.055
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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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A novel compound heterozygous mutation of the AIRE gene in a patient with autoimmune polyendocrine syndrome type 1: Junghwan Suh, Han Saem Choi, Ahreum Kwon, Hyun Wook Chae, Jin-Sung Lee, Ho-Seong Kim; Ann Pediatr Endocrinol Metab. 2019;24(4):248-252. Published online December 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.4.248
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Testicular microlithiasis in a boy with X-linked adrenal hypoplasia congenita: Anastasios Serbis, Vassiliki Regina Tsinopoulou, Konstantina Mouzaki, Eleni P. Kotanidou, Styliani Giza, Assimina Galli-Tsinopoulou; Ann Pediatr Endocrinol Metab. 2018;23(3):162-165. Published online September 28, 2018; DOI: https://doi.org/10.6065/apem.2018.23.3.162
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Compound heterozygosity for a whole gene deletion and p.R124C mutation in CYP21A2 causing nonclassic congenital adrenal hyperplasia: Hamza Nasir, Syed Ibaad Ali, Naeem Haque, Stefan K. Grebe, Salman Kirmani; Ann Pediatr Endocrinol Metab. 2018;23(3):158-161. Published online September 28, 2018; DOI: https://doi.org/10.6065/apem.2018.23.3.158
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Delayed diagnosis of pituitary stalk interruption syndrome with severe recurrent hyponatremia caused by adrenal insufficiency: Kyung Mi Jang, Cheol Woo Ko; Ann Pediatr Endocrinol Metab. 2017;22(3):208-212. Published online September 28, 2017; DOI: https://doi.org/10.6065/apem.2017.22.3.208
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A rare association of central hypothyroidism and adrenal insufficiency in a boy with Williams-Beuren syndrome: Devi Dayal, Dinesh Giri, Senthil Senniappan; Ann Pediatr Endocrinol Metab. 2017;22(1):65-67. Published online March 31, 2017; DOI: https://doi.org/10.6065/apem.2017.22.1.65
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