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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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Multiple osteoblastomas in a child with Cushing syndrome due to bilateral adrenal micronodular hyperplasias
Hyeoh Won Yu, Won Im Cho, Hye Rim Chung, Keun Hee Choi, Sumi Yun, Hwan Seong Cho, Choong Ho Shin, Sei Won Yang
Ann Pediatr Endocrinol Metab. 2016;21(1):47-50.   Published online March 31, 2016
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Recent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Jin-Ho Choi, Gu-Hwan Kim, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2016;21(1):1-6.   Published online March 31, 2016
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Clinical manifestations of testicular adrenal rest tumor in males with congenital adrenal hyperplasia
Min Kyung Yu, Mo Kyung Jung, Ki Eun Kim, Ah Reum Kwon, Hyun Wook Chae, Duk Hee Kim, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2015;20(3):155-161.   Published online September 30, 2015
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