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Comparison between transient and permanent congenital hypothyroidism on a thyroid function test after re-evaluation
Song Han Lee, Hyun Gyung Lee, Eun Mi Yang, Chan Jong Kim
Ann Pediatr Endocrinol Metab. 2023;28(4):245-250.   Published online December 31, 2023
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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
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Development of delayed thyroid stimulating hormone elevation in small-for-gestational-age infants: is a second screening needed?
Gahyun Lee, So Yun Park, Jae Hyun Park, Seokjin Kang
Ann Pediatr Endocrinol Metab. 2023;28(1):42-48.   Published online June 28, 2022
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Treatment of congenital hypogonadotropic hypogonadism in male patients
Hae Sang Lee, Young Suk Shim, Jin Soon Hwang
Ann Pediatr Endocrinol Metab. 2022;27(3):176-182.   Published online September 30, 2022
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Pasireotide treatment for severe congenital hyperinsulinism due to a homozygous ABCC8 mutation
Christiaan F. Mooij, Carline E. Tacke, Mirjam E. van Albada, Winfried Barthlen, Hennie Bikker, Klaus Mohnike, Matthijs W.N. Oomen, A.S. Paul van Trotsenburg, Nitash Zwaveling-Soonawala
Ann Pediatr Endocrinol Metab. 2021;26(4):278-283.   Published online May 7, 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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Congenital hyperinsulinism: 2 case reports with different rare variants in ABCC8
Julie Mouron-Hryciuk, Sophie Stoppa-Vaucher, Kanetee Busiah, Thérèse Bouthors, Maria Christina Antoniou, Eric Jacot, Klaus Brusgaard, Henrik Thybo Christesen, Khalid Hussain, Andrew Dwyer, Matthias Roth-Kleiner, Michael Hauschild
Ann Pediatr Endocrinol Metab. 2021;26(1):60-65.   Published online August 7, 2020
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An A627V-activating mutation in the thyroid-stimulating hormone receptor gene in familial nonautoimmune hyperthyroidism
Jung Hyun Shin, Go Hun Seo, Seung Hwan Oh, Woo Yeong Chung, Hye Young Kim, Young Mi Kim, Mi Hye Bae, Kyung Hee Park, Min Jung Kwak
Ann Pediatr Endocrinol Metab. 2020;25(4):282-286.   Published online December 31, 2020
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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
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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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Follow-up of infants with congenital hypothyroidism and low total thyroxine/thyroid stimulating hormone on newborn screen
Quinn McCormick, Leslie Pitts, Zachary Hughes
Ann Pediatr Endocrinol Metab. 2019;24(4):237-242.   Published online December 31, 2019
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Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in TG gene
Seung Heo, Ja-Hyun Jang, Jeesuk Yu
Ann Pediatr Endocrinol Metab. 2019;24(3):199-202.   Published online September 30, 2019
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Clinical genetics of defects in thyroid hormone synthesis
Min Jung Kwak
Ann Pediatr Endocrinol Metab. 2018;23(4):169-175.   Published online December 31, 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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Congenital hyperinsulinism: diagnostic and management challenges in a developing country – case report
Cheri Mathews John, Prakash Agarwal, Suriyakumar Govindarajulu, Sandhya Sundaram, Senthil Senniappan
Ann Pediatr Endocrinol Metab. 2017;22(4):272-275.   Published online December 31, 2017
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