Annals of Pediatric Endocrinology & Metabolism


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; DOI: https://doi.org/10.6065/apem.2040076.038
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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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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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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; DOI: https://doi.org/10.6065/apem.2019.24.4.237
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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; DOI: https://doi.org/10.6065/apem.2019.24.3.199
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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; DOI: https://doi.org/10.6065/apem.2018.23.4.169
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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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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; DOI: https://doi.org/10.6065/apem.2017.22.4.272
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Clinical course of infants with congenital heart disease who developed thyroid dysfunction within 100 days: Hye Jin Lee, Hyeoh Won Yu, Gi Beom Kim, Choong Ho Shin, Sei Won Yang, Young Ah Lee; Ann Pediatr Endocrinol Metab. 2017;22(4):253-258. Published online December 31, 2017; DOI: https://doi.org/10.6065/apem.2017.22.4.253
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Predictors of transient congenital hypothyroidism in children with eutopic thyroid gland: Il Soon Park, Jong Seo Yoon, Cheol Hwan So, Hae Sang Lee, Jin Soon Hwang; Ann Pediatr Endocrinol Metab. 2017;22(2):115-118. Published online June 28, 2017; DOI: https://doi.org/10.6065/apem.2017.22.2.115
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Intellectual development in preschool children with early treated congenital hypothyroidism: Min Kyoung Seo, Jong Seo Yoon, Chul Hwan So, Hae Sang Lee, Jin Soon Hwang; Ann Pediatr Endocrinol Metab. 2017;22(2):102-107. Published online June 28, 2017; DOI: https://doi.org/10.6065/apem.2017.22.2.102
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Severe hyponatremia and repeated intestinal resections for intestinal dysmotility mimicking congenital aganglionic megacolon due to delay in the diagnosis of congenital hypothyroidism: Gonul Buyukyilmaz, Demet Baltu, Tutku Soyer, Murat Tanyıldız, Huseyin Demirbilek; Ann Pediatr Endocrinol Metab. 2016;21(4):230-234. Published online December 31, 2016; DOI: https://doi.org/10.6065/apem.2016.21.4.230
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A baby with congenital hypothyroidism born to a hypothyroid mother who expressed undiagnosed thyroid stimulation blocking antibody: Mock Ryeon Kim, Hye Won Park, Sochung Chung; Ann Pediatr Endocrinol Metab. 2016;21(3):161-163. Published online September 30, 2016; DOI: https://doi.org/10.6065/apem.2016.21.3.161
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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; DOI: https://doi.org/10.6065/apem.2016.21.1.1
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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; DOI: https://doi.org/10.6065/apem.2015.20.3.155
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