Annals of Pediatric Endocrinology & Metabolism


Thyroid imaging study in children with suspected thyroid dysgenesis: Sangwoo Chun, Young Seok Lee, Jeesuk Yu; Ann Pediatr Endocrinol Metab. 2021;26(1):53-59. Published online March 31, 2021; DOI: https://doi.org/10.6065/apem.2040120.060
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A cell function study on calcium regulation of a novel calcium-sensing receptor mutation (p.Tyr825Phe): Jung Eun Moon, Hee-Young Yang, Gabbine Wee, Suk-Hyun ParK, Cheol Woo Ko; Ann Pediatr Endocrinol Metab. 2021;26(1):24-30. Published online July 30, 2020; DOI: https://doi.org/10.6065/apem.2040022.011
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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; DOI: https://doi.org/10.6065/apem.2040076.038
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A case of primary hyperparathyroidism due to an intrathymic ectopic parathyroid adenoma in a 15-year-old boy: Youngseok Seo, Kyungchul Song, Han Saem Choi, Junghwan Suh, Ahreum Kwon, Hyun Wook Chae, Ho-Seong Kim; Ann Pediatr Endocrinol Metab. 2020;25(3):187-191. Published online July 29, 2020; DOI: https://doi.org/10.6065/apem.1938172.086
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An Alport syndrome boy with Van Wyk-Grumbach syndrome induced by prolonged untreated congenital hypothyroidism: Su-Jeong Lee, Jung-Eun Moon, Gi-Min Lee, Min-Hyun Cho, Cheol Woo Ko; Ann Pediatr Endocrinol Metab. 2020;25(2):132-136. Published online June 30, 2020; DOI: https://doi.org/10.6065/apem.1938074.037
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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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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; Full text PubReader ePub PDF


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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Primary hyperparathyroidism versus familial hypocalciuric hypercalcemia: a challenging diagnostic evaluation in an adolescent female: Mustafa Tosur, Monica E. Lopez, David L. Paul; Ann Pediatr Endocrinol Metab. 2019;24(3):195-198. Published online September 30, 2019; DOI: https://doi.org/10.6065/apem.2019.24.3.195
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Neonatal transient pseudohypoparathyroidism: could it be included among inactivating parathyroid hormone (PTH)/PTH-related protein signalling disorders?: Domenico Umberto De Rose, Alessandro Perri, Francesca Gallini, Francesca Priolo, Eloisa Tiberi, Giovanni Vento, Enrico Zecca; Ann Pediatr Endocrinol Metab. 2019;24(2):129-132. Published online June 30, 2019; DOI: https://doi.org/10.6065/apem.2019.24.2.129
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Thyroid function in girls with central precocious puberty: Geehae Jung, Seok-Bin Oh, Won Young Lee, Hye Ryun Kim, Hyo-Kyoung Nam, Jae Hyun Kim, Young-Jun Rhie, Kee-Hyoung Lee; Ann Pediatr Endocrinol Metab. 2019;24(2):124-128. Published online June 30, 2019; DOI: https://doi.org/10.6065/apem.2019.24.2.124
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Iodine status and characteristics of Korean adolescents and their parents based on urinary iodine concentration: a nationwide cross-sectional study: Yun Chang Choi, Ji In Cheong, Hee Won Chueh, Jae-Ho Yoo; Ann Pediatr Endocrinol Metab. 2019;24(2):108-115. Published online June 30, 2019; DOI: https://doi.org/10.6065/apem.2019.24.2.108
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Screening and management of thyroid dysfunction in preterm infants: Hye Rim Chung; Ann Pediatr Endocrinol Metab. 2019;24(1):15-21. Published online March 31, 2019; DOI: https://doi.org/10.6065/apem.2019.24.1.15
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Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene: Won Kyoung Cho, Moon-Bae Ahn, Woori Jang, Hyojin Chae, Myungshin Kim, Byung-Kyu Suh; Ann Pediatr Endocrinol Metab. 2018;23(4):235-239. Published online December 31, 2018; DOI: https://doi.org/10.6065/apem.2018.23.4.235
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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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