Annals of Pediatric Endocrinology & Metabolism

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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; DOI: https://doi.org/10.6065/apem.2244260.130
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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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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; DOI: https://doi.org/10.6065/apem.2244002.001; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2244208.104
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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; DOI: https://doi.org/10.6065/apem.2142010.005
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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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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; DOI: https://doi.org/10.6065/apem.2040042.021
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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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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; 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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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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