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- Early prediction of transient versus permanent congenital hypothyroidism: a retrospective cohort study
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Myung Ji Yoo
, Ji-Eun Lee, Eun Young Joo, Jisun Park, Young Ju Suh, Su Jin Kim - Ann Pediatr Endocrinol Metab. 2026;31(1):38-44. Published online February 28, 2026
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- Clinical and molecular characteristics of simple virilizing congenital adrenal hyperplasia due to 21-hydroxylase deficiency: insight from a tertiary pediatric center in Vietnam
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Khanh Ngoc Nguyen
, Giang Thi Kim Dang, Ngoc Thi Bich Can, Dien Minh Tran, Thao Phuong Bui, Mai Nguyen Thi Phuong, Huong Thu Pham, Ngoc Diem Ngo, Dung Chi Vu - Ann Pediatr Endocrinol Metab. 2025;30(6):330-339. Published online May 7, 2025
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Supplementary Material
- Predictive factors of permanent versus transient congenital hypothyroidism: a pragmatic cohort study
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Niki Dermitzaki
, Vasileios Giapros, Marianna Deligeorgopoulou, Vasiliki Rengina Tsinopoulou, Eleni Kotanidou, Maria Baltogianni, Foteini Balomenou, Anastasios Serbis - Ann Pediatr Endocrinol Metab. 2025;30(3):149-156. Published online March 20, 2025
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- Predicting variables associated with diagnostic reevaluation of transient congenital hypothyroidism
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Si-Hwa Gwag, Kyu Hyun Park, Eungu Kang, Hyo-Kyoung Nam, Young-Jun Rhie, Kee-Hyoung Lee
- Ann Pediatr Endocrinol Metab. 2025;30(3):127-134. Published online June 30, 2025
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- Clinical and genetic features of childhood-onset congenital combined pituitary hormone deficiency: a retrospective, single-center cohort study
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Yoonha Lee, Young Ah Lee, Jung Min Ko, Choong Ho Shin, Yun Jeong Lee
- Ann Pediatr Endocrinol Metab. 2024;29(6):379-386. Published online December 31, 2024
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- Age of menarche and final height in patients with permanent congenital hypothyroidism
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Pegah Karimian
, Silva Hovsepian, Tahereh Alinia, Homeyra Raispour, Naghmeh Mirshahzadeh, Mahin Hashemipour - Ann Pediatr Endocrinol Metab. 2024;29(6):371-378. Published online December 31, 2024
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- Cohort profile: Multicenter Networks for Ideal Outcomes of Rare Pediatric Endocrine and Metabolic Diseases in Korea (OUTSPREAD study)
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Yun Jeong Lee, Chong Kun Cheon, Junghwan Suh, Jung-Eun Moon, Moon Bae Ahn, Seong Hwan Chang, Jieun Lee, Jin Ho Choi, Minsun Kim, Han Hyuk Lim, Jaehyun Kim, Shin-Hye Kim, Hae Sang Lee, Yena Lee, Eungu Kang, Se Young Kim, Yong Hee Hong, Seung Yang, Heon-Seok Han, Sochung Chung, Won Kyoung Cho, Eun Young Kim, Jin Kyung Kim, Kye Shik Shim, Eun-Gyong Yoo, Hae Soon Kim, Aram Yang, Sejin Kim, Hyo-Kyoung Nam, Sung Yoon Cho, Young Ah Lee
- Ann Pediatr Endocrinol Metab. 2024;29(6):349-355. Published online December 31, 2024
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- Deciphering the mystery of CHNG3
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Satoshi Narumi
- Ann Pediatr Endocrinol Metab. 2024;29(5):279-283. Published online October 31, 2024
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- Comparison between transient and permanent congenital hypothyroidism on a thyroid function test after re-evaluation
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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
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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?
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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
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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
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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
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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
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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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