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Denosumab use in osteogenesis imperfecta: an update on therapeutic approaches
Fatma Majdoub, Hanene Lassoued Ferjani, Dorra Ben Nessib, Dhia Kaffel, Kaouther Maatallah, Wafa Hamdi
Ann Pediatr Endocrinol Metab. 2023;28(2):98-106.   Published online June 30, 2023
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Genotype-phenotype correlations and long-term efficacy of pamidronate therapy in patients with osteogenesis imperfecta
Yunha Choi, Soojin Hwang, Gu-Hwan Kim, Beom Hee Lee, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2022;27(1):22-29.   Published online January 25, 2022
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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
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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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Pubertal outcomes and sex of rearing of patients with ovotesticular disorder of sex development and mixed gonadal dysgenesis
Yoon Myung Kim, Arum Oh, Kun-Suk Kim, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2019;24(4):231-236.   Published online December 31, 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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Diabetes mellitus due to agenesis of the dorsal pancreas in a patient with heterotaxy syndrome
Jo Eun Jung, Jin Ho Hur, Mo Kyung Jung, Ahreum Kwon, Hyun Wook Chae, Duk Hee Kim, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2017;22(2):125-128.   Published online June 28, 2017
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Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY gene
Jae Yeop Jung, Sohyoung Yang, Eun-Hwan Jeong, Ho-Chang Lee, Yong-Moon Lee, Heon-Seok Han, Kyung Hee Yi
Ann Pediatr Endocrinol Metab. 2015;20(4):226-229.   Published online December 31, 2015
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Turner syndrome presented with tall stature due to overdosage of the SHOX gene
Go Hun Seo, Eungu Kang, Ja Hyang Cho, Beom Hee Lee, Jin-Ho Choi, Gu-Hwan Kim, Eul-Ju Seo, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2015;20(2):110-113.   Published online June 30, 2015
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Hypoparathyroidism, sensorineural deafness, and renal dysgenesis syndrome with a GATA3 mutation
Yong Suk Shim, Woohyeok Choi, Il Tae Hwang, Seung Yang
Ann Pediatr Endocrinol Metab. 2015;20(1):59-63.   Published online March 31, 2015
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Successful Pamidronate Treatment of Osteogenesis Imperfecta Type III Infant with Multiple Fractures.
Ju Hee Yoon, Jong Uk Baek, Eun Jung Shim, Il Tae Hwang
Ann Pediatr Endocrinol Metab. 2012;17(3):194-197.
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The Role of Adipose Tissue Vasculature in Energy Balance.
Hyun Ju Kim, Sang Hyun Choi, Boe Gwun Chun, Dong Hoon Kim
Ann Pediatr Endocrinol Metab. 2011;16(3):139-156.
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Molecular Aspects of Congenital Hypothyroidism.
Jin Ho Choi
Ann Pediatr Endocrinol Metab. 2009;14(2):87-93.
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