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Familial male-limited precocious puberty due to an activating mutation of the LHCGR: a case report and literature review
Jihyun Ha, Yunha Choi,, Mo Kyung Jung, Eun-Gyong Yoo, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2024;29(1):60-66.   Published online February 29, 2024
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Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene
Ji-Hee Yoon, Soojin Hwang, Ja Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2024;29(1):54-59.   Published online February 29, 2024
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Clinical outcomes and genotype-phenotype correlations in patients with complete and partial androgen insensitivity syndromes
Nae-yun Lee, Ja Hye Kim, Ji-Hee Yoon, Soojin Hwang, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2023;28(3):184-192.   Published online February 1, 2023
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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
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Three pediatric patients with primary hyperparathyroidism caused by parathyroid adenoma
Arum Oh, Yena Lee, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2022;27(2):142-147.   Published online May 20, 2021
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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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Diverse etiologies, diagnostic approach, and management of primary adrenal insufficiency in pediatric age
Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2021;26(3):149-157.   Published online September 30, 2021
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Efficacy and safety of intravenous pamidronate infusion for treating osteoporosis in children and adolescents
Ji-Hee Yoon, Yunha Choi, Yena Lee, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2021;26(2):105-111.   Published online June 30, 2021
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Efficacy and safety of parenteral vitamin D therapy in infants and children with vitamin D deficiency caused by intestinal malabsorption
Sae Bit Yu, Yena Lee, Arum Oh, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2020;25(2):112-117.   Published online June 30, 2020
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Clinical, endocrinological, and molecular features of four Korean cases of cytochrome P450 oxidoreductase deficiency
Yena Lee, Jin-Ho Choi, Arum Oh, Gu-Hwan Kim, Sook-Hyun Park, Jung Eun Moon, Cheol Woo Ko, Chong-Kun Cheon, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2020;25(2):97-103.   Published online June 30, 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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Growth hormone therapy in patients with Noonan syndrome
Go Hun Seo, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2018;23(4):176-181.   Published online December 31, 2018
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Hepatopulmonary syndrome caused by hypothalamic obesity and nonalcoholic fatty liver disease after surgery for craniopharyngioma: a case report
Dai Jung, Go Hun Seo, Yoon-Myung Kim, Jin-Ho Choi, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2018;23(1):51-55.   Published online March 22, 2018
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Diabetes mellitus caused by secondary hemochromatosis after multiple blood transfusions in 2 patients with severe aplastic anemia
Hyun Jin Kim, Yoon-Myung Kim, Eungu Kang, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2017;22(1):60-64.   Published online March 31, 2017
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Long-term clinical outcome and the identification of homozygous CYP27B1 gene mutations in a patient with vitamin D hydroxylation-deficient rickets type 1A
Ja Hyang Cho, Eungu Kang, Gu-Hwan Kim, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2016;21(3):169-173.   Published online September 30, 2016
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