Annals of Pediatric Endocrinology & Metabolism


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; DOI: https://doi.org/10.6065/apem.2346014.007
Web of Science 3 Crossref 4; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2244152.076
Web of Science 2 Crossref 4; Full text PubReader ePub PDF


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
Web of Science 6 Crossref 7; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2142144.072
Web of Science 4 Crossref 4; Full text PubReader ePub PDF Supplementary Material


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; DOI: https://doi.org/10.6065/apem.1938152.076
Web of Science 6 Crossref 7; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2016.21.3.169
Crossref 8; Full text PubReader ePub PDF


Long-term efficacy of recombinant human growth hormone therapy in short-statured patients with Noonan syndrome: Insook Jeong, Eungu Kang, Ja Hyang Cho, Gu-Hwan Kim, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 2016;21(1):26-30. Published online March 31, 2016; DOI: https://doi.org/10.6065/apem.2016.21.1.26
Crossref 14; Full text PubReader ePub PDF


Endocrine dysfunctions in children with Williams-Beuren syndrome: Yoon-Myung Kim, Ja Hyang Cho, Eungu Kang, Gu-Hwan Kim, Eul-Ju Seo, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 2016;21(1):15-20. Published online March 31, 2016; DOI: https://doi.org/10.6065/apem.2016.21.1.15
Crossref 28; Full text PubReader ePub PDF


Recent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Jin-Ho Choi, Gu-Hwan Kim, Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 2016;21(1):1-6. Published online March 31, 2016; DOI: https://doi.org/10.6065/apem.2016.21.1.1
Crossref 21; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2015.20.2.110
Crossref 6; Full text PubReader ePub PDF


Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience: Sun-Jeong Shin, Yeonah Sul, Ja Hye Kim, Ja Hyang Cho, Gu-Hwan Kim, Jae Hyun Kim, Jin-Ho Choi, Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 2015;20(1):27-33. Published online March 31, 2015; DOI: https://doi.org/10.6065/apem.2015.20.1.27
Crossref 25; Full text PubReader ePub PDF


A novel de novo mutation within PHEX gene in a young girl with hypophosphatemic rickets and review of literature: Chong Kun Cheon, Hoon Sang Lee, Su Yung Kim, Min Jung Kwak, Gu-Hwan Kim, Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 2014;19(1):36-41. Published online March 31, 2014; DOI: https://doi.org/10.6065/apem.2014.19.1.36
Crossref 8; Full text PubReader ePub PDF


p.R182C mutation in Korean twin with congenital lipoid adrenal hyperplasia: Hye Won Park, Byung Ok Kwak, Gu-Hwan Kim, Han-Wook Yoo, Sochung Chung; Ann Pediatr Endocrinol Metab. 2013;18(1):40-43. Published online March 31, 2013; DOI: https://doi.org/10.6065/apem.2013.18.1.40
Crossref 3; Full text PubReader ePub PDF

Search