Annals of Pediatric Endocrinology & Metabolism

Search: Ann Pediatr Endocrinol Metab Search

CLOSE

Author Index

Page Path

HOME
BROWSE ARTICLES
Author Index

30 Articles


Long-term endocrine sequelae after hematopoietic stem cell transplantation in children and adolescents: Soojin Hwang, Yena Lee, Ji-Hee Yoon, Ja Hye Kim, Hyery Kim, Kyung-Nam Koh, Ho Joon Im, Han-Wook Yoo, Jin-Ho Choi; Ann Pediatr Endocrinol Metab. 2024;29(2):109-118. Published online January 24, 2024; DOI: https://doi.org/10.6065/apem.2346046.023
Crossref 1; Full text PubReader ePub PDF


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; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2346042.021; 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; 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 2 Crossref 3; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2142006.003
Web of Science 2 Crossref 5; 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 2 Crossref 2; Full text PubReader ePub PDF Supplementary Material


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; DOI: https://doi.org/10.6065/apem.2142150.075
Web of Science 6 Crossref 7; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2040150.075
Web of Science 6 Crossref 7; Full text PubReader ePub PDF


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


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; DOI: https://doi.org/10.6065/apem.1938142.071
Web of Science 4 Crossref 4; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2019.24.4.231
Web of Science 6 Crossref 9; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2018.23.4.176
Web of Science 16 Crossref 19; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2018.23.1.51
Web of Science 4 Crossref 5; Full text PubReader ePub PDF


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; DOI: https://doi.org/10.6065/apem.2017.22.1.60
Crossref 1; Full text PubReader ePub PDF


Etiology and therapeutic outcomes of children with gonadotropin-independent precocious puberty: Eungu Kang, Ja Hyang Cho, Jin-Ho Choi, Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 2016;21(3):136-142. Published online September 30, 2016; DOI: https://doi.org/10.6065/apem.2016.21.3.136
Crossref 4; 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 4; 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 18; 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 24; 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


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 5; 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 24; Full text PubReader ePub PDF


Long-term follow-up on Cushing disease patient after transsphenoidal surgery: Insook Jeong, Moonyeon Oh, Ja Hye Kim, Ja Hyang Cho, Jin-Ho Choi, Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 2014;19(3):164-168. Published online September 30, 2014; DOI: https://doi.org/10.6065/apem.2014.19.3.164
Crossref 2; Full text PubReader ePub PDF


Efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency: Ja Hye Kim, Ja Hyang Cho, Han-Wook Yoo, Jin-Ho Choi; Ann Pediatr Endocrinol Metab. 2014;19(1):32-35. Published online March 31, 2014; DOI: https://doi.org/10.6065/apem.2014.19.1.32
Crossref 6; 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


Insulin pump therapy in transient neonatal diabetes mellitus: Joong Heum Park, Jeong Hee Kang, Kyu-Hyung Lee, Nam-Hyo Kim, Han-Wook Yoo, Dae-Yeol Lee, Eun-Gyong Yoo; Ann Pediatr Endocrinol Metab. 2013;18(3):148-151. Published online September 30, 2013; DOI: https://doi.org/10.6065/apem.2013.18.3.148
Crossref 6; Full text PubReader ePub PDF


Turner syndrome with primary hyperparathyroidism: Jungmee Park, Yoo-Mi Kim, Jin-Ho Choi, Beom Hee Lee, Jong Ho Yoon, Woon-Young Jeong, Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 2013;18(2):85-89. Published online June 30, 2013; DOI: https://doi.org/10.6065/apem.2013.18.2.85
Crossref 4; 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 2; Full text PubReader ePub PDF


Steroidogenic Acute Regulatory Protein(StAR) Gene Mutation in two Korean Patients with Congenita1 Lipoid Adrenal Hyperplasia: Han-Wook Yoo, IlSoo Kim; Ann Pediatr Endocrinol Metab. 1996;1(1):69-77.; PDF


Molecular Genetic Screening for the SRY(Sex determining Region of the Y chromosome) Gene in Patients with Ambiguous Genitalia: Jun-Heui Seo, Han-Wook Yoo; Ann Pediatr Endocrinol Metab. 1996;1(1):105-112.; PDF

Journal Impact Factor 2.2

Editorial Office: 501-107, 30 Seocho-daero 74-gil, Seocho-gu, Seoul 06622, Republic of Korea
Tel: +82-2-3471-4268 Fax: +82-2-3471-4269 E-mail: editor@e-apem.org

Copyright © 2024 by Korean Society of Pediatric Endocrinology.

prev

next