Annals of Pediatric Endocrinology & Metabolism

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27 Articles


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 Crossref - TDM 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; Full text PubReader ePub Crossref - TDM 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; Full text PubReader ePub Crossref - TDM 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; Full text PubReader ePub Crossref - TDM 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
Cited By 5; Full text PubReader ePub Crossref - TDM 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
Cited By 1; Full text PubReader ePub Crossref - TDM 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
Cited By 6; Full text PubReader ePub Crossref - TDM 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
Cited By 3; Full text PubReader ePub Crossref - TDM 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
Cited By 6; Full text PubReader ePub Crossref - TDM 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
Cited By 16; Full text PubReader ePub Crossref - TDM 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
Cited By 5; Full text PubReader ePub Crossref - TDM 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; Full text PubReader ePub Crossref - TDM 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
Cited By 3; Full text PubReader ePub Crossref - TDM 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
Cited By 4; Full text PubReader ePub Crossref - TDM 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
Cited By 17; Full text PubReader ePub Crossref - TDM 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
Cited By 21; Full text PubReader ePub Crossref - TDM 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
Cited By 14; Full text PubReader ePub Crossref - TDM 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
Cited By 5; Full text PubReader ePub Crossref - TDM 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
Cited By 24; Full text PubReader ePub Crossref - TDM 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
Cited By 2; Full text PubReader ePub Crossref - TDM 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
Cited By 5; Full text PubReader ePub Crossref - TDM 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
Cited By 8; Full text PubReader ePub Crossref - TDM 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
Cited By 5; Full text PubReader ePub Crossref - TDM 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
Cited By 2; Full text PubReader ePub Crossref - TDM 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
Cited By 2; Full text PubReader ePub Crossref - TDM 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

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