Annals of Pediatric Endocrinology & Metabolism

Search: Ann Pediatr Endocrinol Metab Search

CLOSE

Others

Page Path

HOME
ARTICLE CATEGORY
Others

Article Category


Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency: Jaebeen Kang, Min-Ji Kim, Sukdong Yoo, Chong Kun Cheon; Ann Pediatr Endocrinol Metab. 2024;29(3):201-203. Published online June 30, 2024; DOI: https://doi.org/10.6065/apem.2346236.118
Crossref 1; Full text PubReader ePub PDF


Commentary on "Long-read next-generation sequencing for molecular diagnosis of pediatric endocrine disorders": Won Kyoung Cho; Ann Pediatr Endocrinol Metab. 2024;29(3):141-141. Published online June 30, 2024; DOI: https://doi.org/10.6065/apem.24224014edi03; Full text PubReader ePub PDF


Orbital apex syndrome in pediatric thyroid eye disease: a case report and literature review: Hyun ji Jang, Ha young Jo; Ann Pediatr Endocrinol Metab. 2024;29(2):138-140. Published online January 29, 2024; DOI: https://doi.org/10.6065/apem.2346118.059; Full text PubReader ePub PDF


A novel compound heterozygous variant of the COL11A1 gene in a patient with fibrochondrogenesis type I: the first case in Korea: Jaesung Jeon, Minji Kim, Sukdong Yoo, Yoomi Kim, Chong Kun Cheon; Ann Pediatr Endocrinol Metab. 2024;29(2):135-137. Published online April 30, 2024; DOI: https://doi.org/10.6065/apem.2346150.075; Full text PubReader ePub PDF


Commentary on "Long-term endocrine sequelae after hematopoietic stem cell transplantation in children and adolescents": So Yoon Jung; Ann Pediatr Endocrinol Metab. 2024;29(2):73-74. Published online April 30, 2024; DOI: https://doi.org/10.6065/apem.2423023edi02; Full text PubReader ePub PDF


The first case of hyperosmolar diabetic ketoacidosis in a patient diagnosed with MODY 5 (maturity-onset diabetes of the young type 5) and 17q12 microdeletion syndrome: Jun Lee, Minji Kim, Sukdong Yoo, Ju Young Yoon, Chong Kun Cheon; Ann Pediatr Endocrinol Metab. 2024;29(1):70-72. Published online February 29, 2024; DOI: https://doi.org/10.6065/apem.2346006.003; Full text PubReader ePub PDF


Resistance to thyroid hormone and nonfunctioning pituitary microadenoma in a 13-year-old boy with THRB mutation: Jiyeon Kim, Eu Seon Noh, Min-Sun Kim, Jong-Moon Choi, Sae-Mi Lee, Sung Yoon Cho; Ann Pediatr Endocrinol Metab. 2024;29(1):67-69. Published online January 28, 2024; DOI: https://doi.org/10.6065/apem.2346056.028; Full text PubReader ePub PDF


Commentary on "Genetic evaluation using next-generation sequencing of children with short stature: a single tertiary-center experience": Hye Young Jin; Ann Pediatr Endocrinol Metab. 2024;29(1):1-2. Published online February 29, 2024; DOI: https://doi.org/10.6065/apem.2423018edi01; Full text PubReader ePub PDF


Commentary on "Effects of once-weekly dulaglutide on juvenile type 2 diabetes mellitus and obesity in Korea: a pilot study": Han Hyuk Lim; Ann Pediatr Endocrinol Metab. 2023;28(4):235-236. Published online December 31, 2023; DOI: https://doi.org/10.6065/apem.2322098edi010; Full text PubReader ePub PDF


Commentary on "Glycemic control and complications of type 2 diabetes mellitus in children and adolescents during the COVID-19 outbreak": Chong Kun Cheon; Ann Pediatr Endocrinol Metab. 2023;28(4):233-234. Published online December 31, 2023; DOI: https://doi.org/10.6065/apem.2322107edi009; Full text PubReader ePub PDF


Using low-dose octreotide with diazoxide-resistant congenital hyperinsulinism resulting from compound heterozygous mutations in the ABCC8 gene: Kyujung Park, Kyung In Lim, Young Bae Sohn, Hae Sang Lee, Jin Soon Hwang; Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S23-S24. Published online June 29, 2022; DOI: https://doi.org/10.6065/apem.2244068.034; Full text PubReader ePub PDF


Growth hormone deficiency in a boy with Wiedemann-Steiner syndrome: a case report and review: Mi Ra Kim, Eun-Gyong Yoo, Seonkyeong Rhie, Go Hun Seo, Mo Kyung Jung; Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S25-S28. Published online June 30, 2022; DOI: https://doi.org/10.6065/apem.2244052.026
Web of Science 2 Crossref 2; Full text PubReader ePub PDF


A novel compound variant in GNRHR causing congenital idiopathic hypogonadotropic hypogonadism in a young male Korean patient: Gimin Lee, Mi Seon Lee, Rosie Lee, Jung Eun Moon; Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S20-S22. Published online June 30, 2022; DOI: https://doi.org/10.6065/apem.2244070.035; Full text PubReader ePub PDF


A case of type A insulin resistance syndrome in a 14-year-old adolescent girl without common clinical features: Na won Lee, Ji Eun Jeong, Young Hwan Kim, Chang Seok Ki, Jin Kyung Kim; Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S17-S19. Published online February 1, 2023; DOI: https://doi.org/10.6065/apem.2244106.053
Web of Science 1; Full text PubReader ePub PDF


Turner syndrome due to Xp22.33 deletion combined with 7p22.3 duplication: Ha young Jo, Hyun Ji Jang, Young Mi Kim, Soo-Han Choi, Kyung Hee Park, Hye Won Yoo, Su Jeong Park, Yoon Hee Jo, Min Jung Kwak; Ann Pediatr Endocrinol Metab. 2023;28(Suppl 1):S14-S16. Published online February 1, 2023; DOI: https://doi.org/10.6065/apem.2244122.061; Full text PubReader ePub PDF

Journal Impact Factor 2.8

Pediatrics Q1

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 © 2025 by Korean Society of Pediatric Endocrinology.

prev

next