Previous Issue   Volume 26(1); Mar 2021
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Issues
Role of obesity-induced inflammation in the development of insulin resistance and type 2 diabetes: history of the research and remaining questions
Jieun Kim, Jongsoon Lee
Ann Pediatr Endocrinol Metab. 2021;26(1):1-13.
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Dairy consumption and risk of type-2 diabetes: the untold story
Sai Krishna Gudi
Ann Pediatr Endocrinol Metab. 2021;26(1):14-18.
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Complete androgen insensitivity syndrome and risk of gonadal malignancy: systematic review
Beatriz Amstalden Barros, Letícia Ribeiro de Oliveira, Cíntia Regina Crocetti Surur, Antonio de Azevedo Barros-Filho, Andrea Trevas Maciel-Guerra, Gil Guerra-Junior
Ann Pediatr Endocrinol Metab. 2021;26(1):19-23.
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A cell function study on calcium regulation of a novel calcium-sensing receptor mutation (p.Tyr825Phe)
Jung Eun Moon, Hee-Young Yang, Gabbine Wee, Suk-Hyun ParK, Cheol Woo Ko
Ann Pediatr Endocrinol Metab. 2021;26(1):24-30.
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Factors influencing growth hormone therapy effect during the prepubertal period in small for gestational age children without catch-up growth
Chang Dae Kum, Jung Gi Rho, Hong Kyu Park, Hae Sang Lee, Jin Soon Hwang
Ann Pediatr Endocrinol Metab. 2021;26(1):31-37.
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Changes in anthropometric indices among Korean school students based on the 2010 and 2018 Korea School Health Examination Surveys
Moon Young Seo, Shin-Hye Kim, Mi Jung Park
Ann Pediatr Endocrinol Metab. 2021;26(1):38-45.
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Novel function of adrenocorticotropic hormone in the stimulation of vascular endothelial growth factor release in healthy children and adolescents: a proof-of-concept study
Ryan Heksch, Sasigarn Bowden, Robert Hoffman
Ann Pediatr Endocrinol Metab. 2021;26(1):46-52.
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Thyroid imaging study in children with suspected thyroid dysgenesis
Sangwoo Chun, Young Seok Lee, Jeesuk Yu
Ann Pediatr Endocrinol Metab. 2021;26(1):53-59.
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Congenital hyperinsulinism: 2 case reports with different rare variants in ABCC8
Julie Mouron-Hryciuk, Sophie Stoppa-Vaucher, Kanetee Busiah, Thérèse Bouthors, Maria Christina Antoniou, Eric Jacot, Klaus Brusgaard, Henrik Thybo Christesen, Khalid Hussain, Andrew Dwyer, Matthias Roth-Kleiner, Michael Hauschild
Ann Pediatr Endocrinol Metab. 2021;26(1):60-65.
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Two cases of 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 mutation
Hae In Lee, Ahreum Kwon, Jung Hwan Suh, Han Saem Choi, Kyung Chul Song, Hyun Wook Chae, Ho-Seong Kim
Ann Pediatr Endocrinol Metab. 2021;26(1):66-70.
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