- Dairy consumption and risk of type-2 diabetes: the untold story
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Gudi SK
- KMID: 2514147
- Ann Pediatr Endocrinol Metab.
- 2021 Mar;26(1):14-18.
- doi: 10.6065/apem.2040074.037
The role of dairy products in human health has been extensively studied for decades; however, evidence regarding dairy consumption and risk of type 2 diabetes (T2D) remains controversial and uncertain.... -
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- Two cases of 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 mutation
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Lee HI, Kwon A, Suh JH, Choi HS, Song KC, Chae HW, Kim HS
- KMID: 2514155
- Ann Pediatr Endocrinol Metab.
- 2021 Mar;26(1):66-70.
- doi: 10.6065/apem.2040184.092
17α-hydroxylase/17,20-lyase deficiency, caused by mutations in the cytochrome P450 family 17 subfamily A member 1 gene (CYP17A1), is an extremely rare form of congenital adrenal hyperplasia that is characterized by... -
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- Thyroid imaging study in children with suspected thyroid dysgenesis
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Chun S, Lee YS, Yu J
- KMID: 2514153
- Ann Pediatr Endocrinol Metab.
- 2021 Mar;26(1):53-59.
- doi: 10.6065/apem.2040120.060
Purpose: Thyroid dysgenesis is one of the most common causes of permanent congenital hypothyroidism. Thyroid ultrasonography or scan is used to detect thyroid dysgenesis. We analyzed the sensitivity and specificity... -
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- Congenital hyperinsulinism: 2 case reports with different rare variants in ABCC8
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Mouron-Hryciuk J, Stoppa-Vaucher S, Busiah K, Bouthors T, Antoniou MC, Jacot E, Brusgaard K, Christesen HT, Hussain K, Dwyer A, Roth-Kleiner M, Hauschild M
- KMID: 2514154
- Ann Pediatr Endocrinol Metab.
- 2021 Mar;26(1):60-65.
- doi: 10.6065/apem.2040042.021
Congenital hyperinsulinism (CHI) is a rare glucose metabolism disorder characterized by unregulated secretion of insulin that leads to hyperinsulinemic hypoglycemia (HH). Most cases are caused by mutations in the KATP-channel... -
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- Changes in anthropometric indices among Korean school students based on the 2010 and 2018 Korea School Health Examination Surveys
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Seo MY, Kim SH, Park MJ
- KMID: 2514151
- Ann Pediatr Endocrinol Metab.
- 2021 Mar;26(1):38-45.
- doi: 10.6065/apem.2040100.050
Purpose: This study sought to identify changes in anthropometric values among Korean school students by comparing the most recent nationwide data with previous data. Methods: Data from the Korea School Health... -
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- Role of obesity-induced inflammation in the development of insulin resistance and type 2 diabetes: history of the research and remaining questions
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Kim J, Lee J
- KMID: 2514146
- Ann Pediatr Endocrinol Metab.
- 2021 Mar;26(1):1-13.
- doi: 10.6065/apem.2040188.094
The prevalence of obesity has increased alarmingly both worldwide and in Korea. This has also dramatically increased the prevalence of chronic obesity-associated diseases, including type 2 diabetes (T2D). Extensive studies... -
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- Complete androgen insensitivity syndrome and risk of gonadal malignancy: systematic review
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Barros BA, Oliveira LRd, Surur CRC, Barros-Filho AdA, Maciel-Guerra AT, Guerra-Junior G
- KMID: 2514148
- Ann Pediatr Endocrinol Metab.
- 2021 Mar;26(1):19-23.
- doi: 10.6065/apem.2040170.085
Complete androgen insensitivity syndrome (CAIS) is a rare condition characterized by 46,XY karyotype, female external genitalia, absence of uterus, and testes located intra-abdominally, in the inguinal ring or in the... -
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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
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Heksch R, Bowden S, Hoffman R
- KMID: 2514152
- Ann Pediatr Endocrinol Metab.
- 2021 Mar;26(1):46-52.
- doi: 10.6065/apem.2040110.055
Purpose: To assess the effect of adrenocorticotropic hormone (ACTH) on plasma vascular endothelial growth factor (VEGF) levels in healthy children and adolescents and to inform future work on the effects... -
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- A cell function study on calcium regulation of a novel calcium-sensing receptor mutation (p.Tyr825Phe)
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Moon JE, Yang HY, Wee G, ParK SH, Ko CW
- KMID: 2514149
- Ann Pediatr Endocrinol Metab.
- 2021 Mar;26(1):24-30.
- doi: 10.6065/apem.2040022.011
Purpose: Autosomal dominant hypocalcemia with hypercalciuria is a genetic disease characterized by hypoparathyroidism with hypercalciuria. We discovered a novel variant (p.Tyr825Phe[Y825F]) of the CASR gene in a neonate with congenital... -
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- Factors influencing growth hormone therapy effect during the prepubertal period in small for gestational age children without catch-up growth
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Kum CD, Rho JG, Park HK, Lee HS, Hwang JS
- KMID: 2514150
- Ann Pediatr Endocrinol Metab.
- 2021 Mar;26(1):31-37.
- doi: 10.6065/apem.2040096.048
Purpose: Because small for gestational age (SGA) children who fail to experience catch-up growth have an increased risk of short stature in adulthood, growth hormone (GH) treatment is recommended for... -
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