- Updates on bone health in children with gastrointestinal diseases
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Yang HR
- KMID: 2501031
- Ann Pediatr Endocrinol Metab.
- 2020 Mar;25(1):10-14.
- doi: 10.6065/apem.2020.25.1.10
Chronic gastrointestinal diseases such as inflammatory bowel disease, malabsorption syndromes (e.g., intestinal lymphangiectasia, celiac disease, congenital chloride diarrhea, cystic fibrosis), and postsubtotal gastrectomy state or short-bowel syndrome after extensive bowel... -
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- Bone morbidity in pediatric acute lymphoblastic leukemia
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Ahn MB, Suh BK
- KMID: 2501030
- Ann Pediatr Endocrinol Metab.
- 2020 Mar;25(1):1-9.
- doi: 10.6065/apem.2020.25.1.1
Acute lymphoblastic leukemia (ALL), currently the most common pediatric leukemia, has a high curability rate of up to 90%. Endocrine disorders are highly prevalent in children with ALL, and skeletal... -
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- Bone health in pediatric patients with neurological disorders
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Ko A, Kong J, Samadov F, Mukhamedov A, Kim YM, Lee YJ, Nam SO
- KMID: 2501032
- Ann Pediatr Endocrinol Metab.
- 2020 Mar;25(1):15-23.
- doi: 10.6065/apem.2020.25.1.15
Patients with neurological disorders are at high risk of developing osteoporosis, as they possess multiple risk factors leading to low bone mineral density. Such factors include inactivity, decreased exposure to... -
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- Comparison of proinsulin to C-peptide ratio in children with and without type 1 diabetes and its relation to age
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Ellison BR, Burton JH, Hsia DS
- KMID: 2501035
- Ann Pediatr Endocrinol Metab.
- 2020 Mar;25(1):38-41.
- doi: 10.6065/apem.2020.25.1.38
Purpose: This study aimed to compare the proinsulin to C-peptide (PI:C) ratio in those with recent-onset type 1 diabetes versus those with no diabetes and to explore the effect of... -
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- A homozygous mutation in the insulin gene (INS) causing autosomal recessive neonatal diabetes in Saudi families
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Shaikh AA, Shirah B, Alzelaye S
- KMID: 2501036
- Ann Pediatr Endocrinol Metab.
- 2020 Mar;25(1):42-45.
- doi: 10.6065/apem.2020.25.1.42
Purpose: Insulin gene (INS) mutations are a rare cause of permanent neonatal diabetes and mature-onset diabetes of the young (MODY10). Homozygous mutations have been reported to cause diabetes by decreasing... -
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- Identification of a novel variant in the PHEX gene using targeted gene panel sequencing in a 24-month-old boy with hypophosphatemic rickets
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Jo HY, Shin JH, Kim HY, Kim YM, Lee H, Bae MH, Park KH, Jang JH, Kwak MJ
- KMID: 2501040
- Ann Pediatr Endocrinol Metab.
- 2020 Mar;25(1):63-67.
- doi: 10.6065/apem.2020.25.1.63
Familial hypophosphatemic rickets (FHR) is a disorder characterized by phosphate wasting and hypophosphatemia due to defects in renal phosphate transport regulation. There are 4 known inherited forms of FHR that... -
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- Effect of -202 A/C IGFBP-3 polymorphisms on growth responses in children with idiopathic short stature
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Kang HR, Hwang IT, Yang S
- KMID: 2501034
- Ann Pediatr Endocrinol Metab.
- 2020 Mar;25(1):31-37.
- doi: 10.6065/apem.2020.25.1.31
Purpose: This study evaluated the -202 A/C insulin-like growth factor binding protein 3 (IGFBP-3) promoter polymorphism as a predictor of serum IGFBP-3 concentration and growth velocity after recombinant growth hormone... -
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- Persistent goiter with congenital hypothyroidism due to mutation in DUOXA2 gene
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Jung SY, Lee J, Lee DH
- KMID: 2501039
- Ann Pediatr Endocrinol Metab.
- 2020 Mar;25(1):57-62.
- doi: 10.6065/apem.2020.25.1.57
Thyroid hormones are crucial for development of the central nervous system. Congenital hypothyroidism (CH) is the most common preventable disease resulting in mental retardation. A neonatal screening test (NST) can... -
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- Nonclassic congenital lipoid adrenal hyperplasia diagnosed at 17 months in a Korean boy with normal male genitalia: emphasis on pigmentation as a diagnostic clue
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Bae H, Kim MS, Park H, Jang JH, Choi JM, Lee SM, Cho SY, Jin DK
- KMID: 2501037
- Ann Pediatr Endocrinol Metab.
- 2020 Mar;25(1):46-51.
- doi: 10.6065/apem.2020.25.1.46
Congenital lipoid adrenal hyperplasia (CLAH) is one of the most fatal conditions caused by an abnormality of adrenal and gonadal steroidogenesis. CLAH results from loss-of-function mutations of the steroidogenic acute... -
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- Relationship between final adult height and birth weight after gonadotropin-releasing hormone agonist treatment in girls with central precocious puberty
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Cho AY, Ko SY, Lee JH, Kim EY
- KMID: 2501033
- Ann Pediatr Endocrinol Metab.
- 2020 Mar;25(1):24-30.
- doi: 10.6065/apem.2020.25.1.24
Purpose: The clinical significance of birth weight relative to gestational age in girls with central precocious puberty is unclear. This study sought to compare clinical parameters such as final adult... -
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- Successful rapid weight reduction and the use of liraglutide for morbid obesity in adolescent Prader-Willi syndrome
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Kim YM, Lee YJ, Kim SY, Cheon CK, Lim HH
- KMID: 2501038
- Ann Pediatr Endocrinol Metab.
- 2020 Mar;25(1):52-56.
- doi: 10.6065/apem.2020.25.1.52
Prader-Willi syndrome (PWS), an imprinting disorder, results from the loss of expression of a paternal gene on chromosome 15q11-q13. Progressive obesity and its associated complications lead to increased morbidity and... -
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