- The current state of dyslipidemia in Korean children and adolescents and its management in clinical practice
-
Lim JS
- KMID: 1429671
- Ann Pediatr Endocrinol Metab.
- 2013 Mar;18(1):1-8.
- doi: 10.6065/apem.2013.18.1.1
Cardiovascular disease (CVD) is a leading cause of death worldwide including Korea. The risk factors of CVD are known as positive family history of early CVD, obesity, hypertension, diabetes, and... -
- CITED
-
- Close
- SHARE
-
- Close
- Role of insulin-like growth factor binding protein-3 in glucose and lipid metabolism
-
Kim HS
- KMID: 1429672
- Ann Pediatr Endocrinol Metab.
- 2013 Mar;18(1):9-12.
- doi: 10.6065/apem.2013.18.1.9
Insulin-like growth factor binding protein (IGFBP)-3 has roles in modulating the effect of IGFs by binding to IGFs and inhibiting cell proliferation in an IGF-independent manner. Although recent studies have... -
- CITED
-
- Close
- SHARE
-
- Close
- Insulin autoimmune syndrome induced by methimazole in a Korean girl with Graves' disease
-
Lee SH, Oh SH, Chung WY
- KMID: 1429679
- Ann Pediatr Endocrinol Metab.
- 2013 Mar;18(1):32-35.
- doi: 10.6065/apem.2013.18.1.32
Hypoglycemia was detected in a 15-year-old girl due to loss of consciousness. She was diagnosed with Graves' disease and was being treated with methimazole for the past 4 months. A... -
- CITED
-
- Close
- SHARE
-
- Close
- Response to three years of growth hormone therapy in girls with Turner syndrome
-
Park HK, Lee HS, Ko JH, Hwang IT, Hwang JS
- KMID: 1429673
- Ann Pediatr Endocrinol Metab.
- 2013 Mar;18(1):13-18.
- doi: 10.6065/apem.2013.18.1.13
PURPOSE: Short stature is the most common finding in patients with Turner syndrome. Improving the final adult height in these patients is a challenge both for the patients and physicians.... -
- CITED
-
- Close
- SHARE
-
- Close
- Gitelman syndrome combined with complete growth hormone deficiency
-
Min SR, Cho HS, Hong J, Cheong HI, Ahn SY
- KMID: 1429681
- Ann Pediatr Endocrinol Metab.
- 2013 Mar;18(1):36-39.
- doi: 10.6065/apem.2013.18.1.36
Gitelman syndrome is a rare autosomal recessive hereditary salt-losing tubulopathy, that manifests as hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria. It is caused by mutations in the solute carrier family 12(sodium/chloride... -
- CITED
-
- Close
- SHARE
-
- Close
- Different clinical courses of central precocious girls according to their age at presentation and treatment
-
Yoon SA, Han HS, Kim H, Yun SC
- KMID: 1429675
- Ann Pediatr Endocrinol Metab.
- 2013 Mar;18(1):19-25.
- doi: 10.6065/apem.2013.18.1.19
PURPOSE: The progressivity of central precocious puberty (CPP) seems to depend on the age at presentation. We evaluated the clinical courses of CPP girls according to their age at initiation... -
- CITED
-
- Close
- SHARE
-
- Close
- p.R182C mutation in Korean twin with congenital lipoid adrenal hyperplasia
-
Park HW, Kwak BO, Kim GH, Yoo HW, Chung S
- KMID: 1429683
- Ann Pediatr Endocrinol Metab.
- 2013 Mar;18(1):40-43.
- doi: 10.6065/apem.2013.18.1.40
Congenital lipoid adrenal hyperplasia (CLAH) is the most severe form of congenital adrenal hyperplasia which is caused by mutations in the steroidogenic acute regulatory protein (StAR). The mutations in StAR... -
- CITED
-
- Close
- SHARE
-
- Close
- Combined aerobic and resistance exercise is effective for achieving weight loss and reducing cardiovascular risk factors without deteriorating bone health in obese young adults
-
Lim JS, Jang GC, Moon KR, Kim EY
- KMID: 1429676
- Ann Pediatr Endocrinol Metab.
- 2013 Mar;18(1):26-31.
- doi: 10.6065/apem.2013.18.1.26
PURPOSE: Weight loss reduces cardiovascular risk factors in the obese. However, weight reduction through diet negatively affects long-term bone health. The aim of study was to determine the ability of... -
- CITED
-
- Close
- SHARE
-
- Close
