- Giant juvenile fibroadenoma of the breast: a case report and brief literature review
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Song BS, Kim EK, Seol H, Seo JH, Lee JA, Kim DH, Lim JS
- KMID: 1702664
- Ann Pediatr Endocrinol Metab.
- 2014 Mar;19(1):45-48.
- doi: 10.6065/apem.2014.19.1.45
A girl (age, 12 years 11 months) consulted the pediatric endocrinology clinic because of a rapidly growing right breast mass over 13 cm observed during the preceding 3 months. A... -
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- Iodine and thyroid function
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Chung HR
- KMID: 1702657
- Ann Pediatr Endocrinol Metab.
- 2014 Mar;19(1):8-12.
- doi: 10.6065/apem.2014.19.1.8
Severe iodine deficiency causes hypothyroidism that results in impaired somatic growth and motor development in children. Mild and moderate iodine deficiencies cause multifocal autonomous growth of thyroid, which results in... -
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- Glycogenic hepatopathy in a Korean girl with poorly controlled type 1 diabetes mellitus
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Jeong HR, Shim YS, Kim YB, Lee HS, Hwang JS
- KMID: 1702665
- Ann Pediatr Endocrinol Metab.
- 2014 Mar;19(1):49-52.
- doi: 10.6065/apem.2014.19.1.49
Glycogenic hepatopathy (GH) is a rare complication of type 1 diabetes mellitus. We report the case of a 13-year-old diabetic female with poorly controlled blood sugar levels who presented with... -
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- Mosaic Turner syndrome associated with schizophrenia
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Jung SY, Park JW, Kim DH, Jun YH, Lee JS, Lee JE
- KMID: 1702663
- Ann Pediatr Endocrinol Metab.
- 2014 Mar;19(1):42-44.
- doi: 10.6065/apem.2014.19.1.42
Turner syndrome is a sex-chromosome disorder; occurring in 1 in 2,500 female births. There are sporadic few case reports of concomitant Turner syndrome with schizophrenia worldwide. Most Turner females had... -
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- Serum vitamin D status in children and adolescence with diabetes according to season and age
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Jung SS, Kim MS, Lee DY
- KMID: 1702658
- Ann Pediatr Endocrinol Metab.
- 2014 Mar;19(1):13-19.
- doi: 10.6065/apem.2014.19.1.13
PURPOSE: It is known that children with diabetes have more severe vitamin D deficiency than healthy children. This study aimed to investigate serum vitamin D status and analyze the relationships... -
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- Age of menarche and near adult height after long-term gonadotropin-releasing hormone agonist treatment in girls with central precocious puberty
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Baek JW, Nam HK, Jin D, Oh YJ, Rhie YJ, Lee KH
- KMID: 1702660
- Ann Pediatr Endocrinol Metab.
- 2014 Mar;19(1):27-31.
- doi: 10.6065/apem.2014.19.1.27
PURPOSE: Gonadotropin-releasing hormone agonist (GnRHa) is known for improving final adult height in patients with central precocious puberty (CPP). This study aimed to investigate the age of menarche and near... -
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- Efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency
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Kim JH, Cho JH, Yoo HW, Choi JH
- KMID: 1702661
- Ann Pediatr Endocrinol Metab.
- 2014 Mar;19(1):32-35.
- doi: 10.6065/apem.2014.19.1.32
PURPOSE: Growth hormone (GH) plays a key role in the regulation of body composition, lipid metabolism, and quality of life in adults with GH deficiency (GHD). This study investigated changes... -
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- Clinical and radiological findings of incidental Rathke's cleft cysts in children and adolescents
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Oh YJ, Park HK, Yang S, Song JH, Hwang IT
- KMID: 1702659
- Ann Pediatr Endocrinol Metab.
- 2014 Mar;19(1):20-26.
- doi: 10.6065/apem.2014.19.1.20
PURPOSE: In the pediatric population, Rathke's cleft cysts (RCCs) are known to be an infrequent cause of headaches, visual disturbances, and pituitary dysfunction. We investigated the clinical characteristics of children... -
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- Growth hormone treatment in non-growth hormone-deficient children
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Loche S, Carta L, Ibba A, Guzzetti C
- KMID: 1702656
- Ann Pediatr Endocrinol Metab.
- 2014 Mar;19(1):1-7.
- doi: 10.6065/apem.2014.19.1.1
Until 1985 growth hormone (GH) was obtained from pituitary extracts, and was available in limited amounts only to treat severe growth hormone deficiency (GHD). With the availability of unlimited quantities... -
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- A novel de novo mutation within PHEX gene in a young girl with hypophosphatemic rickets and review of literature
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Cheon CK, Lee HS, Kim SY, Kwak MJ, Kim GH, Yoo HW
- KMID: 1702662
- Ann Pediatr Endocrinol Metab.
- 2014 Mar;19(1):36-41.
- doi: 10.6065/apem.2014.19.1.36
X-linked hypophosphatemia (XLH) is the most common form of familial hypophosphatemic rickets and it is caused by loss-of-function mutations in the PHEX gene. Recently, a wide variety of PHEX gene... -
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