- A case of Wolfram syndrome with chronic renal failure
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Korkmaz HA
- KMID: 2422483
- Ann Pediatr Endocrinol Metab.
- 2018 Sep;23(3):166-167.
- doi: 10.6065/apem.2018.23.3.166
No abstract available. -
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- Childhood diabetes in India
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Kalra S, Dhingra M
- KMID: 2422475
- Ann Pediatr Endocrinol Metab.
- 2018 Sep;23(3):126-130.
- doi: 10.6065/apem.2018.23.3.126
This review describes the epidemiology of childhood diabetes in India. It focuses on the incidence and prevalence of type 1 diabetes and its complications and comorbid conditions. The review also... -
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- Type 2 diabetes mellitus in children and adolescent: an Indonesian perspective
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Pulungan A, Afifa IT, Annisa D
- KMID: 2422474
- Ann Pediatr Endocrinol Metab.
- 2018 Sep;23(3):119-125.
- doi: 10.6065/apem.2018.23.3.119
The prevalence of type 2 diabetes mellitus (T2DM) in children and adolescents has increased globally over the past 2 decades. Metabolic syndrome, including obesity and overweight at a young age,... -
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- Testicular microlithiasis in a boy with X-linked adrenal hypoplasia congenita
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Serbis A, Tsinopoulou VR, Mouzaki K, Kotanidou , Giza S, Galli-Tsinopoulou A
- KMID: 2422482
- Ann Pediatr Endocrinol Metab.
- 2018 Sep;23(3):162-165.
- doi: 10.6065/apem.2018.23.3.162
X-linked adrenal hypoplasia congenita (AHC) is a rare disorder that usually presents clinically as adrenal insufficiency in early infancy. It is caused by mutations in the NR0B1 gene which is... -
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- Thyroid function in obese Korean children and adolescents: Korea National Health and Nutrition Examination Survey 2013–2015
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An YM, Moon SJ, Kim SK, Suh YJ, Lee JE
- KMID: 2422478
- Ann Pediatr Endocrinol Metab.
- 2018 Sep;23(3):141-147.
- doi: 10.6065/apem.2018.23.3.141
PURPOSE: In recent years, there has been an increasing focus on thyroid function in pediatric obese patients, but no nationwide study evaluating the relationship between thyroid function and obesity has... -
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- Clinical characteristics in Japanese children with nonobese type 2 diabetes
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Urakami T
- KMID: 2422473
- Ann Pediatr Endocrinol Metab.
- 2018 Sep;23(3):113-118.
- doi: 10.6065/apem.2018.23.3.113
It is well known that the incidence of youth-onset type 2 diabetes is increasing worldwide. On the other hand, most studies have shown that the majority of youth-onset type 2... -
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- Successful switching from insulin to sulfonylurea in a 3-month-old infant with diabetes due to p.G53D mutation in KCNJ11
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Yoon JS, Park KJ, Sohn YB, Lee HS, Hwang JS
- KMID: 2422480
- Ann Pediatr Endocrinol Metab.
- 2018 Sep;23(3):154-157.
- doi: 10.6065/apem.2018.23.3.154
Permanent neonatal diabetes mellitus is most commonly caused by mutations in the ATP-sensitive potassium channel (KATP) subunits. Prompt initiation of sulfonylurea treatment can improve glycemic control in children with KCNJ11... -
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- Therapeutic potential of alpha-1 antitrypsin in human disease
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Kim M, Cai Q, Oh Y
- KMID: 2422476
- Ann Pediatr Endocrinol Metab.
- 2018 Sep;23(3):131-135.
- doi: 10.6065/apem.2018.23.3.131
Alpha-1 antitrypsin (AAT), an alpha globulin glycoprotein, is a member of the serine protease inhibitor (serpin) superfamily. The clinical significance of AAT is highlighted by AAT deficiency. Genetic deficiency of... -
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- Evaluation of bone mineral status in prepuberal children with newly diagnosed type 1 diabetes
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Roh JG, Yoon JS, Park KJ, Lim JS, Lee HS, Hwang JS
- KMID: 2422477
- Ann Pediatr Endocrinol Metab.
- 2018 Sep;23(3):136-140.
- doi: 10.6065/apem.2018.23.3.136
PURPOSE: Many studies have reported that patients with type 1 diabetes have reduced bone mineral density (BMD). We assessed bone status in prepubertal children with type 1 diabetes mellitus (type... -
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- Factors affecting height velocity in normal prepubertal children
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Lee JH, Kim SK, Lee EK, Ahn MB, Kim SH, Cho WK, Cho KS, Jung MH, Suh BK
- KMID: 2422479
- Ann Pediatr Endocrinol Metab.
- 2018 Sep;23(3):148-153.
- doi: 10.6065/apem.2018.23.3.148
PURPOSE: To analyze the effects of clinical and laboratory factors, including insulin-like growth factor (IGF) levels, on the height velocity of normal prepubertal children. METHODS: Ninety-five healthy prepubertal children (33 boys,... -
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- Compound heterozygosity for a whole gene deletion and p.R124C mutation in CYP21A2 causing nonclassic congenital adrenal hyperplasia
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Nasir H, Ali SI, Haque N, Grebe SK, Kirmani S
- KMID: 2422481
- Ann Pediatr Endocrinol Metab.
- 2018 Sep;23(3):158-161.
- doi: 10.6065/apem.2018.23.3.158
We present a family with 2 members who received long-term steroid treatment for presumed classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, until molecular testing revealed nonclassic CAH, not... -
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