Mitochondrial uncoupling protein 2 (UCP2) gene polymorphisms are associated with childhood obesity and related metabolic disorders

Articles in the same Issue

1. Masthead
2. Masthead
3. Editorial
4. Premature adrenarche: not always benign?
5. Review Article
6. From fat cell biology to public health preventive strategies – pinpointing the critical period for obesity prevention
7. Images in Pediatric Endocrinology
8. Pituitary macroadenoma due to hypothyroidism
9. Parathyroid adenoma presented with multiple brown tumors and nephrocalcinosis
10. Original Articles
11. In children with premature adrenarche, bone age advancement by 2 or more years is common and generally benign
12. Accelerated early pubertal progression, ovarian morphology, and ovarian function in prospectively followed low birth weight (LBW) girls
13. Long-term secular trend of skeletal maturation of Taiwanese children between agricultural (1960s) and contemporary (after 2000s) generations using the Tanner-Whitehouse 3 (TW3) method
14. Influence of developmental and hormonal factors on bone health in adolescent females: a cross-sectional study and review of the literature
15. Predicting growth response among Egyptian prepubertal idiopathic isolated growth hormone deficient children
16. Egyptian growth hormone deficient patients: demographic, auxological characterization and response to growth hormone therapy
17. Improved metabolic and cardiorespiratory fitness during a recreational training program in obese children
18. Mitochondrial uncoupling protein 2 (UCP2) gene polymorphisms are associated with childhood obesity and related metabolic disorders
19. OGTT results in obese adolescents with normal HOMA-IR values
20. Type of infectious disease affects glucose metabolism and liver glycogen content in Surinamese children: malaria vs. pneumonia
21. Cognitive and developmental outcome of conservatively treated children with congenital hyperinsulinism
22. Protective mechanisms against oxidative stress and angiopathy in young patients with diabetes type 1 (DM1)
23. Glucose metabolism in obese and lean adolescents with polycystic ovary syndrome
24. Morbidity characteristics of patients with congenital insensitivity to pain with anhidrosis (CIPA)
25. Age-related reference values for plasma amino acids in a Spanish population measured by gas chromatography-mass spectrometry
26. Bupropion can close K_ATP channel and induce insulin secretion
27. Children at risk of diabetes type 1. Treatment with acetyl-L-carnitine plus nicotinamide – Case reports
28. Patient Reports
29. A boy with prepubertal gynecomastia, hyperprolactinemia, and hypothyroidism
30. Growth hormone deficiency and central precocious puberty in Klinefelter syndrome: report of a case and review of KIGS database
31. Parathyroid hormone-independent hypercalcemia in an infant with renal dysplasia: possible role of PTHrP
32. Bilateral pheochromocytomas in a child who had hemihypertrophy and alteration in the VHL gene
33. Autoimmune polyglandular syndrome type 1 with reversible dilated cardiomyopathy: complete recovery after correction of hypocalcemia and hypocortisolemia
34. Zellweger syndrome — a lethal peroxisome biogenesis disorder
35. First seizure as late presentation of velo-cardio-facial syndrome
36. A novel mutation in a mother and a son with Aarskog-Scott syndrome
37. Clinical and genetic characterization of a Chinese patient with triple A syndrome and novel compound heterozygous mutations in the AAAS gene
38. Pseudohypoaldosteronism presenting with thrombocytosis and bilateral pneumothoraces in an infant
39. Letter to the Editors
40. Interferon-γ (IFN-γ) in endometriosis: the conjunction point between the retrograde menstruation theory and the inflammatory hypothesis
41. Methylmalonic aciduria: newborn screening in mainland China?
42. Hypophosphatemia in small gestational age extremely low birth weight infants and bone metabolic status parameters