Delayed cord clamping in full-term neonates: is it time for outlining exclusion criteria?

Articles in the same Issue

1. Masthead
2. Masthead
3. Review Article
4. Clinical and diagnostic characteristics of hyperprolactinemia in childhood and adolescence
5. Images in Pediatric Endocrinology
6. Early occurrence of cerebral white matter abnormality detected in a neonate with salt-wasting congenital adrenal hyperplasia
7. Original Articles
8. Pentoxifylline treatment for protecting diabetic retinopaty in children with type 1 diabetes
9. Absence of diabetes mellitus type 2 in obese children and adolescents in the north of Spain
10. Ceramide mediates inhibition of the Akt/eNOS pathway by high levels of glucose in human vascular endothelial cells
11. Short- and middle-term continuous use of cinacalcet in children on peritoneal dialysis
12. Congenital hypothyroidism caused by a novel mutation of the dual oxidase 2 (DUOX2) gene
13. Arginine-guanidinoacetate-creatine pathway in preterm newborns: creatine biosynthesis in newborns
14. The effect of different nutritional states on puberty onset and the expression of hypothalamic Kiss1/kisspepetin
15. Celiac disease and dermatitis herpetiformis in Brazilian twins: a long-term follow-up and screening of their relatives
16. Glucocorticoid receptor expression in whole blood with preterm infants
17. Trends in hospitalizations among children with type 1 diabetes in Spain, 2001–2009
18. Effects of a combined intervention for treating severely obese prepubertal children
19. Vitamin D levels, insulin resistance, and cardiovascular risks in very young obese children
20. Prevalence of metabolic syndrome in children and adolescents — the recent trends in South Korea
21. Elevated visfatin levels in obese children are related to proinflammatory factors
22. Patient reports
23. A clinically euthyroid child with a large goiter due to a thyroglobulin gene defect: clinical features and genetic studies
24. Immune thrombocytopenic purpura in a child with thyroid hormone resistance – a rare presentation
25. Attempted suicide with levothyroxine in an adolescent girl
26. Differentiated thyroid carcinoma in a girl with resistance to thyroid hormone management with triiodothyroacetic acid
27. Brothers with germline PTEN mutations and persistent hypoglycemia, macrocephaly, developmental delay, short stature, and coagulopathy
28. DEND syndrome due to V59A mutation in KCNJ11 gene: unresponsive to sulfonylureas
29. Severe short stature due to 3-M syndrome with a novel OBSL1 gene mutation
30. Mild form of 3-methylglutaconic aciduria type IV and mutation in the TMEM70 genes
31. Conn syndrome and Crohn disease in a pediatric case: an interesting parallel
32. Adolescent ischemic stroke associated with anabolic steroid and cannabis abuse
33. Anorexia nervosa in a patient with congenital adrenal hyperplasia
34. Severe hypothalamopituitary dysfunction accompanied by influenza-associated encephalopathy: report of two pediatric cases
35. Octreotide-induced hepatitis in a child with persistent hyperinsulinemia hypoglycemia of infancy
36. Hepatitis in an infant treated with octreotide for congenital hyperinsulinism
37. Letters to the Editor
38. Delayed cord clamping in full-term neonates: is it time for outlining exclusion criteria?
39. And what about cord blood cardiac troponin I (cTnI) levels as an inclusion criterion for therapeutic hypothermia after perinatal asphyxia?
40. Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD
41. Association of the interferon-γ (IFN-γ) gene polymorphism with endometriosis: is epidermal growth factor (EGF) the key-mediator?