Article List

WPRIM Management System> DCMS> Chinese Journal of Applied Clinical Pediatrics> 2016> 31> 8

Volume: 31 Issue: 8

1. Small supernumerary marker chromosome and chromosome 18p abnormalities	Page:561—564
2. Application of recombinant human growth hormone in treatment of Prader-Willi syndrome	Page:564—568
3. Clinical and molecular characteristics of 27 children with Prader-Willi syndrome in South China	Page:573—578
4. Scanning and analysis of the KATP channel mutations in 12 cases of infancy onset type 1 diabetes mellitus	Page:579—583
5. Significance of thyroid stimulating antibody and thyroid stimulating-blocking antibody in children with autoimmune thyroid disease	Page:600—603
6. Clinical and genetic study on a family with metatropic dysplasia due to transient receptor potential vanilloid 4 gene mutation	Page:609—612
7. Mitochondrial diseases with the main manifestations of cardiomyopathy and respiratory muscle damage	Page:613—615
8. Effects of dead box 1 gene on invasion, migration and drug resistance capability of neuroblastoma cells	Page:616—619
9. Analysis of clinical outcome and treatment of viral encephalitis with bilateral thalamic damage	Page:620—623
10. Research progress of metabolic syndrome in children with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency	Page:631—634
11. The impact of management program for children with diabetes in China on the glycemic control of type 1 diabetic mellitus children and factors associated with glycemic control	Page:584—587
12. The therapeutic effect and safety of recombinant human growth hormone in short children born small for gestational age	Page:588—591
13. Genetic pathogenesis and current trends in diagnosis and therapy of ATP-sensitive potassium channel congenital hyperinsulinism	Page:628—630
14. Advances in studies on biotinidase deficiency	Page:637—640
15. Progress in the correlation between thyroid stimulating hormone receptor gene and hyperthyroidism	Page:634—637