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

Volume: 31 Issue: 8

1. Progress in the correlation between thyroid stimulating hormone receptor gene and hyperthyroidism Page:634—637
2. Small supernumerary marker chromosome and chromosome 18p abnormalities Page:561—564
3. Application of recombinant human growth hormone in treatment of Prader-Willi syndrome Page:564—568
4. Clinical and molecular characteristics of 27 children with Prader-Willi syndrome in South China Page:573—578
5. Scanning and analysis of the KATP channel mutations in 12 cases of infancy onset type 1 diabetes mellitus Page:579—583
6. Significance of thyroid stimulating antibody and thyroid stimulating-blocking antibody in children with autoimmune thyroid disease Page:600—603
7. Clinical and genetic study on a family with metatropic dysplasia due to transient receptor potential vanilloid 4 gene mutation Page:609—612
8. Mitochondrial diseases with the main manifestations of cardiomyopathy and respiratory muscle damage Page:613—615
9. Effects of dead box 1 gene on invasion, migration and drug resistance capability of neuroblastoma cells Page:616—619
10. Analysis of clinical outcome and treatment of viral encephalitis with bilateral thalamic damage Page:620—623
11. Research progress of metabolic syndrome in children with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Page:631—634
12. 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
13. The therapeutic effect and safety of recombinant human growth hormone in short children born small for gestational age Page:588—591
14. Genetic pathogenesis and current trends in diagnosis and therapy of ATP-sensitive potassium channel congenital hyperinsulinism Page:628—630
15. Advances in studies on biotinidase deficiency Page:637—640
16. Case report of Gentamicin-induced Bartter-like syndrome Page:626—627

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