Volume: 35 Issue: 9

1. Clinical characteristics, plasma levels of hydrogen sulfide and gene analysis of cardiovascular involvement in children with methylmalonic acidemia and homocystinemia Page:681—685
2. Surgical treatment of deep brain stimulation for pediatric hereditary dystonia Page:662—666
3. Dietary and nutritional intervention of Prader-Willi syndrome Page:677—680
4. Pedigree analysis of Xp21 contiguous gene deletion syndrome and literature review Page:695—699
5. Inherited metabolic diseases that are prone to cause the impairment of lung function Page:671—676
6. Monogenic nephrolithiasis Page:667—670
7. Cobalamin metabolism and the clinical application in its different forms Page:716—720
8. Study progress on application of aromatase inhibitors on short stature in adolescent boys Page:712—715
9. Contrastive study of three different treatments of unstable distal ulna and radius fractures in older children Page:705—708
10. Analysis of clinical phenotype and genotype in patients with 21-hydroxylase deficiency in Hunan Page:686—690
11. Multi-disciplinary interventions for the management and prevention of methylmalonic academia Page:647—652
12. Attention is paid to exclusion of genetic-metabolic liver disease in diagnosis of childhood drug-induced liver injury Page:653—655
13. Mutation analysis of patients with 6-pyruvoyltetrahydropterin synthase deficiency in Henan Page:691—694
14. Inherited metabolic disorders and intellectual disability Page:656—661
15. Correlation analysis of T lymphocyte subsets and cytokines with hepatitis B virus-associated-glomerulonephritis in children Page:700—704