Volume: 35 Issue: 20

1. Growth profile of children with common type disorders of sex development Page:1594—1597
2. Introduction of recommendations on the diagnosis and management of steroid-resistant nephrotic syndrome in children proposed by the International Pediatric Nephrology Association Page:1531—1540
3. Research advances in the role of ion channels genetics in autism spectrum disorders Page:1597—1600
4. The nutritional management of hepatic glycogen storage diseases Page:1546—1548
5. Analysis of clinical characteristics and related gene mutation characteristics in a case of maple syrup urine disease Page:1586—1588
6. Behavioral problems of children with congenital adrenal hyperplasia and their influencing factors Page:1561—1565
7. Discussion on the principle of protein restriction in the acute stage of hereditary metabolic diseases from the perspective of acrodermatitis with metabolic disorders Page:1541—1545
8. Compound heterozygous mutations of Fanc A gene in two children with Fanconi anemia Page:1588—1590
9. The changes and clinical significance of serum bilirubin in children with type 1 diabetes mellitus Page:1557—1560
10. The diagnostic value of the basal luteinizing hormone level for girls with central precocious puberty based on body mass index Page:1566—1570
11. A family with creatine deficiency syndrome due to SLC6A8 gene novel mutation Page:1591—1593
12. Long-term nutritional management of inherited metabolic disorders with hypoglycemia Page:1549—1552
13. Application of chromosome microarray analysis in congenital heart disease in infants and young children Page:1577—1582
14. Long term follow-up and efficacy of continuous subcutaneous insulin infusion in the treatment of children with type 1 diabetes mellitus in Qingdao Page:1553—1556
15. Erythema multiforme caused by Mycoplasma pneumoniae infection in 3 children Page:1583—1585
16. Analysis of the effect of the simultaneous combined operation for congenital heart disease complicated with non-cardiac malformation Page:1571—1576