Volume: 31 Issue: 20

1. Paying more attention to the prevention and treatment of maternal phenylketonuria Page:1521—1524
2. Medical treatment of peripheral precocious puberty Page:1591—1594
3. Study progress of autoimmune hepatitis in children Page:1598—1600
4. Clinical significance of monitoring bone turnover markers changes before and after growth hormone treatment of prepubertal children with idiopathic short stature Page:1541—1545
5. The molecular diagnosis and their detailed clinical presentations in 5 cases of maturity-onset diabetes of the young Page:1546—1549
6. Multiplex ligation-dependent probe amplification gene detection for diagnosis of 3 patients with Prader-Willi syndrome Page:1580—1581
7. Study of copy number variations in children with unexplained mental retardation/brain development delay Page:1550—1555
8. Clinical analysis of inherited metabolic diseases in the neonatal intensive care unit Page:1556—1558
9. Analysis of epidemic characteristics and clinical features of inpatients with pertussis in 2012-2014 Page:1559—1562
10. Effect of lipopolysaccharide-mediated infection during pregnancy on the expression of mineralocorticoid receptor and dendritic spines in hippocampus of rat offspring Page:1567—1570
11. Gene mutation detection of one patient with pyruvate dehydrogenase complex deficiency by using next generation sequencing Page:1575—1577
12. Clinical analysis of Prader-Willi syndrome in 10 children Page:1578—1579
13. Efficacy of recombinant human erythropoietin combined with exogenous single sialic acid four hexose ganglioside in treatment of median-severe neonatal hypoxic-ischemic encephalopathy Page:1582—1583
14. Two cases of Apert syndrome Page:1584—1585
15. A infantile Guillain-Barré syndrome less than 3-month-old Page:1586—1587
16. Research progress of changes in thyroid function in short stature children both before and after therapy Page:1595—1597