Volume: 30 Issue: 24

1. Hippocampal neuronal damage and its possible mechanism in status epilepticus Page:1855—1858
2. Significance of arylsulfatase A gene detection for the diagnosis of metachromatic leukodystrophy Page:1859—1862
3. Clinical and OTC gene mutation analysis of one child with ornithine transcarbamylase deficiency Page:1905—1907
4. Levetiracetam treatment for neonatal intractable seizure Page:1912—1914
5. Advances in the genetic mechanism of tuberous sclerosis complex Page:1841—1844
6. Clinical analysis of 113 cases of tuberculous pleurisy in children Page:1891—1893
7. Distribution of common chromosomal karyotypes in patients with Turner syndrome and correlation between the mean age and height standard deviation scores on diagnosis Page:1894—1897
8. Meta analysis of the alarm treatment and desmopressin in the treatment of primary nocturnal enuresis in children Page:1898—1904
9. Phosphatidylinositol 3-kinase/protein kinase B/mammalian target of rapamycin signaling pathway and epilepsy Page:1915—1917
10. The utility of BTBR mouse model in autism research Page:1918—1920
11. Clinical characteristics and diagnosis progress in tuberous sclerosis complex Page:1845—1847
12. Surveillance and management of tuberous sclerosis complex Page:1847—1850
13. Surgical treatment of epilepsy in tuberous sclerosis complex Page:1851—1854
14. Clinical and imaging characteristics of posterior reversible encephalopathy syndrome in children with acute lymphoblastic leukemia after chemotherapy induction Page:1863—1867
15. Application of magnetic resonance diffusion tensor imaging technology in neonates with hypoxic-ischemic encephalopathy in the subacute stage Page:1868—1872
16. Infantile spinal muscular atrophy in 39 children Page:1873—1876
17. The sleep structure of children with attention deficit hyperactivity disorder Page:1877—1879
18. Clinical effects of auditory integrative training on children with spastic cerebral palsy Page:1880—1882