Volume: 33 Issue: 8

1. Research advances in etiology of pituitary stalk interruption syndrome Page:561—564
2. Clinical features of pituitary stalk interruption syndrome in neonates and infants Page:565—568
3. Clinical and imaging characteristics and treatment follow-up of pituitary stalk interruption syndrome in children Page:569—571
4. Analysis of types and metabolic profiles of hyperphenylalaninemia Page:572—575
5. Correlation of genotype, phenotype and treatment efficacy of Diamond-Blackfan anemia Page:576—579
6. CT imaging features and its correlation with histopathology of thyroid nodules in children Page:580—584
7. Study on GLIS3 mutations in children with congenital hypothyroidism Page:585—588
8. Genetic diagnosis of erythrocyte pyruvate kinase deficiency and discovery of PKLR gene novel mutations Page:589—592
9. Four years clinical follow-up and review analysis in a novel IBA57 mutation associated multiple mitochondrial dysfunction syndrome Page:593—597
10. Analysis of diagnosis and treatment of solid pseudopapillary neoplasm of pancreas in 12 children Page:598—601
11. Study on gene mutation in benign familial neonatal epilepsy Page:602—606
12. Clinical characteristics and risk factors of post-traumatic seizures in children Page:607—610
13. Clinical efficacy of Flunarizine in treating alternating hemiplegia in children and the influencing factors Page:611—614
14. Analysis of SLC25A13 gene mutations in neonatal intrahepatic cholestasis caused by Citrin deficiency Page:615—617
15. Two cases of 17β-hydroxysteroid dehydrogenase 3 deficiency and literature review Page:618—620
16. Chromosome microarray analysis of 3 patients with different phenotypes of DiGeorge syndrome Page:620—622
17. Clinical analysis of 10 cases with fetal neuroblastoma Page:623—624
18. A novel mutation causes autosomal recessive pseudohypoaldosteronism type Ⅰ Page:625—626
19. Case report of rare phenotype in type C Niemann-Pick disease Page:627—629
20. A infantile patient with 3p deletion syndrome Page:629—630
21. Advances in the radioactive iodine treatment for pediatric differentiated thyroid cancer Page:631—634
22. Advances on the research of 3-hydroxy-3-methylglutaric aciduria Page:635—637
23. Research progress in diagnosis and treatment of female heterozygotes with X-linked adrenoleukodystrophy Page:638—640