Article List

WPRIM Management System> DCMS> Journal of Clinical Pediatrics> 2017> 35> 11

Volume: 35 Issue: 11

1. Impact of factors to delayed diagnosis and its clinical outcome on Guillain-Barré syndrome	Page:801—805
2. The clinical and genetic features of a case with antenatal form of leukoencephalopathy with vanishing white matter disease	Page:806—809
3. A case of SUCLG1-related infantile encephalomyopathy mitochondrial DNA depletion syndrome	Page:810—814
4. A case of Cockayne syndrome caused by ERCC8 gene mutation	Page:815—819
5. A homozygous mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy: a case report	Page:820—822,825
6. Clinical value of active electroencephalography in attention-deficit hyperactivity disorder	Page:823—825
7. Effects of a GOS+FOS supplemented formula on stool characteristics and fecal beneficial bacteria content in infants	Page:826—831
8. Analysis of correlation between immunosuppression and organ dysfunction in children with sepsis	Page:832—836
9. Clinical and radiological manifestations of 5 pediatric cases with cystic fibrosis	Page:837—840
10. A case report of cerebrotendinous xanthomatosis with novel mutations in CYP27A1 gene	Page:841—843
11. Juvenile-onset clinically amyopathic dermatomyositis complicated with progressive interstitial pneumonia: report of one case and review of the literature	Page:844—847,851
12. Clinical features of Diamond-Blackfan anemia and gene testing	Page:848—851
13. Analysis of influence factors on anemia in preterm infants	Page:852—856
14. Clinical analysis of 8 cases of neonatal hand-foot-mouth disease	Page:857—859
15. Analysis of diagnosis and treatment of childhood colonic polyps	Page:860—863
16. Genetic studies in early infantile epileptic encephalopathy	Page:864—867
17. Advances in insulin-like growth factor-1 in hypoxic-ischemic encephalopathy	Page:868—872
18. Investigation on tigecycline therapy for severe infections in children	Page:873—876,880