WPRIM Management System> DCMS> Journal of Clinical Pediatrics> 2017> 35> 8

Volume: 35 Issue: 8

1. Progress on genetics and therapy in the spinal muscular atrophy Page:632—635
2. Effects of gross hematuria on the results in laboratory urine examination Page:629—631,640
3. Application of next generation sequencing technology for genetic diagnosis of a case with globoid cell leukodystrophy Page:625—628
4. IPEX with congenital ichthyosiform skin lesions:a case report and literature review Page:620—624
5. Gene mutation associated with hemophagocytic lymphohistiocytosis in children Page:616—619
6. Clinical features and PHKG2 gene mutation analysis of 5 Chinese patients with glycogen storage disease Ⅸc Page:609—612
7. The clinical and genetic features of holocarboxylase synthetase deficiency in a male patient Page:605—608
8. A de novo mutation in GNAS cause severe pseudohypoparathyroidism typeⅠa Page:601—604
9. Analysis on epidemiology and clinical characteristics of 3431 pediatric patients with measles Page:589—591
10. Clinical characteristics and etiological analysis of lung nodules in 98 children Page:585—588
11. Clinical features of bronchiectasis in 182 children in Chongqing with etiology analysis Page:580—584
12. Clinical characteristics and risk factors of refractory Mycoplasma pneumoniae pneumonia in children Page:569—574
13. Effect of sublingual immunotherapy on the balance of Th17/Treg for children with mite, allergic asthma Page:565—568
14. The characteristics of tidal breath lung function and growth level among infants with recurrent wheezing Page:561—564
15. One case report of Jacobsen syndrome combine with Paris-Trousseau syndrome Page:613—615
16. Siblings with congenital adrenal cortex hyperplasia (17-α-hydroxylase deficiency) and literature review Page:597—600
17. Clinical significance of serum interleukin-1β and interleukin-6 levels in childhood hyperuricemia Page:592—596
18. Value of combining PCT, BNP, D-dimer and PCIS score in predicting the prognosis of severe pediatric pneu-monia Page:575—579

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