Article List

WPRIM Management System> DCMS> Chinese Journal of Pediatrics> 2014> 52> 11

Volume: 52 Issue: 11

1. BCR-ABL T315I mutant acute lymphoblastic leukemia in 3 children.	Page:876—878
2. Analysis of two cases with idiopathic infantile arterial calcification.	Page:874—876
3. Report of a case with severe hand, foot mouth disease and acute necrotizing enterocolitis.	Page:872—873
4. Maturity-onset diabetes of the young 2 with a novel mutation of glucokinase gene in a Chinese boy and the clinical follow-up.	Page:867—871
5. Clinical features of pyruvate dehydrogenase complex deficiency and gene testing in one case.	Page:863—866
6. Relationship between hyperuricemia and primary nephrotic syndrome in children.	Page:859—862
7. Experience in diagnosis and treatment of asparaginase-associated pancreatitis in children.	Page:854—858
8. Diagnosis of children with occult bronchial foreign body.	Page:851—853
9. I73T mutation in the pulmonary surfactant protein C gene associated with pediatric interstitial lung disease: a case study and the review of related literature.	Page:846—850
10. Effect of DNA methylation on the proliferation of leukemia cells regulated by miR-34b.	Page:840—845
11. Neurocognitive and behavioral functioning in children with sleep- disordered breathing.	Page:836—839
12. Diagnosis and treatment of Fanconi anemia.	Page:833—835
13. Progress in respiratory function assessment and management for Duchenne muscular dystrophy.	Page:831—832
14. Progress of sudden unexpected death in epilepsy.	Page:828—830
15. Clinical and genetic analysis of a family with Aicardi-Goutières syndrome and literature review.	Page:822—827
16. SUCLA2-related encephalomyopathic mitochondrial DNA depletion syndrome: a case report and review of literature.	Page:817—821
17. Efficacy and safety of rapamycin in treatment of children with epilepsy complicated with tuberous sclerosis.	Page:812—816
18. Phenotypes and PRRT2 mutation analysis in families with benign familial infantile epilepsy.	Page:806—811
19. Rare diseases need efforts of medical workers, let our love be not rare.	Page:804—805
20. Reasonable use of new technology to detect genetic disease, improve the level of diagnosis and treatment of pediatric nervous system diseases.	Page:801—803