Article List

WPRIM Management System> DCMS> Chinese Journal of Pediatrics> 2014> 52> 6

Volume: 52 Issue: 6

1. Reviews of the Twentieth International Congress of Nutrition.	Page:479—480
2. Anomalous origin of right pulmonary artery from the aorta and patent ductus arteriosus in a case.	Page:477—478
3. Primary pulmonary rhabdomyosarcoma in children: report of 1 case.	Page:475—476
4. Neonatal pulmonary artery sling with pneumonia as the first manifestation after birth: report of one case.	Page:473—474
5. Cardiac catheterization and pulmonary vasoreactivity testing in children with idiopathic pulmonary arterial hypertension.	Page:468—472
6. Prenatal factors associated with high BMI status of infants and toddlers.	Page:464—467
7. Analysis of genomic copy number variations in two unrelated neonates with 8p deletion and duplication associated with congenital heart disease.	Page:460—463
8. A family with two children diagnosed with aspartylglucosaminuria-case report and literature review.	Page:455—459
9. Treatment outcome of childhood standard-risk and median-risk acute lymphoblastic leukemia with CCLG-2008 protocol.	Page:449—454
10. Human parechovirus associated sepsis and central nervous system infections in hospitalized children.	Page:444—448
11. A multicenter prospective clinical study on continuous blood purification in treating childhood severe sepsis.	Page:438—443
12. Clinical application of blood purification (artificial liver) in treatment of acute liver failure in children.	Page:433—437
13. Interpretation of the consensus about the diagnosis and treatment of hyperphenylalaninemia.	Page:430—432
14. Treatment recommendations for invasive fungal disease in pediatric patients with cancer or blood disease.	Page:426—429
15. Consensus about the diagnosis and treatment of hyperphenylalaninemia.	Page:420—425
16. Clinical and laboratory studies on 28 patients with glutaric aciduria type 1.	Page:415—419
17. Follow up and gene mutation analysis in cases suspected as 3-methylcrotonyl-coenzyme A carboxylase deficiency by neonatal screening.	Page:409—414
18. Analysis of clinical features and arylsulfatase B gene mutation in thirteen Chinese children with mucopolysaccharidosis type VI.	Page:403—408
19. Reinforcement of the diagnosis and treatment of hyperphenylalaninemia and prognostic study.	Page:401—402