Article List

WPRIM Management System> DCMS> Chinese Journal of Pediatrics> 2013> 51> 3

Volume: 51 Issue: 3

1. WHIM syndrome: a case report and literature review.	Page:178—182
2. Progress of ATP-binding cassette transporter A3 gene and respiratory diseases of children.	Page:234—236
3. Advances in minimal residual disease detection with flow cytometry in childhood acute myeloid leukemia.	Page:231—234
4. Progresses in characteristics and diagnostic methods of neonatal diffuse intravascular coagulation.	Page:227—230
5. Lung ultrasonography for the diagnosis of neonatal respiratory distress syndrome: a pilot study.	Page:205—210
6. Clinical study of variation and significance of the high insulin levels in critically ill children.	Page:199—204
7. Effect of food allergy early in life on visceral hyperalgesia in the developing rats and role of substance P abnormal expression in colon.	Page:172—177
8. Cohort study of 684 pairs of mother-and-child allergic diseases.	Page:168—171
9. A case of congenital subglottic hemangiomas.	Page:239—240
10. Typical WAGR syndrome in a case.	Page:237—239
11. Chest CT features and outcome of necrotizing pneumonia caused by Mycoplasma pneumoniae in children (report of 30 cases).	Page:211—215
12. Outcomes of patients with combined methylmalonic acidemia and homocystinuria after treatment.	Page:194—198
13. Reading and interpreting the CPA-AIR recommendations for the diagnosis and management of juvenile systemic iupus erythematosus (continued).	Page:189—193
14. Reading and interpreting evidence based recommendations for the diagnosis and management of cow's milk allergy in Chinese infants.	Page:187—188
15. Issues to address in developing evidence based clinical practice guidelines: experience from evidence-based recommendations for the diagnosis and treatment of cow's milk protein allergy in infants.	Page:165—167
16. Progress in treatment of systemic lupus erythematosus.	Page:161—164
17. Amplitude-integrated electroencephalographic changes in neonates with acute bilirubin encephalopathy.	Page:221—226
18. Analysis of clinical and genetic characteristics of 20 cases of children with Silver Russell syndrome.	Page:216—220