Article List

WPRIM Management System> DCMS> Journal of Clinical Pediatrics> 2018> 36> 2

1. Determination of Clara cell secretory protein 16 and pulmonary surfactant protein D in children with severe pneumonia and its clinical significance	Page:81—86
2. Genome-wide copy number variations in congenital cystic lung disease	Page:87—90
3. Clinical features of three pulmonary alveolar proteinosis patients	Page:91—94
4. Prospective study on the relationship between CCL22, a cord blood chemokine, and risk of atopic diseases	Page:108—112
5. Association between polymorphism of NDUT15 gene and leucopenia induced by 6-mercaptopurine in children with acute lymphoblastic leukemia	Page:113—116
6. Analysis of clinical phenotype and genetic diagnosis in patients with Omenn syndrome	Page:117—120
7. Neonatal inflammatory bowel disease: a report of 2 cases with literature review	Page:121—125
8. Clinical investigation of aortopulmonary collateral arteries	Page:126—130
9. Acute myelitis with positive GM1 antibodies in children: a report of two cases	Page:131—133
10. Clinical and genetic analysis in a patient with type 4 Aicardi-Goutières syndrome	Page:134—137
11. Hexokinase deficiency: a case report with literature review	Page:138—141
12. Clinical features and mutation of STK11 gene in four patients with Peutz-Jeghers syndrome	Page:142—144,160
13. Research progress on community-acquired respiratory distress syndrome toxin	Page:145—148
14. Progress on minimal residual diseases in childhood solid tumor	Page:149—154