Article List

WPRIM Management System> DCMS> Chinese Journal of Pediatrics> 2014> 52> 12

Volume: 52 Issue: 12

1. Measles pneumonitis in pediatric liver transplant recipients-case report.	Page:952—953
2. A novel homozygous mutation p.E25X in the HSD3B2 gene causing salt wasting 3β-hydroxysteroid dehydrogenases deficiency in a Chinese pubertal girl: a delayed diagnosis until recurrent ovary cysts.	Page:948—951
3. Children with idiopathic hypogonadotropic hypogonadism: clinical data analysis and mutations analysis of KAL1 and FGFR1 gene.	Page:942—947
4. Diagnosis of MECP2 duplication syndrome with molecular genetic techniques.	Page:937—941
5. Report of a child with neonatal-onset multisystem inflammatory disease and review of the literature.	Page:932—936
6. Role of Th17/Treg imbalance in the immune pathogenesis and treatment of children with aplastic anemia.	Page:927—931
7. A case of autoimmune lymphoproliferactive syndrome and literature review.	Page:923—926
8. Central venous-to-arterial carbon dioxide difference in critically ill pediatric patients with septic shock.	Page:918—922
9. Thinking of bronchopulmonary dysplasia from "classic" to the "new" transformation.	Page:909—912
10. Clinical advance of atypical severe combined immunodeficiency.	Page:906—909
11. Clinical characteristics of children with Langerhans cell histiocytosis with pulmonary involvement.	Page:902—905
12. Mutations of NOD2 gene and clinical features in Chinese Blau syndrome patients.	Page:896—901
13. Clinical characteristics and treatment responses of X-linked thrombocytopenia.	Page:890—895
14. New interpretation of autoinflammatory diseases.	Page:885—889
15. Primary immunodeficiency diseases: challenges and opportunities for Chinese pediatrician.	Page:881—884