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WPRIM Management System>
DCMS
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Chinese Journal of Applied Clinical Pediatrics
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2018
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33
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4
Volume:
33
Issue:
4
1. Focus on monogenic disorders in respiratory apparatus in children
Page:247—249
2. Combined immunodeficiency
Page:250—256
3. Activated phosphoinositide 3-kinase δ syndrome
Page:256—259
4. Mendelian susceptibility to mycobacterial disease
Page:259—264
5. Gain-of-function signal transducer and activator of transcription 1 deficiency
Page:264—267
6. Genetic defect types associated with interstitial lung disease
Page:267—272
7. Progress of diagnosis and treatment of congenital central hypoventilation syndrome
Page:273—276
8. Hyper-immunoglobulin E syndrome
Page:277—280
9. X-linked immunodeficiency with hyper-immunoglobulin M
Page:280—282
10. Alpha-1-antitrypsin deficiency
Page:282—285
11. 22q11.2 deletion syndrome
Page:285—288
12. X-linked agammaglobulinemia in children
Page:288—291
13. Congenital defects of phagocyte number or function
Page:291—297
14. Wiskott-Aldrich syndrome related diseases
Page:297—299
15. Study on genetic mutation of surfactant dysfunction in children with interstitial lung disease
Page:300—305
16. Primary ciliary dyskinesia in children
Page:306—308
17. Take care of children with cystic fibrosis
Page:309—312
18. Inherited neuromuscular disorders presented initially or mainly with respiratory manifestation
Page:313—316
19. Pediatric pulmonary alveolar proteinosis
Page:317—320