Article List

WPRIM Management System> DCMS> Chinese Journal of Applied Clinical Pediatrics> 2019> 34> 20

Volume: 34 Issue: 20

1. Clinical application of modern genetic analysis technology	Page:1521—1525
2. Clinical application of modern genetic analysis technology	Page:1521—1525
3. New advances in diagnosis and treatment of 21-hydroxylase deficiency	Page:1526—1530
4. Screening, diagnosis and treatment of propionic acidemia	Page:1531—1534
5. Glucose monitoring for diabetes in children	Page:1534—1536
6. Promoting the mode of individualized comprehensive management for childhood diabetes	Page:1536—1540
7. Tandem mass spectrometry screening of 565 182 newborns for inherited metabolic diseases in Hunan province	Page:1541—1545
8. DUOX2 hotspots variants and outcomes of patients with congenital hypothyroidism suspected thyroid dyshormonogenesis	Page:1546—1549
9. Large-single scale mitochondrial DNA deletions in different tissues in Kearns-Sayre syndrome	Page:1550—1554
10. Analysis of clinical and electroencephalogram characteristics of ring chromosome 14 syndrome	Page:1555—1559
11. Diagnosis and long-term follow-up of 4-hydroxy butyrate aciduria in 9 cases	Page:1560—1564
12. Study on urine metabolomics of left-behind children with vitamin D deficiency under 1 year old in Zunyi area based on nuclear magnetic resonance	Page:1565—1569
13. Analysis of neonatal deaths in critical neonatal treatment centers at different levels in Henan province	Page:1570—1575
14. Clinical efficacy of percutaneous nephrolithotomy with all-seeing needle system in treatment of upper urinary calculi in children	Page:1576—1578
15. Neurophysiological characteristics of acute inflammatory demyelinating polyneuropathies in children	Page:1579—1581
16. Correlation between the risk of migraine and metabolic syndrome in children	Page:1581—1584
17. Thoracolumbar spinal cord injury without fracture and dislocation in children :2 cases report	Page:1585—1586
18. Research progress on phenotype and mechanism of cardiac disease caused by CACNA1C gene mutations	Page:1587—1590
19. Development of individualized treatment for congenital ovarian dysplasia syndrome	Page:1591—1594
20. Research progress in association of first thousand days in life and human health	Page:1594—1597
21. Research progress in animal model of Perthes disease	Page:1598—1600
22. New advances in diagnosis and treatment of 21-hydroxylase deficiency	Page:1526—1530
23. Screening, diagnosis and treatment of propionic academia	Page:1531—1534
24. Glucose monitoring for diabetes in children	Page:1534—1536
25. Promoting the mode of individualized comprehensive management for childhood diabetes	Page:1536—1540
26. Tandem mass spectrometry screening of 565 182 newborns for inherited metabolic diseases in Hunan province	Page:1541—1545
27. DUOX2 hotspots variants and outcomes of patients with congenital hypothyroidism suspected thyroid dyshormonogenesis	Page:1546—1549
28. Large-single scale mitochondrial DNA deletions in different tissues in Kearns-Sayre syndrome	Page:1550—1554
29. Analysis of clinical and electroencephalogram characteristics of ring chromosome 14 syndrome	Page:1555—1559
30. Diagnosis and long-term follow-up of 4-hydroxy butyrate aciduria in 9 cases	Page:1560—1564
31. Study on urine metabolomics of left-behind children with vitamin D deficiency under 1 year old in Zunyi area based on nuclear magnetic resonance	Page:1565—1569
32. Analysis of neonatal deaths in critical neonatal treatment centers at different levels in Henan province	Page:1570—1575
33. Clinical efficacy of percutaneous nephrolithotomy with all-seeing needle system in treatment of upper urinary calculi in children	Page:1576—1578
34. Research progress on phenotype and mechanism of cardiac disease caused by CACNA1C gene mutations	Page:1587—1590
35. Development of individualized treatment for congenital ovarian dysplasia syndrome	Page:1591—1594
36. Research progress in association of first thousand days in life and human health	Page:1594—1597
37. Research progress in animal model of Perthes disease	Page:1598—1600