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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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8
Volume:
33
Issue:
8
1. Research advances in etiology of pituitary stalk interruption syndrome
Page:561—564
2. Clinical features of pituitary stalk interruption syndrome in neonates and infants
Page:565—568
3. Clinical and imaging characteristics and treatment follow-up of pituitary stalk interruption syndrome in children
Page:569—571
4. Analysis of types and metabolic profiles of hyperphenylalaninemia
Page:572—575
5. Correlation of genotype, phenotype and treatment efficacy of Diamond-Blackfan anemia
Page:576—579
6. CT imaging features and its correlation with histopathology of thyroid nodules in children
Page:580—584
7. Study on GLIS3 mutations in children with congenital hypothyroidism
Page:585—588
8. Genetic diagnosis of erythrocyte pyruvate kinase deficiency and discovery of PKLR gene novel mutations
Page:589—592
9. Four years clinical follow-up and review analysis in a novel IBA57 mutation associated multiple mitochondrial dysfunction syndrome
Page:593—597
10. Analysis of diagnosis and treatment of solid pseudopapillary neoplasm of pancreas in 12 children
Page:598—601
11. Study on gene mutation in benign familial neonatal epilepsy
Page:602—606
12. Clinical characteristics and risk factors of post-traumatic seizures in children
Page:607—610
13. Clinical efficacy of Flunarizine in treating alternating hemiplegia in children and the influencing factors
Page:611—614
14. Analysis of SLC25A13 gene mutations in neonatal intrahepatic cholestasis caused by Citrin deficiency
Page:615—617
15. Two cases of 17β-hydroxysteroid dehydrogenase 3 deficiency and literature review
Page:618—620
16. Chromosome microarray analysis of 3 patients with different phenotypes of DiGeorge syndrome
Page:620—622
17. Clinical analysis of 10 cases with fetal neuroblastoma
Page:623—624
18. A novel mutation causes autosomal recessive pseudohypoaldosteronism type Ⅰ
Page:625—626
19. Case report of rare phenotype in type C Niemann-Pick disease
Page:627—629
20. A infantile patient with 3p deletion syndrome
Page:629—630
21. Advances in the radioactive iodine treatment for pediatric differentiated thyroid cancer
Page:631—634
22. Advances on the research of 3-hydroxy-3-methylglutaric aciduria
Page:635—637
23. Research progress in diagnosis and treatment of female heterozygotes with X-linked adrenoleukodystrophy
Page:638—640