WPRIM Management System> DCMS> Chinese Journal of Applied Clinical Pediatrics> 2017> 32> 8

Volume: 32 Issue: 8

1. Clinical features and genetic analysis of intellectual disability in children with epilepsy of unknown causes Page:603—606
2. A novel mutation of the androgen receptor gene causes androgen insensitivity syndrome:a case report and literature review Page:599—602
3. Clinical and genetic study of a family with cerebro-oculo-facio-skeletal syndrome Page:595—598
4. Value of serum uric acid combined with age,waist circumference and body mass index in the prediction of metabolic syndrome in obese children Page:585—590
5. Changes of thyroid autoantibodies and its relationship with dyslipidaemia in children with Turner syndrome Page:579—581
6. Update on 46,XX primary ovarian insufficiency in adolescents Page:570—573
7. Reproductive intervention for inborn errors of metabolism Page:565—569
8. Recent advances in the diagnosis and treatment of pediatric genetic cholestasis Page:561—565
9. Current diagnosis and treatment of insomnia in children and adolescents and study progress Page:637—640
10. Progress of adverse effect of routine vaccination in children with epilepsy Page:634—636
11. Progress of effects of hypothyroidism during pregnancy on the offspring Page:631—633
12. Slow weight gain and unremarkably increased urine methylmalonic acid Page:613—616
13. Case-control study on clinical features and influencing factors of children with autism spectrum disorders Page:607—612
14. Diagnosis and treatment of dyskeratosis congenita in Chinese children Page:591—594
15. Clinical characteristics and gene mutations analysis of 56 patients with congenital hyperinsulinism Page:574—578

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