幼儿异戊酸血症的临床特征分析(3)
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[11]Sarafoglou K,Gaviglio A,Hietala A,et al.Comparison of newborn screening protocols for congenital adrenal hyperplasia in preterm infants[J].J Pediatr,2014,164(5):1136-1140.
[12]Sharma R,Seth A.Congenital adrenal hyperplasia:issues in diagnosis and treatment in children[J].Indian J Pediatr,2014,81(2):178-185.
[13]楊艳玲.有机酸代谢病的高危筛检[J].继续医学教育,2006,20(17):35-39.
[14]Singh RH,Rohr F,Frazie RD,et al.Recommendations for the nutrition management of phenylalanine hydroxylase deficiency[J].Genet Med,2014,16(2):121-131.
(收稿日期:2016-08-11 本文编辑:方菊花) (王仙 王正洪 商杰)
[8]任常军,李彦敏,陈宝昌,等.异戊酸血症1例报告[J].临床儿科杂志,2009,27(12):1285.
[9]韩连书,高晓岚,叶军,等.串联质谱技术在有机酸血症筛查中的应用研究[J].中华儿科杂志,2005,43(5):167-180.
[10]Ribeiro CA,Leipnitz G,Amaral AU,et al.Creatine administration prevents Na+-K+-ATP ase inhibition induced by intracerebroventricular administration of isovaleric acid in cerebral cortex of young rats[J].Brain Res,2009,1262:81-88.
[11]Sarafoglou K,Gaviglio A,Hietala A,et al.Comparison of newborn screening protocols for congenital adrenal hyperplasia in preterm infants[J].J Pediatr,2014,164(5):1136-1140.
[12]Sharma R,Seth A.Congenital adrenal hyperplasia:issues in diagnosis and treatment in children[J].Indian J Pediatr,2014,81(2):178-185.
[13]楊艳玲.有机酸代谢病的高危筛检[J].继续医学教育,2006,20(17):35-39.
[14]Singh RH,Rohr F,Frazie RD,et al.Recommendations for the nutrition management of phenylalanine hydroxylase deficiency[J].Genet Med,2014,16(2):121-131.
(收稿日期:2016-08-11 本文编辑:方菊花) (王仙 王正洪 商杰)