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积极开展遗传代谢病的临床研究 被引量:2

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作者 秦炯
出处 《中国医刊》 CAS 2006年第3期2-3,共2页 Chinese Journal of Medicine
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同被引文献12

  • 1顾学范,韩连书,高晓岚,杨艳玲,叶军,邱文娟.串联质谱技术在遗传性代谢病高危儿童筛查中的初步应用[J].中华儿科杂志,2004,42(6):401-404. 被引量:142
  • 2韩连书,高晓岚,叶军,邱文娟,顾学范.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):325-330. 被引量:62
  • 3杨艳玲.遗传代谢病的诊断与治疗[J].国外医学(内分泌学分册),2005,25(4):238-240. 被引量:19
  • 4Arthur LB,Charles RS,William SS,et al.Genetics,biochemistry,and molecular basis of variant human phenotypes.The metabolic and molecular bases of inherited disease.7th ed.McGraw:Hill,1995:53-118.
  • 5Cleary M,Green A.Developmental delay:when to suspect and how to investigate for an inborn error of metabolism.Arch Dis Child,2005,90(11):1128-1132.
  • 6Enns GM.Inborn errors of metabolism masquerading as hypoxic-ischemic encephalopathy.NeoReviews,2005,6 (12):549-558.
  • 7Chakrapani A,Cleary MA,Wraith JE.Detection of inborn errors of metabolism in the newborn.Arch Dis Child Fetal Neonatal,2001,84(3):205-210.
  • 8Burton BK.Inborn errors of metabolism in infancy:A guide to diagnosis.J Pediatr,1998,102(6):69.
  • 9Raghuveer TS,Garg U,Graf WD.Inborn errors of metabolism in infancy and early childhood:An update.Am Fam Physician,2006,73(11):1981-1990.
  • 10Arbeiter AK,Kranz B,Wingen AM,et al.Continuous venovenous haemodialysis (CVVHD) and continuous peritoneal dialysis (CPD) in the acute management of 21 children with inbom errors of metabolism.Nephrol Dial Transplant,2010,25(4):1257-1265.

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