期刊文献+

浅谈儿科传染病发热时降温措施选择 被引量:2

下载PDF
导出
摘要 发热即是体温异常升高,也是机体疾病反应的最常见信号,其发热特点:常有一定的热型及自然热程。探讨发热时常见病因及发热时的机体生理变化及处理方法,充分认识发热的概念及发病机制,耐心做通儿童家长工作,正确对待、处理发热。
作者 刘桂苹
出处 《中国实用医药》 2011年第2期223-224,共2页 China Practical Medicine
  • 相关文献

参考文献4

二级参考文献32

  • 1CasteelsVanDaele M, Wouters C, VanGeet C, et al. Reye-syndrome revisited:a descriptive term covering a group of heterogenous disorders. Eur J Pediatr, 2000, 159:641 - 648.
  • 2Glasgow JFT, Middleton B. Reye-syndrome:insights on causation and grognosis. Arch Dis Child, 2001, 85:351 - 353.
  • 3Hardie RM, Newton LH, Bruce JC, et al. The changing clinical pattern of reye's syndrome. Arch Dis Child, 1996, 74:400.
  • 4Voekey J, Whiteman DA. Defects of mitochondrial β-oxidation :a growing group of disorders. Neuromuscul Disord, 2002, 12:235 - 246.
  • 5Tyni T, Pihko H. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Acta Paediatr, 1999, 88 : 237 - 245.
  • 6Bzduch V, Behulova D, Lehnert W, et al. Metabolic cause of reye-like syndrome. Bratisl Lek Listy, 2001, 102:427 - 429.
  • 7He M, Rutledge SL, Kelly DR, et al. A new genetic disorder in mitochondrial fatty acid β- oxidation :ACAD9 deficiency. Am J Hum Genet, 2007, 81:87 - 103.
  • 8Bennett MJ, Russell LK, Tokunaga C, et al. Reye-like syndrome resulting from novel missense mutations in mitochondrial medium-and short-chain 1-3-hydroxy-acyl-CoA dehydrogenase. Mol Genet Metab, 2006, 89:74 - 79.
  • 9Sauer SW, Okun JG, Hoffmann GF, et al. Impact of short- and medium-chain organic acids, acylcarnitines, and acyl-CoAs onmitochondrial energy metabolism. Biochim Biophys Acta, 2008, 10:1276 - 1282.
  • 10Lemaster JJ, Nieminen AL, Qian T, et al. The mitochondrial permeability transition in toxic, hypoxic and reperfusion injury. Mol Cell Biochem, 1997, 174:159- 165.

共引文献23

同被引文献16

引证文献2

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部