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促红细胞生成素在缺氧缺血性脑损伤新生兔中的表达 被引量:5

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出处 《中华妇幼临床医学杂志(电子版)》 CAS 2010年第3期207-209,共3页 Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition)
基金 福建省教育厅基金(JB07203) 泉州市科技局基金项目(2007Z50)
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  • 1姚裕家.新生儿缺氧缺血性脑病的临床诊断[J].中华妇幼临床医学杂志(电子版),2005,1(1):7-7. 被引量:3
  • 2Robinson SM,Barker DJ.Coronary heart disease:A disorder of growth[J].Proc Nutr Soc,2002,61(2):537-542.
  • 3林迳苍,朱世泽,杜翠琼,许相洋,黄煌.ICAM-1及VCAM-1等在HIE新生兔的表达[J].重庆医科大学学报,2008,33(12):1499-1501. 被引量:2
  • 4Ruscher K,Freyer D,Karsch M,et al.Erythropoietin is a paracrine mediatorof ischemic tolerance in the brain:Eevidence from an in vitro model[J].J Neurosci,2002,22(23):10291.
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同被引文献42

  • 1孙喜斌,李兴启,张华.中国第二次残疾人抽样调查听力残疾标准介绍[J].听力学及言语疾病杂志,2006,14(6):447-448. 被引量:69
  • 2Ciuman RR. Inner ear symptoms and disease: pathophysiological understanding and therapeutic options[J]. Med Sci Monit, 2013, 19:1195-1210.
  • 3Ohgami N,Iida M,Yajima I,et al. Hearing impairments caused by genetic and environmental factors[J]. Environ Health Prey Med, 2013,18(1) : 10-15.
  • 4Wang Z, Huang Z, Lu G,et al. Hypoxia during pregnancy in rats leads to early morphological changes of atherosclerosis in adult offspringE J]. Am J Physiol Heart Circ Physiol, 2009, 296 ( 5 ) : H1321-HI328.
  • 5Giussani DA, Riquelme RA, Moraga FA,et al. Chemoreflex and endocrine components of cardiovascular responses to acute hypoxemia in the llama fetus[J]. Am J Physiol,1996,271(1 Pt 2) : R73-R83.
  • 6Stein LK. Factors influencing the efficacy of universal newborn bearing screening[J]. Pediatr Clin North Am, 1999,46( l ) : 95-105.
  • 7Shibata SB,Raphael Y. Future approaches for inner ear protectionand repair[J]. J Commun Disord,2010,43(4) :295-310.
  • 8Vohr PR, Widen JE, Cone-Wesson B, et al. Identification of neonatal hearing impairment: characteristics of infants in the neonatal intensive care unit and well-baby nursery[J]. Ear Hear, 2000,21(5) :373-382.
  • 9Ambrosi C, Boassa D, Pranskevich J, et al. Analysis of four connexin26 mutant gap junctions and hemichannels reveals variations in hexamer stabillty[J]. Biophys J, 2010, 98 (9) : 1809- 1819.
  • 10Chen G, I.iu J,Dong J,et al. GJB2 mutations are rare in probands with hearing loss in Chinese assortative mating families[J]. Int J Pediatr Otorhinolaryngol, 2014,78(2) : 244-247.

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