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凝血因子Ⅻ缺乏症一例 被引量:2

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出处 《中华检验医学杂志》 CAS CSCD 北大核心 2004年第10期662-662,共1页 Chinese Journal of Laboratory Medicine
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  • 1Ronald Hoffman,Edward J,Benz Jr, et al. Hematology Basic Principles and Practice3rd Edition.Beijing:Harcourt Asia Churchill Livingstone,2001,1912-1924. 被引量:2
  • 2Cool DE,Macgillivray RTA. Characterization of the human blood coagulation factor Ⅻ gene. J Bio Chem,1987,262:13662-13673. 被引量:2
  • 3Lammle B, Wailleman WA, Huber I, et al. Thromboembolism and bleeding tendency in congenital FXII deficiency-a study on 74 subjects form 14 Swiss families. Thromb Haemost, 1991,65:117. 被引量:2

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同被引文献16

  • 1彭丽晨.脑血通对实验大鼠血液流变性及凝血功能的改变[J].中国血液流变学杂志,2004,14(4):563-564. 被引量:2
  • 2朱文艳,高华强,邹嘉平.凝血因子Ⅻ缺乏一例[J].江苏医药,2005,31(2):118-118. 被引量:2
  • 3陈燕,陈忠明,杨光辉,李雪梅,王丽颖,王惠萱.PT.APTT.TT手工法与凝血仪法对比分析在临床中的应用[J].医疗装备,2005,18(6):38-39. 被引量:3
  • 4王学锋,戴菁,王明山,丁秋兰,王鸿利.两个遗传性凝血因子Ⅻ缺陷症家系FⅫ基因突变分析[J].诊断学理论与实践,2005,4(6):447-450. 被引量:12
  • 5Kanaji T, Kanaji S, Osaki K, et al. Identification and characteriza- tion of two novel mutation (Q421K and R123P) in congenital fac- tor Ⅻ deficiency. Thromb Haemost ,2001,86(6) : 1409-1415. 被引量:1
  • 6McMullen BA, Fujikawa K. Amino acid sequence of the heavy chain of human a-factor Ⅻa( activated Hageman factor). J Biol Chem, 1985,260 (9) :5328-5341. 被引量:1
  • 7Sofia JM, Almasy L, Souto JC, ct al. A Quantitative-trait locus in the human factor Ⅻ hehe influences both plasma factor Ⅻ levels and susceptibility to thrombotic disease. Am J Hum Genet,2002, 70(3) :567-574. 被引量:1
  • 8Colhoun HM, Zito F, Chan NN, et al. Activated factor Ⅻ levels and factor Ⅻ 46C/T genotype in relation to coronary artery calcification in patients with type 1 diabetes and healthy subjects. Atherosclero- sis,2002,163 (2) :363-369. 被引量:1
  • 9Kanaji T, Okamura T, Osaki K, et al. Common genetic polymor- phism(46C to T substitution) in the 5'-untranslated region of the coagulation factor Ⅻ gene is associated with low translation effi- ciency and decrease in plasma factor Ⅻ level. Blood, 1998,91 (6) :2010-2014. 被引量:1
  • 10Zito F, Lowe GD, Rumley A, et al. Association of the factor Ⅻ 46C > T polymorphism with risk of coronary heart disease (CHD) in the WOSCOPS stugy. Atherosclerosis ,2002,165 : 153. 被引量:1

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