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缓激肽与C_1抑制物缺乏症 被引量:1

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出处 《医学综述》 2005年第6期491-493,共3页 Medical Recapitulate
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  • 1Sofia S, Casali A, Bolondi L. Sonographie findings in abdominal hereditary angioedema[J] .J Clin Ultrasound, 1999,27(9):537-540.
  • 2Janson M, Larsson C, Werelius B, et al. Detailed physical map of human chromosomal region 11q12-13 shows high meiotic recombination rate around the MEN1 locus[J]. Pree Natl Acad Sci USA, 1991,88(23):10609-10613.
  • 3Agostoni A, Cicardi M. Hereditary and acquired C1-inhibitor deficiency: biological and clinical characteristics in 235 patients[J]. Medicine (Baltimore), 1992,71(4):206-215.
  • 4张宏誉.遗传性血管性水肿[A].见:叶世泰.变态反应学[M].北京:科学出版社,1998.499-505.
  • 5Lung CC, Chan EK, Zuraw BL. Analysis of an exon 1 polymorphism of the B2 bradykinin receptor gene and its transcript in normal subjects and patients with C1 inhibitor deficiency[J]. J Allergy Clin Immunol,1997,99(1 Pt 1):134-146.
  • 6Freiberger T, Vyskocilova M, Kolarova L, et al. Exon 1 polymorphism of the B2BKR gene does not influence the clinical status of patients with hereditary angioedema[J]. Hum Immuno1,2002,63(6):492-494.
  • 7Smith D,Gilbert M, Owen WG, et al. Tissue plasminogen activator release in vlvo in response to vasoactive agents[J]. Blood, 1985,66(4):835-839.
  • 8Hauert J, Nicoloso G, Schleuning WD, et al. Plasminogen activators in dextran sulfate-activated euglobulin fractions: a molecular analysis of factor XII-and prekallikrein-dependent fibrinolysis [J]. Blood, 1989,73(4):994-999.
  • 9Petersen SV, Thiel S, Jensen L, et al. Control of the classical and the MBL pathway of complement activation [J]. Mol Immunol, 2000,37(14):803-911.
  • 10Curd JG, Prograis JLJ, Cochrane CG. Detection of active kallikrein in induced blister fluids of hereditary angioedema patients [J]. J Exp Med, 1980,152(3):742-747.

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