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血友病

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Thus, we call on the government to immediately import Factor VIII to save the lives of haemophiliacs in China.

鉴于上述分析,我们请求我国政府采取紧急行动,从国外大量进口凝血八因子等血制品,抢救我国血友病人的生命。

The plaintiffs alleged that the companies manufactured and sold blood factor products as beneficial "medicines" that were, in fact, contaminated with HIV and/or HCV and resulted in the mass infection and/or deaths of thousands of haemophiliacs worldwide.

这些原告声称,这些公司生产并售出&有益的血液因子产品药物&,但是,实质上,这些药物被感染了HIV和HCV,并导致大量的感染和世界范围内数以千计的血友病患者的死亡。

The Lindsay Tribunal was set up in Ireland in 1999 to investigate the infection of haemophiliacs with HIV and Hepatitis C from contaminated blood products supplied by the Blood Transfusion Service Board.

1999年,林夕法庭在爱尔兰成立,目的是调查输血服务委员会供应的受污染的血液制品所引起得血友病患者感染HIV和丙型肝炎事件。

The Chinese government should abolish the ban of imports of clotting factors, and should immediately import a large volume of clotting factor products. This will give Chinese haemophiliacs more options, and complement the shortage of domestic clotting factor production. In 1986, the Ministry of Health issued a circular to prohibit the import of Factor VIII and similar blood products to prevent the inflow of HIV/AIDS and other diseases.

我国政府应解除禁止进口国外凝血因子的政策,尽快引进国外的凝血因子制品,为血友病患者提供更多的选择余地,以弥补国内凝血因子产品供不应求的情况。1986年1月30日,卫生部发布《关于禁止进口Ⅷ因子等血液制品的通告》目的是阻止进口血液制品将艾滋病等传染病带入中国。

This is true despite the multiple blood supply scandals of the past decade: from the large number of plasma sellers who contracted HIV via inappropriate collection procedures in the mid-1990s; to the many haemophiliacs in and outside Shanghai who find themselves carrying HIV and hepatitis since the new millennium, to people infected with HIV/AIDS via blood transfusions and blood products.

自从20世纪90年代中期出现的中原血祸(大量卖血浆者感染艾滋病病毒)、到进入21世纪以来发现的大量上海和上海以外地区的血友病人发现感染艾滋病病毒和肝炎病毒、到遍布全国的输血感染艾滋病病毒者,我们却震惊地发现,我国政府一直缺乏一个综合处理相关血液及制品供应和安全事务的协调机制。

As antithrombin III, an anti-clotting protein for heart patients, or Factor IX, a clotting protein for haemophiliacs.

如为心脏病患者提供一种抗血栓蛋白质——抗血栓III,或者为血友病患者提供一种凝血蛋白质——凝血因子IX。

As antithrombin III, an anti- clot ting protein for heart patients, or Factor IX, a clot ting protein for haemophiliacs.

如为心脏病患者提供一种抗血栓蛋白质——抗血栓III,或者为血友病患者提供一种凝血蛋白质——凝血因子IX。

Von willebrand factor is one glycosylated protein synthesized by blood vessel endothelial cell.Thrombomodulin is one glucoprotein which exists in blood vessel endothelial cell surface.Both of their levels are increased obviously when endotheliocyte is damaged,so they could be considered as the molecular markers reflecting endothelial injury.

血管性假血友病因子是血管内皮细胞合成的一种糖基化蛋白,血栓调节蛋白是位于血管内皮细胞表面的糖蛋白,内皮细胞损伤时,二者水平均显著升高,因此它们作为反映内皮损伤的分子标记物。

Methods:In patients with ACS(n=32) and controls(n=21) the selective coronary arteriography was performed and the coronary artery stenosis scores were evaluated through accumulative total integration. Plasma concentrations of fibrinogenwere determined with hemagglutinin analysator and plasma concentrations of von Willebrand factor、 D-Dimer、 plasminogen activator inhibitor、platelet membrane glucoprotein(GMP-140) were determined with enzyme linked immunosorbent assay.

选择ACS患者32例和对照组21例进行选择性冠状动脉造影,对冠脉造影结果采用累计积分法进行冠状动脉狭窄评分;使用血凝分析仪测定受试者血浆纤维蛋白原水平,使用酶联免疫法测定外周静脉血血管性血友病因子、D-二聚体、纤溶酶原激活剂抑制物、血小板膜糖蛋白140(GMP-140)的含量。

Hemophilia is caused by a hereditary lack of one of the clotting fac to rs.

血友病就是因为遗传上缺乏一种凝血胶原引起的。

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