Hemophilia a was first described in 1803.
血友病在1803年初次被描述。
Objective:To improve the gene diagnosis and carrier detection in for hemophilia A patients and their family members.
目的：探讨提高血友病A患者及家系成员的基因诊断、携带者检出的诊断率的途径。
Objective To find out a simple and specific method for genetic diagnosis of hemophilia a and identification of carriers.
目的探索一种更简便和更特异的方法，用于血友病a的基因诊断及其家系遗传咨询。
Our results suggested that if problem of rejection could be resolved, the fetal splenic transplantation would be an effective treatment for hemophilia A.
研究结果提示术后近期均显一定效果．若能解决排斥等问题，此法可望成为治疗血友病甲的有效方法。
Objective:To improve the skills of diagnosing severe hemophilia A(HA)and the carriers of the disease by detection of coagulation factor VIII(FVIII)gene inversion.
目的：检测凝血因子VIII基因倒位，提高对重型血友病A患者及其携带者的诊断水平。
A division of deerfield illinois-based Baxter healthcare corp based in glendale California is another biotech pioneer. it introduced the first biotech drug for hemophilia a in1992.
位于伊利诺斯州鹿园的贝克斯特康复公司在加州的格林·代尔设有分部。这个分公司是生物技术方面的又一个先锋，于1992年推出第一种治疗a型血友病的生物技术药。
The family apparently suffered from a very rare form of hemophilia, indeed.
这一家族似乎真的罹患一种罕见的血友病。
Queen Victoria and many of her descendants carried what was once called "Royal disease" -now known as hemophilia, a blood clotting disorder.
维多利亚女皇和她许多子孙后代携带有一度被称为“皇室病”的疾病——即现在的血友病，一种血液凝结的混乱症。
Hemophilia is a rare blood disorder, and people born with this condition have little or no clotting factor, a protein that controls bleeding.
血友病是一种罕见的血液疾病，遗传这种病的人极少或没有凝血因子，这些正是一种控制出血的蛋白质。
Hemophilia is caused by a mutation—likely spontaneous in Victoria‘s case—on the X chromosome and can be passed along the maternal line of families.
血友病源于X染色体上的一种突变——很可能是维多利亚女皇自身发生的一种突变，可经由遗传系统传给家族后代。
In human trials of the hemophilia treatment, patients show a response at first, but it fades over time.
在治疗血友病的人体试验中，病人最初有一些反应，但经过一段时间，这种反应就消失了。
In January, a hemophilia sufferer revealed online that Baidu had sold moderation rights for several disease-related forums, and as a result, users received dubious medical advise.
今年一月，一位血友病患者在网上揭露百度将血友病吧经营权卖给他人，导致许多用户接收到可疑的医疗建议。
Fibrin and platelets combine to form a clot. Hemophilia is caused by a hereditary lack of one of the clotting factors.
血纤维蛋白和血小板一起形成血栓。血友病就是因为遗传上缺乏一种凝血胶原引起的。
We will learn how to manufacture Factor 8, a rare and expensive medicine used to treat hemophilia.
我们将能在轨道上试验制作“第八因子”，这是一种非常珍贵的稀有药物，可以治疗血友病。
A 29 year old woman with a family history of hemophilia B asked for prenatal diagnosis in the 8th week of pregnancy.
一例有血友病B家族史的29岁孕妇，于妊娠8周时要求对胎儿进行诊断。
Hemophilia: Hereditary Bleeding disorder caused by deficiency of a coagulation factor.
血友病：一种遗传性出血性疾病，因先天性缺乏某种凝血因子而引起。
Method:Analyzed of 5 a hemophilia concomitant with bone and joint injuries which were admitted from 1980, Jan. to 2003, Jan. The mean follow-up the was 11months.
方法：回顾分析我院1980 1～ 2 0 0 3 1收治的5例合并骨关节损伤的甲型血友病患者的术前及术中、术后的治疗，并随访平均11个月。
Method:Analyzed of 5 a hemophilia concomitant with bone and joint injuries which were admitted from 1980, Jan. to 2003, Jan. The mean follow-up the was 11months.
方法：回顾分析我院1980 1～ 2 0 0 3 1收治的5例合并骨关节损伤的甲型血友病患者的术前及术中、术后的治疗，并随访平均11个月。
应用推荐