Hemophilia was first described in 1803.
血友病在1803年初次被描述。
If you have hemophilia do not get tattoo.
假如你有血友病不要纹身。
Hemophilia a was first described in 1803.
血友病在1803年初次被描述。
Celebrate 20 years of World Hemophilia Day.
庆祝世界血友病日20年。
How does hemophilia affect the lives of those involved?
血友病是如何影响患者生活的？
Support your hemophilia treatment centre and comprehensive care team.
支持你们的血友病治疗中心和综合治疗团队。
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。
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。
These disorders may include cystic fibrosis, hemophilia, sickle cell anemia, and many others.
这些变异包括包囊纤维症、血友病、镰状细胞贫血症和其他多种疾病。
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。
After being diagnosed with hemophilia, he had to be careful not to get cut or he could bleed to death.
在被确诊为血友病之后，他必须小心翼翼地避免被割伤，否则他会流血不止而死亡。
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。
Lack of factor VIII causes classic hemophilia; other types are caused by deficiency of factor IX or XI.
在典型的血友病中缺乏的是凝血因子VIII；其它的血友病是因缺乏凝血因子IX或XI。
Musculoskeletal manifestations of hemophilia include hemophilic arthropathy and hemophilic pseudotumor.
血友病的骨肌表现包括血友病性关节病和血友病性假肿瘤。
Hemophilia can be mild, moderate, or severe, depending on how much clotting factor is present in one's blood.
血友病可以是轻微、温和的，或者是剧烈的，这是根据人体血液里凝血因子的多少而定。
As genetic blood disorders, hemophilia and porphyria had serious effects on the crowned heads of Europe.
血友病和卟啉病这两种遗传性血液病，在欧洲的皇室内产生了严重的影响。
The National Hemophilia Information Management Center says there are nearly 8, 000 registered cases in China.
国家血友病信息管理中心说中国有接近8000例登记在案。
CONCLUSION: HCV infections in hemophiliacs may be less severe than in HCV infected patients without hemophilia.
结论：在血友病患者中的HCV感染相对于无血友病患者中的HCV感染程度较轻。
This article gives the important information about hemophilia, hemophilia symptoms and treatment for the hemophilia.
本文给出了有关的重要信息血友病，血友病的症状与治疗血友病。
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。
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。
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。
The aim of this study was to investigate the efficacy of hepatocyte transplantation in the mouse model of hemophilia B.
该研究的目的在于研究肝细胞移植在小鼠B型血友病模型中的效果。
Researchers have long dreamed of treating diseases from hemophilia to cancer by replacing mutant genes with normal ones.
研究人员长期以来一直梦想用正常基因取代突变基因的方法治疗血友病，癌症等各种疾病。
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。
Objective To improve the physician' s understand of acquired hemophilia (AH) , and discuss optimal therapy schemes of AH.
目的提高对获得性血友病（AH）的认识，探讨其最佳治疗方案。
Because our country also once reported the hemophilia patient to use imports the elder sister factor to infect HIV the instance.
我国也曾报道过血友病病人因使用进口第姐因子而感染HIV的事例。
Because our country also once reported the hemophilia patient to use imports the elder sister factor to infect HIV the instance.
我国也曾报道过血友病病人因使用进口第姐因子而感染HIV的事例。
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