hemophilia

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.

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Conclusions HAART regimen can efficiently inhibit HIV replication of the hemophilia patients who were co-infected with HIV and HCV. HAART can reconstruct the human immune system of the patients with HIV and HCV coinfection.

结论HAART能有效抑制血友病合并丙型肝炎和艾滋病患者体内HIV的复制，有利于免疫功能重建。

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Gene diagnosis of factor ⅷ gene inversion by LD-PCR for 60 patients with severe hemophilia A

应用长距离PCR技术对60例重型血友病甲进行Ⅷ因子基因倒位的基因诊断

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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.

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Hemophilia is caused by a hereditary lack of one of the clotting factors.

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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Adapt the World Hemophilia Day theme to further your own needs.

调整世界血友病日的主题以发展你们自己的需求.

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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。

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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.

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Objective To investigate the feasibility of cadaveric spleen transplantation in the treatment of Hemophilia A.

目的探讨尸体脾移植治疗血友病甲的可行性。

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Hemophilia comes from the Greek haima "blood" and philia "to love."

血友病一词来源于希腊语“haima”，意为“血”，以及“philia”，意为“去爱”。

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Clinical observation of the cadaveric spleen transplantation in the treatment of Hemophilia A

尸体脾脏移植治疗血友病甲的临床观察

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Further Study on Long Distance PCR Detection of Factor ⅷ Inversion Causing Severe Hemophilia A and Its Applications

长距离PCR技术检测重型血友病甲Ⅷ因子基因倒位的进一步研究及推广应用

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Objective To evaluate the effect of spleen transplantation for Hemophilia A and factors involved in spleen function.

目的评价脾移植治疗血友病甲的效果和影响移植脾功能的因素。

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Are Chronic Hepatitis C viral Infections More Benign in Patients With Hemophilia?

丙肝病毒在血友病患者身上表现更温和?

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The safety of intramuscular injection of recombinant adeno-associated virus ( AAV )-mF to rescue hemophilia B was assessed.

研究了肌注腺伴随病毒 ( adeno-associatedvirus,AAV ) 介导凝血因子基因治疗血友病B的安全性.

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Conclusions Living-related-donor spleen transplantation is an effective method to treat hemophilia A.

结论亲属供脾脾脏移植是治疗血友病甲的有效方法，对于控制自发性出血和提高生活质量有重要的意义。

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This is very obvious in genetic diseases, such as familial high blood pressure, daltonism and hemophilia and so on.

这在一些遗传性疾病中就很明显，如家族性高血压、红绿色盲、血友病等。

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Objective To find out the polymorphism distribution of St14 ( DXS52) variable number of tandem repeat ( VNTR) in normal individuals in the northeastern regin of China and hence provide a proof for the gene diagnosis of hemophilia A.

目的探讨中国正常人群St14（DXS52）位点VNTR多态分布，为甲型血友病基因诊断提供依据。

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Progressions of gene therapy studies for hemophilia B were introduced in this paper.

就血友病B的基因治疗研究进展及所存在的问题作一综述.

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Hemophilia treatment Immune tolerance : a nursing perspective.

血友病的治疗.

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Safety assessments required for animal test and preclinical trial of hemophilia B gene therapy

血友病B基因治疗临床试验的安全性研究

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Methods A cadaver spleen transplantation was performed on a 13 year male patient who suffered from hemophilia A. The blood coagulation function, illness recovery, the condition of the transplant spleen and FK506 blood concentration were monitored postoperatively.

方法为1例患血友病甲的男性患儿施行了尸体脾移植手术，术后观察患者凝血功能、病情恢复、移植脾脏状况及免疫抑制剂浓度监测。

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Hemophilia was first described in 1803.

血友病在1803年初次被描述.

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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.

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Long Distance-PCR for Detection of Factor ⅷ Gene Inversion in Patients with Severe Hemophilia A

长距离PCR检测重型血友病A病人凝血因子Ⅷ基因倒位

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Methods Five cases of spleen transplantation performed to treat severe hemophilia A were analyzed retrospectively.

方法回顾性分析5例重症血友病甲行同种异体异位脾移植治疗手术后并发症的诊断及治疗。

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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。

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Study of the Feasibility on That Adipose Tissue-derived Stromal Cells Can Become the Target Cell for Gene Therapy of Hemophilia A

脂肪干细胞作为血友病A基因治疗靶细胞可能性的研究

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The reason it's on April 17 is because that's the birthday of the World Foundation for Hemophilia ( WFH) founder Frank Schnabel.

由于4·17是世界血友病联盟发起人法兰克·舒纳波的生日，所以将该日定为4月17日。

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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.

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