People with hemophilia A, the most common form of the disease, are deficient in Factor VIII and suffer episodes of uncontrolled bleeding. A型血友病是血友病中最常见的类型。病人第8因子缺失,罹患无法控制的出血。
F ⅷ Gene Mutation Spectrum in Chinese Hemophilia A Patients 中国血友病A患者基因突变谱的研究
Clinical Analysis and Laboratory Findings in A Patient with Acquired Hemophilia A 获得性血友病A的临床分析与实验室检查
Frequency of Factor ⅷ Inhibitor in the Patients with Hemophilia A and Environmental Risk factors for Inhibitor Development 血友病A患者因子Ⅷ抑制物的检出率及抑制物产生的环境因素
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 gene diagnosis, carrier detecting and prenatal diagnosis for hemophilia A families to a maximum. 目的最大限度地提高血友病A(HA)患者及家系成员的基因诊断、携带者检出及产前诊断的可诊断率。
Objective To investigate the feasibility of prenatal diagnosis in hemophilia A by fetal umbilical blood. 目的探讨应用脐带血对血友病A进行产前诊断的可行性。
Study on Developing New Technology of Diagnosis for Severe Hemophilia A and Its Application 重型血友病甲基因诊断新技术的研究及其应用
A male fetus was suspected of having hemophilia A. 1例为怀疑患血友病A的男胎;
The Prenatal Diagnosis of Hemophilia A& The Use of PCR and Family RFLP Analysis 甲型血友病产前诊断&应用DNA聚合酶链反应(PCR)进行家系RFLP连锁分析
Objective To develop a rapid and efficient single cell PCR method for hemophilia A non-invasive prenatal genetic diagnosis. 目的建立快速有效进行血友病A基因诊断和性别鉴定的单细胞PCR策略和方法。
Study of Prenatal Diagnosis in Hemophilia A by Fetal Umbilical Blood 应用脐血对血友病A进行产前诊断的研究
Application of long distance-PCR to hemophilia A carrier detection and prenatal diagnosis 长距离PCR在血友病A携带者检测和产前诊断中的应用
Objective: To identify the genetic defect of a patient with severe hemophilia A ( SH9). 目的:检测一例重型血友病A患者(SH9)的基因突变。
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。
Development of modern biotechnology and treatment of hemophilia A 现代生物技术的发展与血友病甲的治疗
Progress on DNA diagnosis of hemophilia A by microsatellite 微卫星及在血友病甲基因诊断中的研究进展
Clinical and cost implications of target joints in Canadian boys with severe hemophilia A 加拿大重度A型血友病患儿的临床和费用问题的研究
Carrier detection and prenatal diagnosis for hemophilia A 血友病A携带者检测与产前诊断
Preliminary experimental research on gene therapy for hemophilia A 血友病A基因治疗的初步实验研究
Recombinant Factor ⅷ for Treatment of Patients with Hemophilia A in China 基因重组人凝血因子Ⅷ在中国人血友病A患者中使用的研究
Study on intron 22 inversion with the patients of hemophilia A 血友病A内含子22倒位的初步研究
Polymorphisms of the factor ⅷ gene in Chinese and prenatal diagnosis of hemophilia A 中国人凝血因子Ⅷ基因多态性和血友病A的产前诊断
Study on Gene Diagnosis in Hemophilia A by Microsatellite DNA Polymorphism 用微卫星DNA多态性进行血友病甲基因诊断的研究
DNA Diagnosis of A Family with Hemophilia A through RFLPs 用RFLPs对一个血友病A家系进行基因诊断
Objective To understand the infection with hepatitis B virus ( HBV), Human immunodeficiency virus ( HIV) and syphilis in patients with hemophilia A. 目的了解血友病甲患者乙型肝炎病毒(HBV)、艾滋病病毒(HIV)及梅毒的感染情况。
Gene Diagnosis of Hemophilia A by PCR PCR技术在甲型血友病基因诊断中的应用
On the other hand, it has been observed that venous thrombosis is very rare in hemophilia A patients. 另一方面,对血友病A的患者观察发现发生静脉血栓的情况很少。