Diagnosis of Radiography Image of Arthropathies in Patients with Hemophilia;
血友病骨关节病变的X线诊断
Testing study on Chinese version of "Canadian hemophilia outcomes-kids' life assessment tool";
“加拿大血友病儿童生活质量评估工具”中文版测试研究
A review of holistic care model for patients with hemophilia in China and western countries;
我国及欧美血友病综合关怀模式的现状
Perioperative management of children suffering from haemophilia;
手术患儿合并血友病的围手术期处理
Observations of Four Haemophilia Patients Infected with HIV;
4例血友病HIV感染者的追踪观察
TSAH(Traumatic Subarachnoid Haemorrhage),is not seldom seen in forensic pathological practice and clinical medicolegal expertise however,relevant reports about the phenomena that haemophiliacs suffer from simple TSAH when their heads or faces are slightly hurt are relatively rare.
外伤性蛛网膜下腔出血(Traumatic Subarachnoid Haemorrhage,简称TSAH)在法医病理实践和临床法医鉴定中并不少见,但有关血友病人在头面部轻微外伤后出现单纯性TSAH的相关报道较少,在临床法医鉴定中有一起损伤和疾病同时存在的特殊案例,在该案例鉴定中有一些体会值得借鉴。
Prenatal diagnosis in eleven families with hemophilia A of inversion negative in intron 22 of factor Ⅷ gene;
非凝血因子Ⅷ基因内含子22倒位型血友病A家系11例产前诊断
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
Analysis and Detected the Intron Repeat Sequence of Facor Ⅷ Gene Polymorphism with Hemophilia A and Their Family Members;
血友病A家系因子Ⅷ基因内含子重复序列多态性的检测及分析
Haemophilia b is a kind of serious cruor-defective inhering diseaes.
血友病B是一种严重的凝血功能缺陷遗传病 ,由于现行的治疗方法对血友病B的治疗效果均不令人满意。
In order to establish coagulation factor Ⅸ gene knockout mouse for human haemophilia B, 2×105 phage plaques of 129Sv mouse genomic library were screened with plaque in situ hybridization screening with 32P-labeled cDNA probe 5 positive clones were finally obtained.
为了利用ES细胞基因打靶技术建立人血友病B的转基因小鼠模型，用小鼠FIX基因cDNA为探针，筛选129Sv小鼠的基因组DNA噬菌体文库，从2×105个噬斑中得到5个独立的阳性噬菌体克隆。
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 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
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
Of, relating to, or affected by hemophilia.
血友病的血友病的，与血友病有关的，患血友病的
A person who is affected with hemophilia.
血友病患者感染血友病的人
Globulin Antihemophilia
抗血友病球蛋白[因子Ⅷ]
A haemophiliac's blood will not clot properly.
血友病患者的血液凝固不良.
Changes of vWF in Patients with Polycystic Ovary Syndrome
PCOS患者血管性假血友病因子水平变化
someone who has hemophilia and is subject to uncontrollable bleeding.
患有血友病并且遭受无法控制的流血疾病的人。
Surgical treatment for hemophilic pseudotumors and arthritis of limbs
四肢血友病假瘤及血友病关节炎的外科治疗意义
THE RELATIONSHIP BETWEEN ESSENTIAL HYPERTENSION AND PLASMA LEVELS OF vWF AND ACTIVITY OF vWF-cp
高血压病患者血浆血管性血友病因子及其裂解酶的变化
Hemophilia was first described in 1803.
血友病在1803年初次被描述。
anti-hemophilic globulin deficiency
抗血友病性球蛋白缺乏症
FⅧ Gene Mutation Spectrum in Chinese Hemophilia A Patients
中国血友病A患者基因突变谱的研究
The bio-therapy and gene-therapy of hemophilia B in China
中国血友病B生物基因治疗研究状况
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。
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。
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。
The Mark of Endothelial Cell Dysfuction-E-selectin and vWF in Hypertensive Disorder Complicating Pregnancy(HDCP);
E-选择素、血管性假性血友病因子与妊娠期高血压疾病
Clinic Research of Von Willebrand Factor and D-dimer in Hypoxic Ischemic Encephalopathy;
血管性血友病因子、D-二聚体与新生儿缺氧缺血脑病的临床研究
Treatment of mild hemophilia resulted in bleeding after tonsillectomy
轻症血友病患者扁桃体切除术后出血的处理