血友病患者的血液中缺乏凝血因子 VIII。
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 a rare blood disorder, and people born with this condition have little or no clotting factor, a protein that controls bleeding.
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。
Hemophilia can be mild, moderate, or severe, depending on how much clotting factor is present in one's blood.
地中海贫血和镰状细胞病等病症患者还需要定期输血，并且血液被用于制造各种制品，例如供血友病患者使用的凝血因子。
It is also needed for regular transfusions for people with conditions such as thalassaemia and sickle cell disease and is used to make products such as clotting factors for people with haemophilia.
这些观察结果显示发生的不良反应必须用凝血因子解释，而不是用高分子重量和多个高分子的聚集。
The observations suggested that the reactions which occurred must be explained by factors other than high molecular weights or aggregates of molecules.
这可以进展为慢性肝病和肝硬化，肝脏中瘢痕组织如此广泛以至于无法净化血液或生产重要激素及凝血因子。
This can progress to chronic liver disease and cirrhosis where the scarring is so extensive the liver is unable to clean blood or produce vital hormones and clotting factors.
微栓塞能够引起组织缺血，红细胞片断引发溶血性贫血，或者血小板和凝血因子消耗导致出血。
Microscopic thrombi can produce tissue ischemia, red cell fragmentation leading to a hemolytic anemia, or hemorrhage due to consumption of platelets and clotting factors.
目的研究缺氧缺血新生猪凝血状态，以及部分凝血因子促凝活性的动态变化，探讨缺氧缺血性脑损伤（HIBD）时凝血功能变化。
Objective To investigate the changes of blood coagulation state and some prothrombin's function in newborn piglets at different time after hypoxic-ischemic brain damage (HIBD).
肝脏产生的抗凝血因子升高，因而内皮组织产生的VIII因子和血管假性血友病因子也升高。
These anti-coagulants are made in the liver and consequently Factor VIII and Von Willebrand factor will go up which are made in the endothelium.
目的：探讨原发性系统性淀粉样变性并发凝血因子x缺乏的临床特征、发病机制及治疗方法。
Objective: to investigate the clinical feature, pathogenesis, and therapy of Primary systemic amyloidosis with acquired factor-X deficiency.
目的探讨凝血因子和纤溶指标在病毒性肝炎和妊娠肝炎中的变化和意义。
Objective to explore the clinical significance of coagulation factor and fibrinolytic indexes in viral hepatitis and pregnant hepatitis.
肝制造血浆蛋白质，包括白蛋白和凝血因子，并合成以改变营养物和毒素等物质，并把它们从血液中滤出。
The liver manufactures plasma proteins, including albumin and clotting factors, and synthesizes enzymes that modify substances such as nutrients and toxins, filtered from the Blood.
结论：蝎毒对家兔凝血功能的影响除通过降低血液粘度外，还可能是蝎毒影响了凝血因子的功能所致。
Conclusion: the mechanism of Scorpion Venom restraining the blood coagulation probably function are that Scorpion Venom reduce blood viscosity and affects the function of blood coagulation factors.
凝血因子能够从血浆中分离，用于治疗凝血因子缺乏的患者，如血友病。
Coagulation factors can be removed from plasma and may be used to treat people with coagulation factor deficiencies, such as hemophilia.
目的探讨凝血因子VII (FVII)活性与其多态性的关系。
Objective to investigate the relationship between coagulation factor VII (FVII) activity and polymorphism.
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。
Lack of factor VIII causes classic hemophilia; other types are caused by deficiency of factor IX or XI.
妊娠肝炎组的凝血因子水平高于正常对照组，但低于正常晚孕组。
Plasma levels of coagulating factors in pregnant hepatitis were higher than those in control, but lower than those in normal pregnancy.
结论：凝血因子XII缺乏症是与习惯性流产有关联。其他因素数据，不能表明和习惯性流产的关系，或者这种关联是受限制的。
CONCLUSION: factor XII deficiency is associated with recurrent miscarriage. Data on the other factors either fail to show association or are quite limited.
凝血因子VIII主要给血友病患者提供其所缺少的血液凝结的成分。
Factor VIII essentially provides the missing ingredient without which hemophiliacs' blood cannot clot.
新鲜冷冻血浆及冷沉淀物(常简称为冷沉淀)可输给凝血因子异常或缺乏的患者(比如，血友病患者)。
Fresh frozen plasma (FFP) and cryoprecipitate, often called "cryo" for short, are transfused to patients who have abnormal or low levels of blood clotting proteins, such as in hemophilia.
这一过程是由一系列酶和辅因子催化的，这些酶和相关的辅因子统称为凝血因子。
This process catalysis by a series of enzymes and cofactors. These enzymes and cofactors all be called coagulation factor.
目的探讨高脂血症血脂和凝血因子的变化与中医辨证分型的关系。
Objective to explore the relation between the changes of blood lipid and blood coagulation factors in hyperlipidemia with Traditional Chinese Medicine (TCM) type.
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。
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.
目的探讨妊娠期高血压疾病妇女血浆凝血因子的变化及临床意义。
Objective To explore the changes of plasma levels of PT, APTT, fibrinogen in pregnancy complicating with hypertension and its clinical significance.
剩下的10%是营养物质，电解质(溶解盐)、气体、白蛋白(一种蛋白质)，凝血因子，抗体、废弃物、酶、激素。
The remaining 10% contains nutrients, electrolytes (dissolved salts), gases, albumin (a protein), clotting factors, antibodies, wastes, enzymes, and hormones.
凝血因子XIII缺乏症患者顾名思义，就是不能生成足够的凝血因子XIII，而凝血因子XIII在血液中循环，是参与正常的凝血的重要一个成分。
Patients with congenital Factor XIII deficiency don't make enough Factor XIII, a substance that circulates in the blood and is important for normal clotting.
目的：观察急性单核白血病（AML-M5）止凝血因子标志物的变化，探索AML-M5患者出血机制及这些标志物在疾病诊疗、预后判断中的意义。
Objective:To study the changes of hemostatic molecular markers inacute monoblastic leukemia (AML-M5) for elucidate the mechanism of hemorrhage and its clinical significance.
研究发现，出血及血栓等多种疾病与人体中凝血因子的含量多少有着密切的联系。
The results show that bleeding and thrombosis is closely related to content of coagulation factor in human's blood.
凝血障碍，定义是实验室检查有血管内凝血因子消耗或溶纤或严重的出血，且无法找到其他可能的原因来解释。
Coagulopathy, defined as laboratory evidence of intravascular consumption or fibrinolysis or severe clinical hemorrhage in the absence of other explanations.
凝血障碍，定义是实验室检查有血管内凝血因子消耗或溶纤或严重的出血，且无法找到其他可能的原因来解释。
Coagulopathy, defined as laboratory evidence of intravascular consumption or fibrinolysis or severe clinical hemorrhage in the absence of other explanations.
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