... Hereditary factor VIII deficiency 遗传性因子Ⅷ缺乏 hereditary factor XIII deficiency 缺乏症 ... dict.youdao.com|基于1 个网页 2. 缺乏 什么意思... ... Hereditary factor VIII deficiency 遗传性因子Ⅷ缺乏 hereditary factor XIII deficiency 缺乏症 ... dict.youdao.com|基于1 个网页...
The bleeding patterns were those of mild to moderate haemophilia B and did not appear to have been modified by the presence of factor-VII deficiency.C.HematologyA.HematologyHallHematologyA.HematologyR.HematologyLondonHematologyA.HematologyC.Hematology...
(1993), Combined hereditary factor XI (plasma thromboplastin antecedent) deficiency, von Willebrand's disease, and xeroderma pigmentosum in a Japanese family. Am. J. Hematol., 44: 129–133. doi: 10.1002/ajh.2830440211 Author Information 1 Division of Hematology, Department of Internal Medicine, ...
Conclusions A novel compound heterozygous mutation of GIF in a Chinese patient of hereditary intrinsic factor deficiency was reported. It was the first identified mutation of GIF in East-Asia and may indicate a new ancestry. 展开 关键词: Megaloblastic anemia Cobalamin deficiency Intrinsic factor ...
Von Willebrand Disease (VWD) is a bleeding disorder caused by a deficiency of a protein called von Willebrand Factor. Learn More About VWD Hemophilia A Hemophilia A is a bleeding disorder caused by a deficiency in blood clotting Factor VIII. ...
Von Willebrand Disease (VWD) is a bleeding disorder caused by a deficiency of a protein called von Willebrand Factor. Learn More About VWD Hemophilia A Hemophilia A is a bleeding disorder caused by a deficiency in blood clotting Factor VIII. ...
Von Willebrand Disease (VWD) is a bleeding disorder caused by a deficiency of a protein called von Willebrand Factor. Learn More About VWD Hemophilia A Hemophilia A is a bleeding disorder caused by a deficiency in blood clotting Factor VIII. ...
Hereditary Protein S Deficiency 喜欢 0 阅读量: 18 作者:M R.,Bertina 摘要: Protein S is a vitamin K-dependent plasma protein that serves as a cofactor of activated protein C (APC) in its inhibitory action on activated factor V and factor VIII and in its stimulation of fibrinolytic activity...
The second child (IX 3) died of SCIO in 1973, but before his death complete deficiency of ADA could be ascertained (32). The father (VIII 3) and one of his brothers (VIII 4) have significantly diminished ADA activity, but the mother's (VIII 6) and two of her sisters' (VIII 7 ...
Hereditary defect in biosynthesis of aldosterone: aldosterone synthase deficiency 1964-1997. We studied two of the three patients with a hereditary defect in the biosynthesis of aldosterone originally described by Visser and Cost in 1964. All three... M Peter,L Fawaz,SL Drop,... - 《Journal of...