Girolami A,Simioni P,Scarano L,et al.Sym ptomatic combined homozygous factor Ⅻ deficiency and heterozygous factor V Leiden[J].J Thromb Thrombolysis;2000,9(3):271-275.Girolami A,Simioni,P Scarano L,et al.Symptomatic combined homozygous factor Ⅻ deficiency and heterozygous factor V Leiden[J...
Resistance to activated protein C (APC) is a common inherited risk factor for venous thrombosis, which is associated with a mutation in coagulation factor V (factor V Leiden). We investigated the risk of venous thrombosis in individuals homozygous for this abnormality. We determined the factor V...
factor V LeidenBudd-Chiari syndromeComment on Br J Haematol. 1998 Sep;102(4):929-31.doi:10.1046/j.1365-2141.1999.01487.xGurjeewan GarewalReena DasYogesh ChawlaR K DhimanBlackwell Science LtdBritish Journal of HaematologyGarewal G,,Das R,Chawla Y.Budd-Chiari syndrome associated with homozygous ...
Prevalence of the factor V Leiden mutation in hepatic and portal vein thrombosis. The factor V Leiden (FVL) mutation has been shown to be the most frequent cause of hereditary thrombophilia. The prevalence of the mutation in patients wit... AE Mahmoud,E Elias,N Beauchamp,... - Gut 被引量...
Standen GR, Morse C et al.DVT following oral contraceptive therapy in association with homozygous factor V Leiden. Aslam S. Clinical and Laboratory Haematology . 1995Aslam S.Standen GR, Morse C et al.DVT following oral contraceptive therapy in association with homozygous factor V Leiden.Clinical ...
Homozygous APC-resistance combined with inherited type I protein S deficiency in a young boy with severe thrombotic disease. Inherited resistance to activated protein C (APC) is a frequent cause of familial thrombosis. It is associated with a factor V gene point mutation replacin... Bengt Zller...
High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance) Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver dise...
Kyung A. Kang
Idiopathic Deep Vein Thrombosis in Siblings with Homozygous Factor V Leiden Mutation 来自 Semantic Scholar 喜欢 0 阅读量: 21 作者:H Köppel,W Renner,G Seinost,E Pilger 摘要: Kppel H, Renner W, Seinost G, Pilger E.关键词:thrombus formation von Willebrand factor collagen HMEC-1 shear rate...
The early and severe clinical manifestations in the homozygous proband may be explained by the severity of the AT deficiency; however, a role of the additional genetic risk factor, heterozygosity for factor V Leiden, cannot be ruled out. Fewer than 20 cases of homozygous AT deficiency have so ...