Heterozygosity for the factor V Leiden (G1691A) mutation predisposes renal transplant recipients to thrombotic complications and graft loss. Transplantation 2001; 72:549-50.Wuthrich RP, Cicvara-Muzar S, Booy C, Maly FE. Heterozygosity for the factor V Leiden (G1691A) mutation predispo...
Heterozygosity for the factor V Leiden (G1691A) mutation predisposes renal transplant recipients to thrombotic complications and graft loss. Heterozygosity for a mutation in the coagulation factor V gene (factor V Leiden; FVL) leads to resistance to activated protein C and represents the most co.....
Impact of double heterozygosity for Factor V Leiden and Prothrombin G20210A on the thrombotic phenotype Introduction Because of the rarity of double heterozygosity for Factor V Leiden (FVL) and Prothrombin (FII) G20210A, little is known about the thrombotic p... B Luxembourg,F Henke,A Kirsch-...
Nejat Akar.Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome.European Journal of Pediatrics.2001Sipahi, T., Duru, F., Yarah, N., et al. (2001). Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in ...
He was heterozygous for the G1691A mutation in the Factor V gene, for the G20210A mutation in the prothrombin gene and exhibited decreased activity of the protein S.Conclusions: The genetic predisposition and the severity of his clinical course were seriously considered in order to decide that ...
Sipahi T.Duru F.Yarah N.et a1.Compound heterozygosity for factor V Leiden and prothrombin G20210A nlutalions in a child with Budd --Chiari syndrome.Eru J Pediatr.2001.160(3):198Tansu Sipahi,Feride Duru,Nese Yaralı,Nejat Akar.Compound heterozygosity for factor V Leiden and prothrombin G...
The decision regarding hormone replacement therapy in this lady was complicated due to the presence of Factor V Leiden heterozygosity. A brief discussion and review of the literature follow.KibbeyDepartment of EndocrinologyK.Department of EndocrinologyVincent...
factor V LeidenthrombolysisPaget-Schroetter syndrome or effort thrombosis is characterized by spontaneous thrombosis of the upper extremity venous system, commonly seen in a young healthy patient after repetitive use of the upper extremities. It is rarely associated with coagulopathy and thus, hyper...
Varicella purpura fulminans associated with heterozygosity for Factor V Leiden and transient protein S deficiency. Pediatrics 1998; 102(5): 1208-10. http://dx.doi.org/10.1542/peds.102.5.1208Woods CR, Johnson CA. Varicella purpura fulminans associated with het- erozygosity for factor V leiden and...
Giuseppe Famularo,Giovanni Minisola,Giulio Cesare Nicotra,Claudio De Simone.Mesenteric and portal vein thrombosis associated with hyperhomocysteinemia and heterozygosity for factor V Leiden mutation. World Journal of Gastroenterology . 2005Famularo G, Minisola G, Nicotra GC, Simone CD: Mesenteric and ...