Heterozygosity for the factor V Leiden (G1691A) mutation predisposes renal transplant recipients to thrombotic complications and graft loss. Transplantation. 2001;72:549-550.Wuthrich RP,Cicvara Muzar S,Booy C. Heterozygosity for the factor V Leiden (G1691A) mutation predisposes renal tra...
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-...
Factor II and factor V (Leiden) heterozygosity in a case of deep vein thrombosis and pulmonary embolismBackground: Venous thromboembolism is a multifactorial disease that depends on a variety of acquired and genetic risk factors. Pulmonary embolism is usually considered to be a complication of deep...
Compound heterozygosity for factor VLeiden and prothrombin G20210A mutations in a child with Budd- Chiarisyndrome [ J ]. Eur J Pediatr ,2001,160 ( 3 ) : 198.Tansu Sipahi Feride Duru Nese Yaral? Nejat Akar.Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a ...
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 C deficiency. Pediatrics 1998;102:1208-10.Woods CR, Johnson CA. Varicella purpura fulminans associated with heterozygosity for factor V Leiden and transient protein S deficiency. Pediatrics. 1998;102:1208...
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 ...