Introduction: Factor XI is a glycoprotein that important role in blood coagulation. The aim of thisstudy is determine correlation of thrombotic factor and bleeding severity with factor XI deficiency.Materials and Methods: 24 patients with factor XI deficiency were included in this study. Followingphysical examination and interview, a questionnaire was filled for all the patients. A blood sample wascollected for measurement of coagulation factors (II, V, VII, and VIII, IX, X, XI, XII, and XIII),fibrinogen, protein C, protein S, antithrombin III, PG20210A, factor V Leiden, MTHFR gene andHomocystein.Results: 54.2% and 45.8% of patients were male and female, respectively. Mean (±SD) age of patientswas 27.2±13.6 (3-49) years. 45.8%, 29.2%, 25% o...
Factor XI (FXI) is a serine protease involved in the propagation phase of coagulation and in providi...
Introduction: Hemophilia is the most common disorder of deficiencies in thrombotic factors. Inmost p...
bleeding disorder, is rare worldwide but common in Jews in whom 2 mutations, Glu117Stop (type II) an...
Background: Factor XI, a component of the intrinsic pathway of coagulation, contributes to the gener...
International audienceBleeding risk is not predictable in patients with factor XI (FXI; F11) deficie...
Currently available evidence supports the contention that elevated levels of factor XI (fXI) are ass...
Introduction: Factor XI deficiency or hemophilia C is a very rare coagulation factor deficiency, wit...
Background and Objectives. In patients with factor XI (FXI) deficiency the bleeding tendency is poor...
We describe a patient with a prolonged aPTT who was diagnosedas having factor XI deficiency after a ...
Factor XI (FXI) deficiency is a rare autosomal recessive disorder. Many patients with even very low ...
In factor XI (FXI) deficiency, bleeding cannot be predicted by routine analyses. Since FXI is involv...
Blood coagulation is a complex system in which the proteins of the coagulation cascade play an impor...
The management of factor XI deficiency is not straightforward for three reasons: firstly, the role o...
Background In factor XI (FXI) deficiency, bleeding cannot be predicted by routine analyses. Since FX...
Factor XI deficiency is a rare autosomally transmitted coagulopathy that is associated with a variab...
Factor XI (FXI) is a serine protease involved in the propagation phase of coagulation and in providi...
Introduction: Hemophilia is the most common disorder of deficiencies in thrombotic factors. Inmost p...
bleeding disorder, is rare worldwide but common in Jews in whom 2 mutations, Glu117Stop (type II) an...
Background: Factor XI, a component of the intrinsic pathway of coagulation, contributes to the gener...
International audienceBleeding risk is not predictable in patients with factor XI (FXI; F11) deficie...
Currently available evidence supports the contention that elevated levels of factor XI (fXI) are ass...
Introduction: Factor XI deficiency or hemophilia C is a very rare coagulation factor deficiency, wit...
Background and Objectives. In patients with factor XI (FXI) deficiency the bleeding tendency is poor...
We describe a patient with a prolonged aPTT who was diagnosedas having factor XI deficiency after a ...
Factor XI (FXI) deficiency is a rare autosomal recessive disorder. Many patients with even very low ...
In factor XI (FXI) deficiency, bleeding cannot be predicted by routine analyses. Since FXI is involv...
Blood coagulation is a complex system in which the proteins of the coagulation cascade play an impor...
The management of factor XI deficiency is not straightforward for three reasons: firstly, the role o...
Background In factor XI (FXI) deficiency, bleeding cannot be predicted by routine analyses. Since FX...
Factor XI deficiency is a rare autosomally transmitted coagulopathy that is associated with a variab...
Factor XI (FXI) is a serine protease involved in the propagation phase of coagulation and in providi...
Introduction: Hemophilia is the most common disorder of deficiencies in thrombotic factors. Inmost p...
bleeding disorder, is rare worldwide but common in Jews in whom 2 mutations, Glu117Stop (type II) an...