The spectrum of bleeding problems in FVII deficiency is highly variable and FVII levels and causative genetic mutations correlate poorly with the bleeding risk. Long-term prophylaxis is generally initiated in order to prevent subsequent CNS bleeding after a first event or in patients with other major/ life threatening/ frequent bleeding symptoms as gastrointestinal bleeding or hemarthrosis. However few data are available in the literature regarding FVII prophylaxis and clinical decisions cannot be based on evidence
We performed a prospective study of FVII inhibitor occurrence in a large number of patients with FV...
Activated factor VII (FVIIa), the first protease of clotting, expresses its physiological procoagula...
Factor VII deficiency is a rare bleeding disorder showing an autosomal recessive pattern of inherita...
Inherited factor VII (FVII) deficiency is a rare autosomal recessive disorder associated with a blee...
Patients with inherited factor VII (FVII) deficiency display different clinical phenotypes requiring...
Background: Inherited factor VII (FVII) deficiency is the most common among rare congenital bleeding...
The complex formed between the procoagulant serine protease activated factor VII (FVII) and the memb...
The complex formed between the procoagulant serine protease activated factor VII (FVII) and the memb...
Individuals with inherited factor VII (FVII) deficiency display bleeding phenotypes ranging from mil...
Aim: Factor VII deficiency is one of the hereditary coagulation disorders that has autosomal reccess...
BackgroundIn congenital Factor (F) VII deficiency bleeding phenotype and intrinsic FVII activity lev...
Factor VII deficiency is the most common among rare inherited autosomal recessive bleeding disorders...
Analysis of biological phenotypes from 42 patients with inherited factor VII deficiency: can biologi...
: Congenital factor VII (FVII) deficiency is a rare bleeding disorder with an estimated prevalence o...
Aging with rare bleeding disorders such as factor VII (FVII) deficiency poses several challenges to ...
We performed a prospective study of FVII inhibitor occurrence in a large number of patients with FV...
Activated factor VII (FVIIa), the first protease of clotting, expresses its physiological procoagula...
Factor VII deficiency is a rare bleeding disorder showing an autosomal recessive pattern of inherita...
Inherited factor VII (FVII) deficiency is a rare autosomal recessive disorder associated with a blee...
Patients with inherited factor VII (FVII) deficiency display different clinical phenotypes requiring...
Background: Inherited factor VII (FVII) deficiency is the most common among rare congenital bleeding...
The complex formed between the procoagulant serine protease activated factor VII (FVII) and the memb...
The complex formed between the procoagulant serine protease activated factor VII (FVII) and the memb...
Individuals with inherited factor VII (FVII) deficiency display bleeding phenotypes ranging from mil...
Aim: Factor VII deficiency is one of the hereditary coagulation disorders that has autosomal reccess...
BackgroundIn congenital Factor (F) VII deficiency bleeding phenotype and intrinsic FVII activity lev...
Factor VII deficiency is the most common among rare inherited autosomal recessive bleeding disorders...
Analysis of biological phenotypes from 42 patients with inherited factor VII deficiency: can biologi...
: Congenital factor VII (FVII) deficiency is a rare bleeding disorder with an estimated prevalence o...
Aging with rare bleeding disorders such as factor VII (FVII) deficiency poses several challenges to ...
We performed a prospective study of FVII inhibitor occurrence in a large number of patients with FV...
Activated factor VII (FVIIa), the first protease of clotting, expresses its physiological procoagula...
Factor VII deficiency is a rare bleeding disorder showing an autosomal recessive pattern of inherita...