Add to ORKGCongenital factor VII deficiency (FVIID) is a rare disorder with a wide range of bleeding manifestations. The disorder does not protect patients against occurrence of thrombosis, and deep vein thrombosis can occur in the setting of surgery and recombinant factor VIIa replacement
There has been wide variation in the reported haemorrhagic manifestations of factor VII deficiency. ...
The congenital deficiency of coagulation factor VII (FVII) (OMIM: 227500) is a rare hemorrhagic diso...
factor) is the plasma cofactor for the prothrombinase complex that activates prothrombin to thrombin...
Inherited factor VII (FVII) deficiency is considered to be a haemorrhagic disease. Nonetheless, some...
Thrombosis in congenital factor (F) VII deficiency was investigated through extensive phenotypic and...
The complex formed between the procoagulant serine protease activated factor VII (FVII) and the memb...
Adequate classifications of disorders are of paramount importance in the management of congenital bl...
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...
Factor VII (F VII) deficiency is a rare coagulation disorder inherited autosomal recessively. Accord...
Thrombosis has been occasionally described in congenital FVII deficiency. This report deals with pat...
Activated factor VII (FVIIa), the first protease of clotting, expresses its physiological procoagula...
Aim: Factor VII deficiency is one of the hereditary coagulation disorders that has autosomal reccess...
Background: The occurrence of a thrombotic event in congenital bleeding disorders has drawn consider...
Congenital factor VII deficiency is the most common form of rare coagulation factor deficiencies. Th...
There has been wide variation in the reported haemorrhagic manifestations of factor VII deficiency. ...
The congenital deficiency of coagulation factor VII (FVII) (OMIM: 227500) is a rare hemorrhagic diso...
factor) is the plasma cofactor for the prothrombinase complex that activates prothrombin to thrombin...
Inherited factor VII (FVII) deficiency is considered to be a haemorrhagic disease. Nonetheless, some...
Thrombosis in congenital factor (F) VII deficiency was investigated through extensive phenotypic and...
The complex formed between the procoagulant serine protease activated factor VII (FVII) and the memb...
Adequate classifications of disorders are of paramount importance in the management of congenital bl...
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...
Factor VII (F VII) deficiency is a rare coagulation disorder inherited autosomal recessively. Accord...
Thrombosis has been occasionally described in congenital FVII deficiency. This report deals with pat...
Activated factor VII (FVIIa), the first protease of clotting, expresses its physiological procoagula...
Aim: Factor VII deficiency is one of the hereditary coagulation disorders that has autosomal reccess...
Background: The occurrence of a thrombotic event in congenital bleeding disorders has drawn consider...
Congenital factor VII deficiency is the most common form of rare coagulation factor deficiencies. Th...
There has been wide variation in the reported haemorrhagic manifestations of factor VII deficiency. ...
The congenital deficiency of coagulation factor VII (FVII) (OMIM: 227500) is a rare hemorrhagic diso...
factor) is the plasma cofactor for the prothrombinase complex that activates prothrombin to thrombin...