Some properties of a new congenital abnormality of the prothrombin molecule are described. In the propositus' plasma, the prothrombin level is half normal plasma concentration estimated in the one and two stage test and in the staphylocoagulase assay but it is in the normal range by the immunochemical assay. This abnormal prothrombin is modified during coagulation into a form that enables it to react with staphylocoagulase but not with prothrombinase. The immunoelectrophoresis of the serum reveals an abnormal pattern. The defect is found in one of the propositus' brothers. © 1974.SCOPUS: ar.jinfo:eu-repo/semantics/publishe
Adequate classifications of disorders are of paramount importance in the management of congenital bl...
thrombosis over the last 15 yr has been investigated. The only abnormality found in this patient was...
Until recently the laboratory diagnosis of thrombophilia consisted on investigation of the plasmatic...
Prothrombin deficiency is among the rarest inherited coagulation disorders, with a prevalence of app...
The propositus is a 4-year-old boy who presented with a history of excessive bleeding after surgical...
thrombosis was studied to determine if a plasma pro-tein deficiency could account for the observed d...
Normal blood coagulation is a complex process, involving a cascade of activation of different plasma...
Prothrombin deficiency is a very rare disorder caused by mutations in the F2 gene that generate hypo...
Factor VII (FVII) deficiency is one of the two congenital coagulation disorders that was not discove...
Congenital prothrombin deficiency is one of the rarest clotting disorders. It is commonly subdivided...
Recently several variants of clotting factors have shown a peculiar behavior so that they appear as ...
Prothrombin deficiency is an autosomal recessive disorder associated with a moderately severe bleedi...
The molecular bases of congenital thrombophilias and of its life-threatening complication, polmonary...
Abstract: A heterozygous G-->T transversion at position 1388 of the protein C (PC) gene which predi...
Four members of an Italian family (two with histories of venous thromboembolism) had a qualitative d...
Adequate classifications of disorders are of paramount importance in the management of congenital bl...
thrombosis over the last 15 yr has been investigated. The only abnormality found in this patient was...
Until recently the laboratory diagnosis of thrombophilia consisted on investigation of the plasmatic...
Prothrombin deficiency is among the rarest inherited coagulation disorders, with a prevalence of app...
The propositus is a 4-year-old boy who presented with a history of excessive bleeding after surgical...
thrombosis was studied to determine if a plasma pro-tein deficiency could account for the observed d...
Normal blood coagulation is a complex process, involving a cascade of activation of different plasma...
Prothrombin deficiency is a very rare disorder caused by mutations in the F2 gene that generate hypo...
Factor VII (FVII) deficiency is one of the two congenital coagulation disorders that was not discove...
Congenital prothrombin deficiency is one of the rarest clotting disorders. It is commonly subdivided...
Recently several variants of clotting factors have shown a peculiar behavior so that they appear as ...
Prothrombin deficiency is an autosomal recessive disorder associated with a moderately severe bleedi...
The molecular bases of congenital thrombophilias and of its life-threatening complication, polmonary...
Abstract: A heterozygous G-->T transversion at position 1388 of the protein C (PC) gene which predi...
Four members of an Italian family (two with histories of venous thromboembolism) had a qualitative d...
Adequate classifications of disorders are of paramount importance in the management of congenital bl...
thrombosis over the last 15 yr has been investigated. The only abnormality found in this patient was...
Until recently the laboratory diagnosis of thrombophilia consisted on investigation of the plasmatic...