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Mutations in the MCFD2 genemay causeFactor V and Factor VIII combined deficiency
Hemophilia A ... a X - linked recessive hereditary clotting factor deficiency conditionleadto decreased factor VIII activity
A ... a X - linked hereditary conditionleadto decreased factor VIII activity
the basisdid ... inventhuman Factor VIII : C
mutations(passive) is caused bydeficiency of Factor V and Factor VIII
The absence of von Willebrand factorcausesfactor VIII to be less stable
mutations in the F7 gene knownto causeFactor VII disorder
a genetic mutation in factor VII production resulting in reduced factor VII activity(passive) is caused by Factor VIII deficiency
a genetic mutation in factor VII production resulting in reduced factor VII activity(passive) is caused byFactor VIII deficiency
variants in the gene that codes for coagulation factor VII(passive) is caused byFactor VII deficiency
by a deficiency or defect in the clotting protein(passive) is ... caused byFactor IX deficiency
Factorsinfluencingfactor VIII activity
a problem with factor VII(passive) is caused byFactor VII deficiency
an X - linked recessive disordercausesfactor VIII deficiency
novel mutation mechanismsleadingto factor VIII deficiency
a change , or mutation(passive) is caused byFactor IX Deficiency
by an inhibitory antibody to factor viii(passive) caused byfactor viii deficiency
an inhibitory antibody to factor VIII(passive) caused byfactor VIII deficiency
This test ... knownto causeFactor VII deficiency
by a promoter mutation(passive) caused byfactor VII deficiency
desmopressincausesrelease of factor VIII
any drugcausingFACTOR VIII DEFICIENCY
other drugscauseFACTOR VIII DEFICIENCY
by the methods(passive) designed byhuman Factor VIII
the basisdid ... inventhuman Factor VIII
a structural variant N57D of the first epidermal growth factor domain(passive) caused byFactor VII deficiency
by a structural variant N57D of the first epidermal growth factor(passive) caused byFactor VII deficiency
other drugscauseFACTOR VIII INHIBITION
mutationscausingfactor VIII assay
by metal - induced oxidation(passive) is causedFactor VIII inactivation
by metal - induced oxidation(passive) is caused byFactor VIII inactivation
a deficiency of factor VIII(passive) is caused byFactor VIII concentrate and cryoprecipitate
of 20 homologous domains(passive) is composedFactor H
a deficiency of clotting factor IX(passive) is caused byFactor IX concentrate
of 20 repetitive modules of approximately about 60 amino acids , the Short Consensus Repeat ( SCR ) which forms a flexible structure(passive) is composedFactor H
factor IX geneleadingto factor VIII
the Factor VIII complexresultsin the Factor VIII
to the average concentration of the measured factors(passive) was setFactor IX
mutationscausingfactor VII
a defective geneleadingto factor VIII
hemophiliacauseshemophilia
an inherited X - linked disease(passive) caused byan inherited X - linked disease
The disorder is mainly an inherited deficiency of the Factor VIII geneCausesThe disorder is mainly an inherited deficiency of the Factor VIII gene
a hematological disorder(passive) caused bya hematological disorder
Factor VIII deficiency ( choice A ) , or hemophilia A(passive) is caused byFactor VIII deficiency ( choice A ) , or hemophilia A
severe hemophiliacausingsevere hemophilia
to severe hemophilia Aleadingto severe hemophilia A
to abnormal bleedingleadingto abnormal bleeding
hemophiliacausinghemophilia
an X - linked recessive disease , usually inherited and affecting primarily males(passive) caused byan X - linked recessive disease , usually inherited and affecting primarily males
hemophilia Acauseshemophilia A
in hemophilia Aresultsin hemophilia A
Combined factor V and(passive) is causedCombined factor V and
Hemophilia A ( classic hemophilia(passive) is caused byHemophilia A ( classic hemophilia
to insufficient fibrin formationleadsto insufficient fibrin formation
haemophilia A(passive) is caused byhaemophilia A
a prolonged aPTTto causea prolonged aPTT
excessive and sometimes fatal bleeding from minor wounds and surgerycausesexcessive and sometimes fatal bleeding from minor wounds and surgery
to deficiency in Factor VIIIleadsto deficiency in Factor VIII
increased clotting and cerebral venous thrombosiscan causeincreased clotting and cerebral venous thrombosis
in greatly enhanced factor VIII activityresultsin greatly enhanced factor VIII activity
in greatly enhanced factor VIII activityresultsin greatly enhanced factor VIII activity
the one - stage prothrombin timeinfluencethe one - stage prothrombin time
a nasty case X - linked Haemophilia B in her male descendants ( a mutation that was only mapped in 2009 by sequencing the bones of the murdered Romanov branchcauseda nasty case X - linked Haemophilia B in her male descendants ( a mutation that was only mapped in 2009 by sequencing the bones of the murdered Romanov branch
A non - genetic form of haemophilia(passive) is caused byA non - genetic form of haemophilia
in decreased levels of coagulation factor VIIIresultingin decreased levels of coagulation factor VIII
What blood disorder(passive) is caused byWhat blood disorder
a rare bleeding disorder(passive) caused bya rare bleeding disorder
increased bleeding and usually affects malescausesincreased bleeding and usually affects males
a bleeding disorder(passive) caused bya bleeding disorder
a severe bleeding disorder(passive) caused bya severe bleeding disorder
in poor responseresultsin poor response
in low factor VIII levels and bleeding patterns similar to those seen in the hemophiliasresultingin low factor VIII levels and bleeding patterns similar to those seen in the hemophilias
thrombin elevation(passive) caused bythrombin elevation
increased bleedingcausesincreased bleeding
from a congenital deficiency or absence of factor IXalso resultsfrom a congenital deficiency or absence of factor IX
in abnormal bleedingresultingin abnormal bleeding
bleeding in patients with factor levels less than 1 percent ( normal is greater than 50 percentcan causebleeding in patients with factor levels less than 1 percent ( normal is greater than 50 percent
hemophilia B.causeshemophilia B.
hemophilia A.causeshemophilia A.