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Factor VIII inhibitors in patients with congenital severe haemophilia A and its relation to genotype
(Wiley Online Library, 2015)
Genetic Variations In Sites Of Affinity Between Fviii And Lrp1 Are Not Associated With High Fviii Levels In Venous Thromboembolism
(NATURE PUBLISHING GROUPLONDON, 2015)
Molecular Genetic Testing of Hemostasis and Thrombosis in Developing Countries: Achievements, Hopes, and Challenges
(Thieme Medical Publ IncNew YorkEUA, 2008)
Analysis of Factor VIII polymorphic markers as a means for carrier detection in Brazilian families with haemophilia A
(Blackwell Publishing, 2007-07-01)
Haemophilia A is an X-linked, recessively inherited bleeding disorder of varying severity, which results from the deficiency of procoagulant factor VIII f(8). Linkage diagnosis using polymorphic markers in the f8 gene is ...
Analysis of Factor VIII polymorphic markers as a means for carrier detection in Brazilian families with haemophilia A
(Blackwell Publishing, 2007-07-01)
Haemophilia A is an X-linked, recessively inherited bleeding disorder of varying severity, which results from the deficiency of procoagulant factor VIII f(8). Linkage diagnosis using polymorphic markers in the f8 gene is ...
Polymorphisms and Mutations in vWF and ADAMTS13 Genes and Their Correlation With Plasma Levels of FVIII and vWF in Patients With Deep Venous Thrombosis
(Sage Publications IncThousand OaksEUA, 2011)