22 results on '"Reitsma PH"'
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2. Apparent different thrombotic tendency in patients with factor V Leiden and protein C deficiency due to selection of patients
3. A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
4. Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor
5. Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients
6. Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients
7. Protein C deficiency in a controlled series of unselected outpatients: an infrequent but clear risk factor for venous thrombosis (Leiden Thrombophilia Study) [see comments]
8. High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance) [see comments]
9. Hereditary antithrombin deficiency: heterogeneity of the molecular basis and mortality in Dutch families
10. Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families
11. Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families
12. Hemophilia B Leyden: substitution of thymine for guanine at position - 21 results in a disruption of a hepatocyte nuclear factor 4 binding site in the factor IX promoter
13. The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects
14. The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects
15. Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460
16. Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460
17. Two novel point mutations correlate with an altered developmental expression of blood coagulation factor IX (hemophilia B Leyden phenotype)
18. The putative factor IX gene promoter in hemophilia B Leyden
19. Partial protein S gene deletion in a family with hereditary thrombophilia
20. Partial protein S gene deletion in a family with hereditary thrombophilia
21. Two novel point mutations correlate with an altered developmental expression of blood coagulation factor IX (hemophilia B Leyden phenotype)
22. The putative factor IX gene promoter in hemophilia B Leyden
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