Laboratory Investigations of Thrombophilia, Gebunden

Blurb

1. An Overview of Laboratory Diagnosis of Thrombophilia.- 2. Laboratory Diagnosis of Congenital Antithrombin Deficiency.- 3. Laboratory Diagnosis of Congenital and Acquired Protein C Deficiencies and Assays for Circulating Activated Protein C levels.- 4. Laboratory Diagnosis of Hereditary and Acquired Protein S Deficiencies.- 5. Laboratory Diagnosis of Protein Z Deficiency.- 6. Laboratory Diagnosis of Factor V Leiden.- 7. Laboratory Diagnosis of Prothrombin G20210A Mutation.- 8. Laboratory Diagnosis of Congenital and Acquired Hyper-homocysteinemia.- 9. Laboratory Diagnosis of Congenital Plasminogen Deficiency.- 10. Laboratory Diagnosis of Congenital Tissue Factor Pathway Inhibitor.- 11. Laboratory Diagnosis of Tissue Plasminogen Activator Deficiency.- 12. Laboratory Diagnosis of Combined Inherited / Genetic Thrombophilia.- 13. Laboratory Diagnosis of Inherited and Acquired Factors Involved in Thrombosis.