Haemostatic disorders in sickle cell disease subjects in Nigeria: A review of literature
Background: Sickle cell disease (SCD) is an autosomal recessive disorder that is
characterised with chronic anaemia and painful crisis. SCD is associated with …
characterised with chronic anaemia and painful crisis. SCD is associated with …
Protein C and antithrombin levels in patients with sickle cell anemia in Ahmadu Bello University Teaching Hospital Zaria
Background: Alterations in the components of hemostasis, namely platelet function, the
procoagulant, anticoagulant, and the fibrinolytic systems, are observed in sickle cell anemia …
procoagulant, anticoagulant, and the fibrinolytic systems, are observed in sickle cell anemia …
[PDF][PDF] Symmetric Peripheral Gangrene (SPG) of Four Limbs in a Child with Sickle Cell Anemia
AS Umar, A Halima - saspublishers.com
Sickle cell disease (SCD) is the most common genetic disorder in the world, which has a
varied clinical manifestations and severity. Vascular thrombosis leading to symmetrical …
varied clinical manifestations and severity. Vascular thrombosis leading to symmetrical …