Introduction: Sickle cell anemia (SCA) is one of the common hematological disorders found
worldwide. Determination of the difference between steady state and sickle cell crisis in term …

Background: Characterization of hematological parameters in patients with sickle cell
anemia can direct treatment goals toward strategies reducing morbidity and mortality rate …

Background: Reports from various studies showed that patients with sickle cell anemia
(SCA) have altered components of hemostasis such as platelet function, the procoagulant …

Background: Sickle cell anemia (SCA) is an emerging public health challenge in India as
well as globally. The WHO recognized it as a global problem since long time. In Western …

Aim This study aimed at determining the clinical and laboratory predictors of frequency of
painful VOC among SCA patients in Enugu, Southeastern Nigeria. Materials and Methods It …

BACKGROUND: Volume indices and count of platelets through sickle cell anemia (SCA)
steady state are modified by chronic hemolysis, red blood cell sickling, and vaso-occlusion …

Background: Sickle cell disease (SCD) is considered to be a hypercoagulable state that
contributes to the morbidity associated with the disease. Numerous mechanisms can …

Background: Sickle cell disease (SCD) is a hereditary haemoglobinopathy characterized by
deranged haematopoiesis, and intermittent occlusion of small blood vessels. Patients can …

Sickle cell disease (SCD) is an inherited condition characterized by chronic haemolytic
anaemia. SCD is associated with moderate to severe anaemia, hypercoagulable state and …

Background: The evidence from various studies showed that patients with sickle cell disease
(SCD) have altered components of hemostasis such as platelet function, procoagulant …