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

Objective: This study aims to examine markers of coagulation activation and their possible
clinical associations in sickle cell disease (SCD) and thalassemia. Materials And Methods …

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 …

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: Sickle cell disease (SS), is one of the most common inherited hematologic
disorders, presents with chronic hemolytic anemia that can be punctuated by crises, infarcts …

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

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 …

It has been well-described that sickle cell disease (SCD) due to HbSS or HbSC is
associated with systemic activation of coagulation. A single study has reported a similar …

Background: Sickle cell disease (SCD) is an inherited blood disorder that affects red blood
cells.(SCD) is characterized by re-current vaso-occlusive crisis (VOC). Material and …