Beta (β)‐thalassemia and sickle cell disease (SCD) are characterized by a hypercoagulable
state, which can significantly influence organ complication and disease severity. While red …

β-Thalassemia especially transfusion-dependent thalassemia (TDT) associates with a
hypercoagulable state, which is the main cause of thromboembolic events (TEE). Plasma …

Patients with transfusion-dependent β-thalassemia (TDT) with iron overload have been
linked to hypercoagulability and increased platelet (PLT) activation that causes thrombosis …

This study was conducted to assess the level of proteins C and S in patients with
thalassemia intermedia from the Thalassemia Center in Erbil, Iraq. This study aimed to …

Background β-thalassemia is a group of inherited blood disorders that affect the production
of β-globin chains, leading to the reduction or absence of these chains. One of the …

BACKGROUND: Thromboembolic (TE) disorders are among the most common
complications of beta-thalassemia. We designed this cross-sectional study to investigate the …

Hypercoagulability and increased platelet activation have been associated with iron-
overloaded β− thalassemia patients resulting in thrombosis. Iron chelators, antiplatelet and …

Beta thalassemia is a prevalent form of hereditary haemolytic anaemia that is frequently
observed in the Mediterranean region. The prevalence of thromboembolism among patients …

Results: The mean protein C values in non-splenectomized and splenectomized patients
were 62.11±9.65% and 41.64±6.37% respectively with a significant difference by …

Despite some major improvements in treating beta thalassemia in the past, it remains a
challenge to avoid the various complications which go along with iron overload. We …