Juvenile dermatomyositis (JDM) is a rare autoimmune disease mainly characterized by
muscle and skin involvement. Vasculopathy is considered central to the pathogenesis of the …

Sickle cell disease (SCD) is the most common hereditary disease worldwide, presenting
with anemia and intermittent severe pain. Pregnancy in a patient with SCD is associated …

Circulating endothelial cells (CEC) and endothelial microparticles (EMP) are emerging as
markers of endothelial repair and activation/apoptosis. Although significant changes in the …

It is highly expected that COVID-19 infection will have devastating consequences in sickle
cell disease (SCD) patients due to endothelial activation and decreased tissue and organ …

Sickle cell disease (SCD), one of the most common genetic disorders worldwide, is
characterized by hemolytic anemia and tissue damage from the rigid red blood cells …

Aims: High mobility group box 1 (HMGB1) is a DNA-binding protein secreted into the
extracellular space from necrotic cells that acts as a cytokine. We examined the role of …

The article presents a study which analyzed the presence of JAK2< sup> V617F-positive
myeloproliferative neoplasm (JAK2< sup> V617F MPN) in patients with Budd-Chiari …

Aims: Alpha-2-macroglobulin (α2 MG) is thought to be associated with inflammatory
reactions and procoagulant properties that might cause ischemic stroke. Endothelial …

Adult patients with sickle cell disease (SCD) are highly susceptible to stem cell transplant
complications, including drug toxicity, graft versus host disease (GVHD), and graft rejection …

Sickle cell disease (SCD) is a devastating hemolytic disease, marked by recurring bouts of
painful vaso-occlusion, leading to tissue damage from ischemia/reperfusion …