Thromboembolic events are a significant clinical concern in thalassemia and
hemoglobinopathies, highlighting the need for new strategies to treat and detect these …

ABSTRACT Objectives: Beta-thalassemia (β-thal) is one of the most common genetic
disorders worldwide. Multiple genetic and epigenetic mechanisms could be implicated in the …

Southeast Asian ovalocytosis (SAO) is characterized by the misfolding of band 3 protein in
red blood cells (RBC). The abnormal structure of the band 3 protein results in dysmorphic …

Splenectomised β‐thalassaemia/haemoglobin E (HbE) patients have increased levels of
circulating microparticles or medium extra‐cellular vesicles (mEVs). The splenectomised …

Objective To determine the number and intensity of phosphatidylserine (PS) expression of
the red blood cells (RBCs), fragmented RBCs, and RBC-derived microparticles (RMPs) in …

Thalassemia disease is a common inherited hemolytic anemia frequently found in several
parts of the world, especially in the Mediterranean and some Asian countries. Besides the …

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 …

In the last few decades, the prognosis of patients with β-thalassemia has improved
dramatically. However these patients suffer from many serious complications. One of the …

Increased levels of circulating platelet microparticles as a... : The Egyptian Journal of
Haematology Increased levels of circulating platelet microparticles as a risk of hypercoagulable …

Микровезикулы-это гетерогенная группа внеклеточных частиц, образуемых
различными типами клеток при активации или апоптозе, играющих важную, а порой …