Application of modern and innovative spectroscopic and microscopic approaches to
biomedical analysis opens new horizons and sheds new light on many unexplored scientific …

β-thalassaemia is a rare genetic condition caused by mutations in the β-globin gene that
result in severe iron-loading anaemia, maintained by a detrimental state of ineffective …

In Guangxi, Hainan, and Fujian Province in southern China, β-thalassemia is a frequent
monogenic hereditary disorder that is primarily defined by hemolytic anemia brought on by …

Silica nanoparticles (SiNPs) have attracted increasing attention for their health effects due to
the increased risk of exposure to human bodies via diverse routes. Considering that SiNPs …

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

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 …

Abstract β-Thalassemia (β-thal), is an inherited blood disorder caused by reduced or absent
synthesis of β-globin chains leading to imbalance of globin chain synthesis. The clearance …

Abstract Background/Aim: It is not known why cerebrovascular and cardiovascular
ischaemic events are less frequently observed in heterozygous beta thalassaemia (HBT) …

Bone marrow transplantation (BMT) serves as the only curative treatment for patients with β-
thalassemia major; however, hemostatic changes have been observed in these BMT …

Moyamoya is an occlusive vasculopathy characterized by progressive bilateral or unilateral
stenosis/occlusion of the distal internal carotid artery and the abnormal development of a …