Abstract Background Aims: Hepcidin is low in β-thalassemia patients, suggesting a critical
role in iron accumulation. Hepcidin has not been assessed in Jordanian thalassemia …

This work was carried out to investigate the role of Glutathione S-Transferase M1 (GSTM1)
null genotype frequency in prognosis of β-thalassemia, and to detect the correlation …

In children with β-thalassemia (β-thal) trait, tissue damage occurs with oxidative stress due
to oxygen free radicals and reactive oxygen species (ROS) production. Dynamic thiol …

Fish species from the Red Sea constitute an excellent food source but are also unsafe to
consume because their content of iron (Fe) is greater than the recommended level. We …

Пациентите с БТМ са изложени на значителен оксидативен стрес, вследствие на
железен свръхтовар. Свободните радикали окисляват различни клетъчни компоненти …

Background: Beta-thalassemia is a genetic disorder characterized by either a reduced or
deficiency of β-globin chain which results in imbalance of α-globin chains and red cell …

Objectives: to evaluate Pentraxin-3 Levels (PTX-3) in pediatric patients with β-thalassemia
major, intermedia and minor and its relationship with antioxidant capacity and total oxidant …

Objective: It is aimed to investigate the underlying causes of thalassemia, which has
widespread and negative effects around the world, and to create solutions. For this purpose …

Introduction: Patients with b-thalassemia major (b-TM) are at risk of developing abnormal
lipid profiles. Lipid abnormalities, in turn, have a potential role in the pathogenesis of some …

摘要目的: 探讨海兔素对刀豆蛋白A 诱导的化学性肝损伤保护作用. 方法: 雄性Wistar
大鼠随机分为4 组. 模型组与海兔素组给予15 mg/kg 刀豆蛋白A 尾静脉注射每周一次 …