Thalassaemia is a common hereditary haemolytic anaemia. Mild cases of this disease may
be asymptomatic, while patients with severe thalassaemias require high-dose blood …

To reduce anemia rates, it is crucial to gain a deeper understanding of anemia and its
associated factors. It is essential for teenagers who are going through a period of rapid …

目的: 建立一种快速, 简便且无需核酸提取的泰国型α 缺失地中海贫血的快速基因诊断方法及其
在产前诊断中应用. 方法: 设计可以扩增α-珠蛋白基因簇中--THAI 等位基因的特征序列引物组 …

Background: The most common causes of microcytic hypochromic anemia are thalassemia
trait (TT) and iron deficiency anemia (IDA). Clinically, the differential diagnosis of TT and IDA …

Background: alpha-Thalassemia is caused primarily by deletions of one to two alpha-globin
genes and is characterized by absent or deficient production of alpha-globin protein. The …

BACKGROUND: Being located in the global thalassemia belt area, Indonesia is estimated
harboring about 10% thalassemia carriers; however, screening program is still diversely …

Background Thalassemia is a monogenic, autosomal recessive, inherited disorder of the red
blood cells caused by mutations or deletions in the globin gene. Approximately 6–10% of …

This study introduces an innovative paradigm for Alpha thalassemia detection by integrating
machine learning, hyperparameter tuning, and explainable artificial intelligence (XAI) …

An effective way of learning about thalassemia, a complex public health issue with multiple
perspectives, is through participating in research. This study used an inductive approach to …

O objetivo do presente estudo foi analisar o Índice de Mentzer como adjuvante no
diagnóstico do traço talassêmico da beta-talassemia, visto que, na sua forma homozigota a …