Background Regularly transfused people with sickle cell disease (SCD) and people with
thalassaemia (who are transfusion‐dependent or non‐transfusion‐dependent) are at risk of …

Few studies have investigated the quality of life of children with thalassemia in the Middle
East or Mediterranean region, especially Iraq. Therefore, this study was performed to assess …

Patient-reported outcome measures (PROMs) are questionnaires completed by patients or
caregivers without influence by health care professionals. As such, PROMs show subjective …

The β-thalassemias and sickle cell disorders pose a major health burden in the large and
diverse Indian population. Education programs for awareness generation are being done by …

The clinical presentation of HbE-β-thalassemia is extremely variable, however, many cases
are severe and transfusion dependent. We offered prenatal diagnosis to 108 couples, 20 of …

Background The recommendations of this article are based in part upon work in the
thalassemias, inherited disorders of hemoglobin that are widely prevalent in Asia, which …

Background Regularly transfused people with sickle cell disease (SCD) and people with
thalassaemia are at risk of iron overload. Iron overload can lead to iron toxicity in vulnerable …

Few studies have investigated the quality of life of children with thalassemia in the Middle
East or Mediterranean region, especially Iraq. Therefore, this study was performed to assess …

Abstract Introduction: Molecular screening of Thalassemia is a burning issue especially for
developing country where birth rate is high and most of the victims are from rural and from …

ABSTRACT Introduction: Molecular screening of Thalassemia is a burning issue especially
for developing country where birth rate is high and most of the victims are from rural and …