Iron is an essential mineral that serves as a prosthetic group for a variety of proteins involved
in vital cellular processes. The iron economy within humans is highly conserved in that there …

Indonesia is located along the 'Thalassemia Belt'and a hotspot for hemoglobinopathies.
Around 3.0–10.0% of the population carry β-thalassemia (β-thal) and 2.6–11.0% of the …

Study background Thalassemia is the commonest genetic blood disorder in Malaysia which
requires life-long blood transfusions. From a total of 7,984 thalassemia patients in Malaysia …

Iron overload is a concern for patients who require repeated red-blood-cell transfusions due
to conditions such as sickle cell disease, thalassemia, or myelodysplastic syndromes. The …

This is the first report of successful deferasirox administration, using graded challenge and
treating through, in a patient with mild immediate hypersensitivity reaction. Beginning with …

A 33-year-old male presenting with subacute abdominal pain was found to have
hyperbilirubinaemia, hypokalaemia and hyponatraemia. This was in the setting of …

In this study, data from 171 patients with thalassemia were analyzed. There was high
variability in ferritin levels among patients, with a median of 2290 ng/mL. The median …

Objective: To assess the status of beta thalassemia disease in fetuses of beta thalassemia
carrier mothers and to determine the fate of these fetuses. Study Design: A cross sectional …

The MDS are clonal hematopoietic stem cell disorders characterized by ineffective
hematopoiesis, leading to peripheral blood cytopenias, red blood cell and platelet …

Introduction Methods Results Conclusions References Acknowledgments Disclosure Statement
Page 1 New Film-Coated Tablet Formulation of Deferasirox is Well Tolerated in Patients With …