Objectives: To evaluate the use of magnetic resonance imaging inpatients with β-thalassemia and to compare T2* magnetic resonanceimaging results with serum ferritin levels and the redox active fraction of labile plasma iron. Methods: We have retrospectively evaluated 115 chronically transfused patients (65 women). We tested serum ferritin with chemiluminescence, fraction of labile plasma iron by cellular fluorescence and used T2* MRI to assess iron content in the heart, liver, and pancreas. Hepatic iron concentration was determined in liver biopsies of 11 patients and the results were compared with liver T2* magnetic resonance imaging. Results: The mean serum ferritin was 2,676.5 +/- 2,051.7 ng/mL. A fraction of labile plasma iron was abnor...
Background: Cardiac failure secondary to transfusional iron overload is the most common cause of dea...
Cardiac involvement in patients with thalassemia intermedia (TI) is characterized by a high-output s...
OBJECTIVE: To identify predictive variables of iron overload in patients with sickle cell anemia, co...
Purpose: This study aimed to evaluate iron levels in cardiac and hepatic tissues using magnetic reso...
The patients of thalassaemia major need repeated blood transfusion which leads to excess iron deposi...
Objective This study was performed to assess cardiac and hepatic iron overload in young patients wit...
Aim of the study: The aim of this study was to assess the utility of MRI as a non-invasive technique...
Objective: Cardiac T2* magnetic resonance imaging (MRI) has recently attracted considerable attentio...
AbstractPatients with chronic hemolytic anemia like thalassemia and sickle cell anemia need repeated...
Purpose: To assess the correlation between MRI findings of the pancreas with those of the heart and ...
Introduction: In this study, we aimed to assess the relationship of cardiac and hepatic T2* magnetic...
Abstract Background Thalassemia is the most prevalent single-gene disorder. Myocardial and hepatic i...
Accumulation of iron in thalassemia causes organ damage and reduces patient survival due to heart le...
Thalassemia is a genetic disease caused by disruption of globin chain synthesis leading to severe an...
Iron can be deposited in all internal organs, leading to different types of functional abnormalities...
Background: Cardiac failure secondary to transfusional iron overload is the most common cause of dea...
Cardiac involvement in patients with thalassemia intermedia (TI) is characterized by a high-output s...
OBJECTIVE: To identify predictive variables of iron overload in patients with sickle cell anemia, co...
Purpose: This study aimed to evaluate iron levels in cardiac and hepatic tissues using magnetic reso...
The patients of thalassaemia major need repeated blood transfusion which leads to excess iron deposi...
Objective This study was performed to assess cardiac and hepatic iron overload in young patients wit...
Aim of the study: The aim of this study was to assess the utility of MRI as a non-invasive technique...
Objective: Cardiac T2* magnetic resonance imaging (MRI) has recently attracted considerable attentio...
AbstractPatients with chronic hemolytic anemia like thalassemia and sickle cell anemia need repeated...
Purpose: To assess the correlation between MRI findings of the pancreas with those of the heart and ...
Introduction: In this study, we aimed to assess the relationship of cardiac and hepatic T2* magnetic...
Abstract Background Thalassemia is the most prevalent single-gene disorder. Myocardial and hepatic i...
Accumulation of iron in thalassemia causes organ damage and reduces patient survival due to heart le...
Thalassemia is a genetic disease caused by disruption of globin chain synthesis leading to severe an...
Iron can be deposited in all internal organs, leading to different types of functional abnormalities...
Background: Cardiac failure secondary to transfusional iron overload is the most common cause of dea...
Cardiac involvement in patients with thalassemia intermedia (TI) is characterized by a high-output s...
OBJECTIVE: To identify predictive variables of iron overload in patients with sickle cell anemia, co...