Objective: Unlike beta thalassemia major (β-TM) in which cardiac siderosis represents the leading cause of mortality and morbidity, in beta thalassemia intermedia (β-TI), pulmonary hypertension (PHT) and thrombosis seems to be the major cardiovascular complications. However, the mechanism underlying these complications in β-TI is still unclear. Endothelial dysfunction, the key early event in atherogenesis, is now emerging as an important cardiovascular risk determiner in β-TI patients. Among the factors known to affect endothelial function, iron and cholesterol merit particular consideration in β-TI patients. Therefore, with the aim to extend our knowledge on the mechanisms connecting atherosclerosis to β-TI, in this study, we compared ...
<div><p>Human β-thalassemia major is one of the most prevalent genetic diseases characterized by dec...
BACKGROUND: Pulmonary hypertension (PHT) is a common yet poorly understood complication of \u3b2 tha...
In plasma, iron is normally bound to transferrin, the principal protein in blood responsible for bin...
Introduction. Cardiovascular involvement represents a well-known complication and the primary cause ...
In thalassemia major, pancreatic iron was demonstrated as a powerful predictor not only for the alte...
In thalassemia major, pancreatic iron was demonstrated as a powerful predictor not only for the alte...
BACKGROUND: Beta-thalassemia major is associated with increased cardiovascular risk, although the un...
Background Patients with \u3b2 thalassemia intermedia can have substantial iron overload, irrespecti...
International audienceCardiac involvement in patients with thalassemia intermedia (TI) is characteri...
Although the presence of nontransferrin bound plasma Iron (NTBI) in transfusional iron overload is w...
Cardiac involvement in patients with thalassemia intermedia (TI) is characterized by a high-output s...
Background and aim: Notwithstanding the improvement in therapies, patients affected by thalassemia ...
Heart disease is the leading cause of mortality and one of the main causes of morbidity in beta-thal...
Although pulmonary function abnormalities in thalassaemia major (TM) were described in 1980, the pat...
OBJECTIVES: The occurrence of cardiac iron deposition is one of the late effect of iron over load wh...
<div><p>Human β-thalassemia major is one of the most prevalent genetic diseases characterized by dec...
BACKGROUND: Pulmonary hypertension (PHT) is a common yet poorly understood complication of \u3b2 tha...
In plasma, iron is normally bound to transferrin, the principal protein in blood responsible for bin...
Introduction. Cardiovascular involvement represents a well-known complication and the primary cause ...
In thalassemia major, pancreatic iron was demonstrated as a powerful predictor not only for the alte...
In thalassemia major, pancreatic iron was demonstrated as a powerful predictor not only for the alte...
BACKGROUND: Beta-thalassemia major is associated with increased cardiovascular risk, although the un...
Background Patients with \u3b2 thalassemia intermedia can have substantial iron overload, irrespecti...
International audienceCardiac involvement in patients with thalassemia intermedia (TI) is characteri...
Although the presence of nontransferrin bound plasma Iron (NTBI) in transfusional iron overload is w...
Cardiac involvement in patients with thalassemia intermedia (TI) is characterized by a high-output s...
Background and aim: Notwithstanding the improvement in therapies, patients affected by thalassemia ...
Heart disease is the leading cause of mortality and one of the main causes of morbidity in beta-thal...
Although pulmonary function abnormalities in thalassaemia major (TM) were described in 1980, the pat...
OBJECTIVES: The occurrence of cardiac iron deposition is one of the late effect of iron over load wh...
<div><p>Human β-thalassemia major is one of the most prevalent genetic diseases characterized by dec...
BACKGROUND: Pulmonary hypertension (PHT) is a common yet poorly understood complication of \u3b2 tha...
In plasma, iron is normally bound to transferrin, the principal protein in blood responsible for bin...