Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease beta-thalassemia
Comorbidity C0282193|iron overload
Sentences 15
PubMedID- 25671931 Comparison of deferiprone and deferrioxamine for the treatment of transfusional iron overload in children with beta thalassemia major.
PubMedID- 25922644 We recommend that regardless of the amount of iron overload in patients with beta thalassemia major that have shown some degree of fibrosis in their liver biopsy before transplantation, appropriate steps should be taken to reduce iron overload as soon as possible after successful transplantation.
PubMedID- 25601433 Genetic modifiers of secondary iron overload in beta thalassemia major.
PubMedID- 24790662 iron overload in beta thalassaemia major and intermedia patients.
PubMedID- 21791471 This study evaluates whether iron overload in patients with beta thalassemia intermedia is associated with morbidity.
PubMedID- 25161967 Background: diabetes mellitus is a major complication of iron overload in patients with beta thalassemia major.
PubMedID- 20383704 These results imply that combining the atrial ejection force index with the transmitral-derived echocardiographic assessment is a feasible way to detect early stages of myocardial iron overload in patients with beta thalassemia major.
PubMedID- 22645668 A study done on status of thyroid function and iron overload in patients with beta thalassemia major on deferoxamine in jordan concluded that there is significantly high (p < 0.05) levels of serum ferritin, ft3, zinc, and copper in patients with beta thalassemia major as compared to controls [13].
PubMedID- 23056717 Objective: dilated cardiomyopathy is the end result of chronic iron overload in patients with beta thalassemia major.
PubMedID- 25402221 The effects of deferasirox on renal haemodynamics, including glomerular filtration rate (gfr) and renal plasma flow (rpf), were investigated in a phase i, open-label study in beta thalassaemia major patients with iron overload.
PubMedID- 24575259 Background: frequent blood transfusion in patients with beta thalassemia major can lead to iron overload especially in liver.
PubMedID- 26205801 Objectives: 'the aim of this work was to compare the efficacy of different iron chelating agents' in the treatment of ' iron overload in children with beta thalassemia major'.
PubMedID- 19460052 Aims: to assess the significance of cardiac iron overload in patients with beta thalassaemia.
PubMedID- 19838709 This is the first study to prove the role of gst gene deletions with iron overload in hbe/beta thalassemia.
PubMedID- 25293426 Early heart iron overload in beta thalassemia major patients can be quantified through t2* cardiovascular magnetic resonance (cmr).

Page: 1