Cargando…
Non-invasive MRI biomarkers for the early assessment of iron overload in a humanized mouse model of β-thalassemia
β-thalassemia (βT) is a genetic blood disorder causing profound and life threatening anemia. Current clinical management of βT is a lifelong dependence on regular blood transfusions, a consequence of which is systemic iron overload leading to acute heart failure. Recent developments in gene and chel...
Autores principales: | Jackson, Laurence H., Vlachodimitropoulou, Evangelia, Shangaris, Panicos, Roberts, Thomas A., Ryan, Thomas M., Campbell-Washburn, Adrienne E., David, Anna L., Porter, John B., Lythgoe, Mark F., Stuckey, Daniel J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5327494/ https://www.ncbi.nlm.nih.gov/pubmed/28240317 http://dx.doi.org/10.1038/srep43439 |
Ejemplares similares
-
Residual erythropoiesis protects against myocardial hemosiderosis in transfusion-dependent thalassemia by lowering labile plasma iron via transient generation of apotransferrin
por: Garbowski, Maciej W., et al.
Publicado: (2017) -
Brain iron content in systemic iron overload: A beta-thalassemia quantitative MRI study
por: Manara, Renzo, et al.
Publicado: (2019) -
Treating thalassemia major-related iron overload: the role of deferiprone
por: Berdoukas, Vasilios, et al.
Publicado: (2012) -
β-Thalassemia: HiJAKing Ineffective Erythropoiesis and Iron Overload
por: Melchiori, Luca, et al.
Publicado: (2010) -
Myocardial iron overload in sickle/thalassemia patients of Italian origin
por: Meloni, Antonella, et al.
Publicado: (2013)