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MRI evaluation of tissue iron burden in patients with β-thalassaemia major

β-Thalassaemia major is a hereditary haemolytic anaemia that is treated with multiple blood transfusions. A major complication of this treatment is iron overload, which leads to cell death and organ dysfunction. Chelation therapy, used for iron elimination, requires effective monitoring of the body...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Argyropoulou, Maria I., Astrakas, Loukas
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Springer-Verlag 2007
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2292491/
https://ncbi.nlm.nih.gov/pubmed/17710390
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00247-007-0567-1
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