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Comparison of biventricular dimensions and function between pediatric sickle-cell disease and thalassemia major patients without cardiac iron
Patients with chronic anemia develop compensatory ventricular dilation, even when maintained on chronic transfusion regimens. It is important to characterize these effects to interpret pathological changes in cardiac dimensions and function introduced by iron overload and sickle cell vasculopathy. O...
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| Publicado no: | Am J Hematol |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6903699/ https://ncbi.nlm.nih.gov/pubmed/23386313 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajh.23376 |
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