Study of gonadal hormones in Egyptian female children with sickle cell anemia in correlation with iron overload: Single center study
Objective/Background: Sickle cell disease is a hereditary hemoglobinopathy characterized by abnormal hemoglobin production, hemolytic anemia, and intermittent occlusion of small blood vessels, leading to tissue ischemia, chronic organ damage, and organ dysfunction including endocrine organs. The aim...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Medknow Publications
2016-01-01
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| coleção: | Hematology/Oncology and Stem Cell Therapy |
| Assuntos: | |
| Acesso em linha: | https://journals.lww.com/10.1016/j.hemonc.2015.11.005 |
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