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Hemoglobin sickle cell disease complications: a clinical study of 179 cases
BACKGROUND: Hemoglobin sickle cell disease is one of the most frequent hemoglobinopathies. Surprisingly, few studies have been dedicated to this disease, currently considered to be a mild variant of homozygous sickle cell disease. The aim of this study was to update our knowledge about hemoglobin si...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Ferrata Storti Foundation
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3409809/ https://ncbi.nlm.nih.gov/pubmed/22315500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2011.055202 |
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