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Hemoglobin Sickle Cell Disease and Systemic Lupus Erythematosus
An unusual association of hemoglobin sickle cell disease with systemic lupus erythematosus in an 11-year-old girl highlights the diagnostic dilemma that may arise because of the similarity of symptomatology.
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
1984
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2561782/ https://ncbi.nlm.nih.gov/pubmed/6502719 |
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