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Stroke and presence of patent foramen ovale in sickle cell disease
Sickle cell disease (SCD) is an inherited monogenic hemoglobinopathy characterized by formation of sickle erythrocytes under conditions of deoxygenation. Sickle erythrocytes can lead to thrombus formation and vaso-occlusive episodes that may result in hemolytic anemia, pain crisis and multiple organ...
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| Publicado no: | J Thromb Thrombolysis |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer US
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7909731/ https://ncbi.nlm.nih.gov/pubmed/33638018 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11239-021-02398-3 |
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