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Dyserythropoiesis and myelodysplasia in thiamine‐responsive megaloblastic anemia syndrome
The case of thiamine‐responsive megaloblastic anemia (TRMA) presented here speculates the need early diagnosis, continuous monitoring, follow‐up, and regulated treatment plan for the patients. Complications and systemic manifestations are likely to enhance in otherwise circumstances.
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| Publicado no: | Clin Case Rep |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7303871/ https://ncbi.nlm.nih.gov/pubmed/32577249 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.2791 |
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