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Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease
Thrombocytosis is common in sickle cell disease and may contribute to vaso‐occlusion. Hydroxyurea treats extreme thrombocytosis. Acquired von Willebrand disease should be considered prior to aspirin therapy.
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| Gepubliceerd in: | Clin Case Rep |
|---|---|
| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
John Wiley and Sons Inc.
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7813102/ https://ncbi.nlm.nih.gov/pubmed/33489197 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.3556 |
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