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Thrombocytosis in children and adolescents—classification, diagnostic approach, and clinical management
Secondary thrombocytosis is a frequent secondary finding in childhood infection and inflammation. Primary hereditary thrombocytosis may be caused by germline mutations within the genes encoding key regulators of thrombopoiesis, i.e., thrombopoietin (THPO) and its receptor c-MPL (MPL) or the receptor...
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| Publicat a: | Ann Hematol |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer Berlin Heidelberg
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8195939/ https://ncbi.nlm.nih.gov/pubmed/33712866 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00277-021-04485-0 |
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