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Systemic therapy in pediatric-type soft-tissue sarcoma
Soft-tissue sarcoma (sts) is rare and represents approximately 7% of cancers in children and in adolescents less than 20 years of age. Rhabdomyosarcoma (rms) is most prevalent in children less than 10 years of age and peaks again during adolescence (16–19 years of age). Multi-agent chemotherapy cons...
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| Publicat a: | Curr Oncol |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Multimed Inc.
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7050042/ https://ncbi.nlm.nih.gov/pubmed/32174753 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3747/co.27.5481 |
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