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Adverse Events Following Infusion of T Cells for Adoptive Immunotherapy: A 10 Year Experience
BACKGROUND: The FDA currently recommends at least 4 hours of recipient monitoring to detect early infusion reactions; recent catastrophic reactions to “first in man” biological agents have emphasized the importance of this rule for initial studies of new products. The value of such monitoring for be...
Gorde:
| Egile Nagusiak: | , , , , , , , , , , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2010
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2914831/ https://ncbi.nlm.nih.gov/pubmed/20429793 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/14653241003709686 |
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