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A phase I trial of two sequence-specific schedules of decitabine and vorinostat in patients with acute myeloid leukemia
This phase I trial evaluated two schedules of escalating vorinostat in combination with decitabine every 28 days: (i) sequential or (ii) concurrent. There were three dose-limiting toxicities: grade 3 fatigue and generalized muscle weakness on the sequential schedule (n = 1) and grade 3 fatigue on th...
Αποθηκεύτηκε σε:
Τόπος έκδοσης: | Leuk Lymphoma |
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Κύριοι συγγραφείς: | , , , , , , , , , , , , , , , , , , , , |
Μορφή: | Artigo |
Γλώσσα: | Inglês |
Έκδοση: |
2015
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Θέματα: | |
Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4688006/ https://ncbi.nlm.nih.gov/pubmed/25682963 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/10428194.2015.1018248 |
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