Advances in the clinical management of high‐risk Wilms tumors
Outcomes are excellent for the majority of patients with Wilms tumors (WT). However, there remain WT subgroups for which the survival rate is approximately 50% or lower. Acknowledging that the composition of this high‐risk group has changed over time reflecting improvements in therapy, we introduce...
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Veröffentlicht in: | Pediatric blood & cancer 2023-03, Vol.70 (3), p.e30153-n/a |
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Sprache: | eng |
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