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Robust inference in discrete hazard models for randomized clinical trials
Time-to-event data in which failures are only assessed at discrete time points are common in many clinical trials. Examples include oncology studies where events are observed through periodic screenings such as radiographic scans. When the survival endpoint is acknowledged to be discrete, common met...
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Päätekijät: | , |
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Aineistotyyppi: | Artigo |
Kieli: | Inglês |
Julkaistu: |
2012
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Aiheet: | |
Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3440522/ https://ncbi.nlm.nih.gov/pubmed/22810273 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10985-012-9224-6 |
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