Using time-to-event analysis methodology requires careful definition of the event, censored observation, provision of adequate follow-up, number of events, and independence or ‘noninformativeness’ of the censoring mechanisms relative to the event. Design and Analysis of Clinical Trials with Time-to-Event Endpoints provides a thorough presentation o
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格式 PDF ● 网页 616 ● ISBN 9781420066401 ● 编辑 Karl E. (Georgia Southern University, USA) Peace ● 出版者 CRC Press ● 发布时间 2009 ● 下载 3 时 ● 货币 EUR ● ID 4116120 ● 复制保护 Adobe DRM
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