Works matching IS 15391604 AND DT 2011 AND VI 10 AND IP 4
Results: 18
Literature Review January-March 2011.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 379, doi. 10.1002/pst.495
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Evaluating surrogate variables for improving microarray multiple testing inference.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 302, doi. 10.1002/pst.466
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A guide to the design and analysis of small clinical studies.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 363, doi. 10.1002/pst.477
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An adaptive seamless phase II/III design for oncology trials with subpopulation selection using correlated survival endpoints.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 347, doi. 10.1002/pst.472
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Mixed models for data from thorough QT studies: Part 2. One-step assessment of conditional QT prolongation.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 293, doi. 10.1002/pst.465
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Sample size re-estimation for survival data in clinical trials with an adaptive design.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 325, doi. 10.1002/pst.469
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Review of JMP genomics.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 384, doi. 10.1002/pst.460
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Block response-adaptive randomization in clinical trials with binary endpoints.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 341, doi. 10.1002/pst.471
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Validating clinical trial data reporting with SAS, Matthews CI, Shilling BC (2008) ISBN: 9781599941288; 228 pages; $36.95, £52.05 SAS Institute Inc.;.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 383, doi. 10.1002/pst.424
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A ratio-to-control Williams-type test for trend.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 289, doi. 10.1002/pst.464
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Testing non-inferiority and superiority for two endpoints for several treatments with a control.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 318, doi. 10.1002/pst.468
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Assessing non-inferiority to an aggregate response with an application to development of pneumococcal conjugate vaccines.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 332, doi. 10.1002/pst.470
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Assessing departure from dose linearity under a repeated measures incomplete block design.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 357, doi. 10.1002/pst.474
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Six sigma in the pharmaceutical industry Brian K Nunnally, and John S McConnell (2007) ISBN: 1420054392; 224 pages; £59.99, €48.90, $93.95 Chapman & Hall/CRC;.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 381, doi. 10.1002/pst.405
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- Article
The perils with the misuse of predictive power.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 311, doi. 10.1002/pst.467
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A flexible multi-stage design for phase II oncology trials.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 369, doi. 10.1002/pst.478
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Pharmaceutical Statistics Using SAS<sup>®</sup>: A Practical Guide Alex Dmitrienko, Christy Chuang-Stein, Ralph D'Agostino ISBN: 978-1-59047-886-8, 444 pages; $69.95, £98.54; SAS Institute Inc;.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 382, doi. 10.1002/pst.411
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- Article
A note on dealing with missing standard errors in meta-analyses of continuous outcome measures in WinBUGS.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 374, doi. 10.1002/pst.491
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