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Statistics in Medicine|May 11, 2006
Planning and analysis of three-arm non-inferiority trials with binary endpointsMeinhard Kieser, Tim FriedeStatistics in Medicine|April 6, 2006
A method for therapeutic dose selection in a phase II clinical trial using contrast statisticsAkira Wakana, Isao Yoshimura, Chikuma HamadaStatistics in Medicine|April 28, 2006
An introductory note to CHMP guidelines: choice of the non-inferiority margin and data monitoring committeesDavid Brown, Peter Volkers, Simon DayStatistics in Medicine|April 15, 2004
Eight interval estimators of a common rate ratio under stratified Poisson samplingKung-Jong LuiStatistics in Medicine|June 15, 1992
Comparisons between a new drug and active and placebo controls in an efficacy clinical trialC W Dunnett, A C TamhaneStatistics in Medicine|June 15, 1992
A method of designing clinical trials for combination drugsJ G Pigeon, M D Copenhaver, J P WhippleStatistics in Medicine|June 15, 1992
Comparing sample size formulae for trials with unbalanced allocation using the logrank testF Y HsiehStatistics in Medicine|June 15, 1992
Sample sizes for proportional hazards survival studies with arbitrary patient entry and loss to follow-up distributionsN A Yateman, A M SkeneStatistics in Medicine|September 28, 2004
Dependency issues in survival analyses of 55,782 primary hip replacements from 47,355 patientsStein Atle Lie, Lars B Engesaeter, Leif I Havelin, et al.Statistics in Medicine|June 28, 2005
Individual growth curve models for assessing evidence-based referral criteria in growth monitoringP van Dommelen, S van Buuren, G R J Zandwijken, et al.Pageof 1,054