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                             50 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Bayesian Approach to the ICH Q8 Definition of Design Space Peterson, John J.
2008
5 p. 959-975
artikel
2 A Bayesian Design and Analysis for Dose-Response Using Informative Prior Information Smith, Michael K.
2006
5 p. 695-709
artikel
3 A Comparison of False Positive Rates of Peto and Poly-3 Methods for Long-Term Carcinogenicity Data Analysis Using Multiple Comparison Adjustment Method Suggested by Lin and Rahman Rahman, Mohammad A.
2008
5 p. 949-958
artikel
4 Adaptive Dose Selection Using Efficacy-Toxicity Trade-Offs: Illustrations and Practical Considerations Thall, Peter F.
2006
5 p. 623-638
artikel
5 Analysis of Treatment Effectiveness in Longitudinal Observational Data Faries, Douglas
2007
5 p. 809-826
artikel
6 An Estimation Method of the Half-Life for a One-Compartment Model of a Single Bolus Intravenous Injection by a Single Sampling Funatogawa, Takashi
2007
5 p. 827-837
artikel
7 A Permutation Two One-Sided Tests Procedure to Detect Minimal Fold Changes of Gene Expression Levels Liu, Jen-pei
2008
5 p. 808-826
artikel
8 A Predictive Risk Probability Approach for Microarray Data with Survival as an Endpoint Chen, Dung-Tsa
2008
5 p. 841-852
artikel
9 A Procedure for Group Sequential Comparative Poisson Trials Xia, Qi
2007
5 p. 869-881
artikel
10 A Review of: “Assessing Quality of Life in Clinical Trials: Theory and Methods, Second Edition, by P. Fayers and R. Hays (eds.)” Rodenberg, Cynthia A.
2006
5 p. 761-763
artikel
11 A Review of: “Flowgraph Models for Multistate Time-to-Event Data” Commenges, Daniel
2005
5 p. 883-884
artikel
12 A Review of: “Introduction to Randomized Controlled Clinical Trials, Second Edition, by J. N. S. Matthews” Kesler, Karen
2007
5 p. 951-953
artikel
13 A Review of: “Medical Statistics: A Textbook for the Health Sciences, Fourth Edition, by D. Machin, M. J. Campbell, and S. J. Walters” Dhar, Sunil K.
2008
5 p. 1036-1038
artikel
14 A Review of: “Sample Size Calculations in Clinical Research, Second Edition, by S.-C. Chow, J. Shao, and H. Wang” Filloon, Thomas G.
2008
5 p. 1034-1035
artikel
15 A Review of: “Selection Bias and Covariate Imbalances in Randomized Clinical Trials, by V. W. Berger” Friede, Tim
2006
5 p. 757-759
artikel
16 A Review of: “Statistical Analysis of Epidemiologic Data” Hudson, Suzanne
2005
5 p. 885-887
artikel
17 A Review of: “Statistical Evidence in Medical Trials: What Do the Data Really Tell Us?, by S. D. Simon” Dhar, Sunil K.
2007
5 p. 949-950
artikel
18 A Review of: “Statistical Methods for Dose-Finding Experiments, by S. Chevret (Ed.)” Bretz, Frank
2007
5 p. 947-948
artikel
19 A Review of: “The Statistical Analysis of Recurrent Events, by R. J. Cook and J. F. Lawless” Noursalehi, Mojtaba
2008
5 p. 1039-1041
artikel
20 Assessing the Consistency of Traditional Chinese Medicine with Multiple Correlative Active Components Lu, Qingshu
2007
5 p. 791-808
artikel
21 A Two-Stage Binomial Test Approach of Gene Identification in Oligonucleotide Arrays Chen, Dung-Tsa
2007
5 p. 903-918
artikel
22 Bayesian Optimal Designs for a Quantal Dose-Response Study with Potentially Missing Observations Baek, InYoung
2006
5 p. 679-693
artikel
23 Bayesian Optimal Designs for Pharmacokinetic Models: Sensitivity to Uncertainty Dokoumetzidis, Aristides
2007
5 p. 851-867
artikel
24 Block Designs in Method Transfer Experiments Altan, Stan
2008
5 p. 996-1004
artikel
25 Design and Analysis of Analytical Method Transfer Studies Schwenke, James R.
2008
5 p. 1013-1033
artikel
26 Design and Analysis of Dose-Finding Studies Combining Multiple Comparisons and Modeling Procedures Pinheiro, Jose
2006
5 p. 639-656
artikel
27 Equivalence Tests for Shelf Life and Average Drug Content in Stability Studies Djira, Gemechis D.
2008
5 p. 985-995
artikel
28 Estimating a Positive False Discovery Rate for Variable Selection in Pharmacogenetic Studies Li, Lang
2007
5 p. 883-902
artikel
29 Estimation of Lag Time Between Onset of and Death from an Occult Tumor Ahn, Hongshik
2008
5 p. 901-914
artikel
30 Fallback Tests in Dose-Response Clinical Trials Dmitrienko, Alex
2006
5 p. 745-755
artikel
31 Guest Editors' Note for the Special Issue on “Design and Analysis of Dose-Response Clinical Trials” Ting, Naitee
2006
5 p. 1-2
artikel
32 Hypothesis Testing and Bayesian Estimation using a Sigmoid Emax Model Applied to Sparse Dose-Response Designs Thomas, Neal
2006
5 p. 657-677
artikel
33 Identifying High-Dimensional Biomarkers for Personalized Medicine via Variable Importance Ranking Baek, Songjoon
2008
5 p. 853-868
artikel
34 Incremental Forward Feature Selection with Application to Microarray Gene Expression Data Lee, Yuh-Jye
2008
5 p. 827-840
artikel
35 Innovative Approaches in Drug Development Chang, Mark
2007
5 p. 775-789
artikel
36 Mixture Model Framework Facilitates Understanding of Zero-Inflated and Hurdle Models for Count Data Baughman, A. L.
2007
5 p. 943-946
artikel
37 Multiple Comparisons and Multiple Contrasts in Randomized Dose-Response Trials—Confidence Interval Oriented Approaches Hothorn, Ludwig A.
2006
5 p. 711-731
artikel
38 Multispectra CWT-Based Algorithm (MCWT) in Mass Spectra for Peak Extraction Hsueh, Huey-Miin
2008
5 p. 869-882
artikel
39 Overall Type I Error Rate and Power of Multiple Dunnett's Tests on Rodent Body Weights in Toxicology Studies Hoffman, Wherly P.
2008
5 p. 883-900
artikel
40 Parametric Two-Tier Sequential Quality Assurance Test of Delivery Dose Uniformity of Multiple-Dose Inhaler and Dry Powder Inhaler Drug Products Tsong, Yi
2008
5 p. 976-984
artikel
41 Phase I Studies of Chemotherapeutic Agents in Cancer Patients: A Review of the Designs Potter, Douglas M.
2006
5 p. 579-604
artikel
42 Poly-k-Trend Tests for Survival Adjusted Analysis of Tumor Rates Formulated as Approximate Multiple Contrast Test Schaarschmidt, Frank
2008
5 p. 934-948
artikel
43 Population Pharmacokinetic Measures, Their Estimation and Selection of Sampling Times Fedorov, Valerii
2007
5 p. 919-941
artikel
44 Proof of Hazard and Proof of Safety in Toxicological Studies Using Simultaneous Confidence Intervals for Differences and Ratios to Control Hothorn, Ludwig A.
2008
5 p. 915-933
artikel
45 Sample Size Calculation for Weighted Rank Tests Comparing Survival Distributions Under Cluster Randomization: A Simulation Method Jung, Sin-Ho
2007
5 p. 839-849
artikel
46 Sequential Designs for Logistic Phase I Clinical Trials Liu, Guohui
2006
5 p. 605-621
artikel
47 Special Issue on Non-Clinical Statistics Guest Editors' Notes Chen, James J.
2008
5 p. 805-807
artikel
48 Statistical Assessment of Analytical Method Transfer Zhong, Jinglin
2008
5 p. 1005-1012
artikel
49 Subgroup Analyses in Randomized Clinical Trials: Statistical and Regulatory Issues Grouin, Jean-Marie
2005
5 p. 869-882
artikel
50 Using the Partitioning Principle to Adaptively Design Dose-Response Studies Ling, Xiang
2006
5 p. 733-743
artikel
                             50 gevonden resultaten
 
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