Digitale Bibliotheek
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                             243 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 68 A bayesian approach to modeling the relation between treatment benefit and underlying risk in meta-analysis Sharp, Stephen
1997
18 3S1 p. S83-
1 p.
artikel
2 81 A data management system allowing multi-institutional clinical trials to deliver secure communications and Good Clinical Laboratory Practice Standards on the World-Wide Web Schuette, R.Wade
1997
18 3S1 p. S91-
1 p.
artikel
3 87 A data warehousing approach to support clinical trials research Niland, Joyce C.
1997
18 3S1 p. S95-
1 p.
artikel
4 77 Adjusting survival analysis for the presence of nonadjudicated potential study events Cook, Thomas
1997
18 3S1 p. S89-
1 p.
artikel
5 08 A global measure of influence for the Cox regression model Barlow, William E.
1997
18 3S1 p. S45-S46
2 p.
artikel
6 34 A mixture model for the chance to conceive in subfertile couples based on the beta-distribution Eijkemans, M.J.C.
1997
18 3S1 p. S61-S62
2 p.
artikel
7 98 Analysis of data from longitudinal clinical trials with drop-outs Jansson, Gary
1997
18 3S1 p. S102-S103
2 p.
artikel
8 89 An automatic coding system Maupas, Jean
1997
18 3S1 p. S96-
1 p.
artikel
9 29 A new bayesian design for phase I cancer clinical trials Toledano, Alicia Y.
1997
18 3S1 p. S58-
1 p.
artikel
10 62 A new randomization method for allocating subjects Chappell, Rick
1997
18 3S1 p. S79-S80
2 p.
artikel
11 84 An innovative approach to clinical trial conduction using internet DeRosa, M.
1997
18 3S1 p. S93-
1 p.
artikel
12 52 Application of gee procedures for sample size calculations in repeated measures experiments Rochon, James
1997
18 3S1 p. S73-
1 p.
artikel
13 11 Approaches to using predicted values in randomized Clinical Trials Goedhart, Dick
1997
18 3S1 p. S47-S48
2 p.
artikel
14 24 A proportional odds random effects model for repeated ordered responses Santos, Dirley Moreira Dos
1997
18 3S1 p. S55-
1 p.
artikel
15 17 A review and assessment of the participant recruitment strategies employed in the NSABP Breast Cancer Prevention Trial Cronin, Walter M.
1997
18 3S1 p. S51-
1 p.
artikel
16 109 A sequential design for studies with repeated measures on multiple outcomes Leroux, Brian G.
1997
18 3S1 p. S109-
1 p.
artikel
17 110 A three-armed equivalence study Lange, S.
1997
18 3S1 p. S109-S110
2 p.
artikel
18 13 A unified family of group sequential designs Emerson, Scott S.
1997
18 3S1 p. S49-
1 p.
artikel
19 Author Index 1997
18 3S1 p. S191-S211
21 p.
artikel
20 26 Bayesian decision procedures for phase I dose-escalation studies Whitehead, John
1997
18 3S1 p. S56-
1 p.
artikel
21 32 Building multivariable prognostic models: Transformation of the predictors using fractional polynomials Sauerbrei, Willi
1997
18 3S1 p. S60-
1 p.
artikel
22 Calender of program 1997
18 3S1 p. S4-S39
36 p.
artikel
23 49 Case-control design using multivariate generalization of the cox model: Application to central catheters related bacteremia Mahe, Cédric
1997
18 3S1 p. S71-
1 p.
artikel
24 18 Challenges faced in recruiting patients from primary care practices into a behavioral modification trial Margitić, Susan
1997
18 3S1 p. S52-
1 p.
artikel
25 74 Challenges of adverse experience reporting, coding and analysis: areas for improvement Krause-Steinrauf, Heidi
1997
18 3S1 p. S87-S88
2 p.
artikel
26 41 Challenges of the prevention of events with angiotensin converting enzyme inhibition trial 1997
18 3S1 p. S66-
1 p.
artikel
27 55 Changes in sample size and length of follow-up to maintain power in the cabg patch trial Bigger, J.T.
1997
18 3S1 p. S75-
1 p.
artikel
28 70 Choosing an appropriate dichotomous effect measure for meta-analysis: Empirical evidence of the appropriateness of the odds ratio and relative risk Deeks, J.J.
1997
18 3S1 p. S84-S85
2 p.
artikel
29 14 Clinical equivalence test and confidence interval for the difference in proportions for the paired-sample design Tango, Toshiro
1997
18 3S1 p. S49-S50
2 p.
artikel
30 23 Clinically relevant analyses of diary card data in asthma studies Mander, Adrian
1997
18 3S1 p. S55-
1 p.
artikel
31 42 Clinical monitoring of children's development in the dietary intervention study in children Barton, Bruce
1997
18 3S1 p. S66-S67
2 p.
artikel
32 63 Clinical trials with dichotomous endpoints: Should we correct for baseline characteristics? Steyerberg, E.W.
1997
18 3S1 p. S80-
1 p.
artikel
33 30 Comparison of competing parametric survival models — a bayesian perspective Abrams, Keith R.
1997
18 3S1 p. S59-
1 p.
artikel
34 43 Comparison of routine and survey data for the evaluation of a community randomized trial: A case study Sterne, J.A.C.
1997
18 3S1 p. S67-
1 p.
artikel
35 88 Computerized intervention tracking system for data management and protocol adherence Hogan, Patricia
1997
18 3S1 p. S95-S96
2 p.
artikel
36 108 Conditional power for weighted log-rank statistics with covariate adjustments Yao, Qing
1997
18 3S1 p. S108-S109
2 p.
artikel
37 78 Controlling survival comparisons to reflect subgroup analyses in phase III clinical trials Bryant, John
1997
18 3S1 p. S90-
1 p.
artikel
38 104 Design of the economic evaluation of the sortie trial Mauldin, Patrick D.
1997
18 3S1 p. S106-
1 p.
artikel
39 91 Design of the randomized evaluation of strategies for left ventricular dysfunction (resolvd) pilot study: A trial of combination neurohormonal blockade in patients with congestive heart failure Tsuyuki, Ross T.
1997
18 3S1 p. S98-
1 p.
artikel
40 10 Development of a clinical prediction model for an ordinal diagnostic outcome Harrell Jr., Frank E.
1997
18 3S1 p. S47-
1 p.
artikel
41 106 Early termination of a clinical trial when there is evidence that the treatment will ultimately not prove beneficial: protocol b-14 of the national surgical adjuvant breast and bowel project Dignam, James
1997
18 3S1 p. S107-S108
2 p.
artikel
42 71 EFfects of double data entry vs. single data entry as employed during a large multicenter perinatal clinical trial Weston, Julie
1997
18 3S1 p. S85-
1 p.
artikel
43 28 Empirical bayes methods in the annual quality comparison and ranking of dutch gynecological centres Brand, Ronald
1997
18 3S1 p. S57-S58
2 p.
artikel
44 16 Enrollment of women of childbearing potential in a NIH-sponsored clinical trial Mickel, Mary
1997
18 3S1 p. S51-
1 p.
artikel
45 25 Estimating the parameters of a random effects logistic model with the Nonparametric Maximum Likelihood Method (NPML) Mesnil, Florence
1997
18 3S1 p. S56-
1 p.
artikel
46 56 Ethics and practice: Alternative designs for phase III Randomized clinical trials Rosenberger, William V.
1997
18 3S1 p. S76-
1 p.
artikel
47 96 Evaluation of predictors and impact of losses to follow-up in the domain of hiv infection Ioannidis, John P.A.
1997
18 3S1 p. S101-S102
2 p.
artikel
48 105 Evaluation of responsiveness of health scales for outcome measurement in clinical trials Holle, Rolf
1997
18 3S1 p. S107-
1 p.
artikel
49 94 Evaluation of standard treatment strategies in a large, multicenter trial: Design issues Rosenberg, Yves
1997
18 3S1 p. S100-
1 p.
artikel
50 60 Experiences of a biostatistician on a research ethics committee Vail, Andy
1997
18 3S1 p. S78-
1 p.
artikel
51 66 Explaining heterogeneity in meta-analysis: A comparison of methods Thompson, Simon G.
1997
18 3S1 p. S82-
1 p.
artikel
52 72 Factors that affect timely submission of forms to a data management center Lancaster, Scott
1997
18 3S1 p. S86-
1 p.
artikel
53 107 Global monitoring of prevention trials: the breast cancer prevention trial (bcpt) experience Anderson, Stewart J.
1997
18 3S1 p. S108-
1 p.
artikel
54 64 Global tests for multiple endpoints in clinical trials McDermott, Michael P.
1997
18 3S1 p. S81-
1 p.
artikel
55 100 Group comparisons involving missing data in clinical trials: use of observed versus imputed data Miller, Michael E.
1997
18 3S1 p. S103-S104
2 p.
artikel
56 58 How informed is ‘informed’ consent? Participants' responses to random allocation of critically ill neonates to alternative treatments in the UK collaboration ECMO trial Elbourne, D.
1997
18 3S1 p. S77-
1 p.
artikel
57 35 How to perform the two-stage analysis of cross-over trials if you can't be persuaded not to Senn, Stephen
1997
18 3S1 p. S62-
1 p.
artikel
58 44 Identification of strategies to ensure patients continue taking study medication — results from the lipid study 1997
18 3S1 p. S68-
1 p.
artikel
59 20 Implementing a centralized protocol-patient accrual system — short and long term benefits Van-Tull, Bonita
1997
18 3S1 p. S53-
1 p.
artikel
60 69 Inclusion of both patient level and study-level covariates in a meta-analysis Higgins, Julian P.T.
1997
18 3S1 p. S84-
1 p.
artikel
61 101 Incorporating a quality of life assessment into an ongoing multi-center clinical trial: problems and recommendations 1997
18 3S1 p. S104-
1 p.
artikel
62 86 In-house code generators: A rad new concept Terrell, J.Timothy
1997
18 3S1 p. S94-
1 p.
artikel
63 82 Internet security in clinical trial data management systems Martin, Jeffrey P.
1997
18 3S1 p. S92-
1 p.
artikel
64 95 Issues in running a sequential randomized trial in pressure sore prevention Brown, Julia
1997
18 3S1 p. S101-
1 p.
artikel
65 93 Issues in the design of a multicenter trial comparing radiation therapy to expandable esophageal stents for patients with advanced unresectable esophageal cancer Redmond, Carol K.
1997
18 3S1 p. S99-S100
2 p.
artikel
66 97 Late visit reports to ensure patient retention Zadnik, Karla
1997
18 3S1 p. S102-
1 p.
artikel
67 Letter from the president 1997
18 3S1 p. S1-
1 p.
artikel
68 79 Link-based models for survival data with random interval and continuous time censoring Younes, Naji
1997
18 3S1 p. S90-S91
2 p.
artikel
69 05 Local data management in cancer clinical trials Haining, Shona A.
1997
18 3S1 p. S43-S44
2 p.
artikel
70 46 Logistic regression upon a continuous covariate with a changepoint Signorini, David F.
1997
18 3S1 p. S69-
1 p.
artikel
71 22 Longitudinal analysis of sinusoidality of time-qualified data Shyr, Yu
1997
18 3S1 p. S54-
1 p.
artikel
72 67 Measures of heterogeneity in meta-analysis Seagroatt, Valerie
1997
18 3S1 p. S82-S83
2 p.
artikel
73 04 Measuring workload of cancer clinical trials: A multi-centre study by the clinical research associates (CRA) committee of the national cancer institute of Canada clinical trials group (NCIC CTG) Roche, Kathryn
1997
18 3S1 p. S43-
1 p.
artikel
74 76 Modeling survival data with multiple ordinal outcomes Berridge, Damon Mark
1997
18 3S1 p. S89-
1 p.
artikel
75 07 On the choice of regression model for censored Survival data Stare, Janez
1997
18 3S1 p. S45-
1 p.
artikel
76 31 Optimal design in nonlinear regression random effects models — application in population pharmacokinetics Mentré, France
1997
18 3S1 p. S59-S60
2 p.
artikel
77 15 Optimization of testing times and critical values in sequential equivalence testing Müller, Hans-Helge
1997
18 3S1 p. S50-
1 p.
artikel
78 33 Overfit in logistic regression Schemper, Michael
1997
18 3S1 p. S61-
1 p.
artikel
79 P97 Accidental exposure of central laboratory personnel to potentially infectious clinical trial specimens. What are the issues? Wasilauskas, Carol H.
1997
18 3S1 p. S171-
1 p.
artikel
80 P91 A comparison of sample size methods for survival studies Benner, Axel
1997
18 3S1 p. S167-
1 p.
artikel
81 P65 A data management system for assessing health outcomes in an inner city managed care asthma patient population Levenson, Suzette M.
1997
18 3S1 p. S150-
1 p.
artikel
82 P05 Adequacy of the proportional hazards model using lin, wei and ying plots O'Quigley, John
1997
18 3S1 p. S113-
1 p.
artikel
83 P49 Age at any birth and breast cancer risk Robertson, Chris
1997
18 3S1 p. S140-
1 p.
artikel
84 P121 Aggregate patient data meta-analyses with time-to-event endpoints: An example from surgery Williamson, Paula
1997
18 3S1 p. S184-S185
2 p.
artikel
85 P88 A multi-state markov process model for quality of life and survival in large heart failure clinical trials Charlesworth, A.
1997
18 3S1 p. S165-
1 p.
artikel
86 P68 An alternative to the customary reporting of common toxicity criteria Anderson, Stewart
1997
18 3S1 p. S152-
1 p.
artikel
87 P106 Analysis of ordered categorical data: Towards a stratified model Savaluny, Elly
1997
18 3S1 p. S176-
1 p.
artikel
88 P47 Analysis of risk factors for adverse drug reaction in pharmaco-epidemiologic case control studies Schäfer, Helmut
1997
18 3S1 p. S139-
1 p.
artikel
89 P104 Analysis of the titration procedure for warfarin in the post coronary artery bypass graft (POST CABG) clinical trial Canner, Joseph
1997
18 3S1 p. S175-
1 p.
artikel
90 P31 analyzing chemosensitivity assays for Acute Myelogenic Leukemia Simpson, P.M.
1997
18 3S1 p. S129-
1 p.
artikel
91 P52 Analyzing compliance in clinical trials: A sensitive point Goetghebeur, Els
1997
18 3S1 p. S142-
1 p.
artikel
92 P06 Analyzing the structure of the hazard function Mocks, Joachim
1997
18 3S1 p. S114-
1 p.
artikel
93 P61 An automated clinical center payment system Corky, Scott
1997
18 3S1 p. S147-
1 p.
artikel
94 P02 An investigation of the effect of covariate adjustment in a sequential clinical trial Sahdra, M.
1997
18 3S1 p. S111-S112
2 p.
artikel
95 P64 An optimal network access in a patient registration system Nibhanupudi, Mohan
1997
18 3S1 p. S149-
1 p.
artikel
96 P99 Application of “design”s functions to build multivariate models for predicting coronary artery disease 1997
18 3S1 p. S172-
1 p.
artikel
97 P24 a quality assurance monitoring system: The national cancer institute clinical cooperative oncology group experience Smith, Gary
1997
18 3S1 p. S125-
1 p.
artikel
98 P32 a quality control analysis to be used in determining whether or not the enzyme-linked immunosorbent assay is in control Johnson, Paul
1997
18 3S1 p. S130-
1 p.
artikel
99 P15 A quantitative protocol evaluation system Herson, Jay
1997
18 3S1 p. S119-
1 p.
artikel
100 P125 Are patients in a clinical trial representative? Stead, Maxine
1997
18 3S1 p. S187-
1 p.
artikel
101 P46 Assessing the effects of treatment in observational studies: Adjusting for disease severity Sabin, Caroline A.
1997
18 3S1 p. S138-S139
2 p.
artikel
102 P40 Assessing the risk of severe infectious disease when immunosuppressive drugs are administered during the study period Heinzl, Harald
1997
18 3S1 p. S134-S135
2 p.
artikel
103 P22 assessment of data quality in an nihsponsored multicenter clinical trial: The hemodialysis (HEMO) study 1997
18 3S1 p. S123-S124
2 p.
artikel
104 P53 Capture-recapture with two sources: Controlling for covariates Tilling, K.
1997
18 3S1 p. S142-S143
2 p.
artikel
105 P75 Challenges in implementing a telephone touch-tone randomization system in the primary care setting Anthony, Susan
1997
18 3S1 p. S156-S157
2 p.
artikel
106 P83 Cohort maintenance in the NHLBI growth and health study (NGHS) Similo, Shari
1997
18 3S1 p. S161-S162
2 p.
artikel
107 P116 Comparing statistical methods in meta-analyzing pooled data sets Scheuchenpflug, Thomas
1997
18 3S1 p. S181-S182
2 p.
artikel
108 P108 Comparing structures among groups by latent class analysis: An application of cognitive impairment scale Lin, Ting Hsiang
1997
18 3S1 p. S177-S178
2 p.
artikel
109 P39 Comparing two approaches for analyzing data with clumping at zero Chang, Bei-Hung
1997
18 3S1 p. S134-
1 p.
artikel
110 P130 Comparison between univariate and multivariate prognostic index to evaluate treatment efficacy in subgroups of patient at different risks of death. Data from a systematic overview Santoro, Luigi
1997
18 3S1 p. S190-
1 p.
artikel
111 P17 Comparison of medical record review with prospective data collection in randomized trials Rajab, Mohammad H.
1997
18 3S1 p. S120-
1 p.
artikel
112 P19 Comparison of participants and non-participants in a clinical trial of funguria 1997
18 3S1 p. S121-
1 p.
artikel
113 P73 Comparison of the accuracy of centralized double key data entry and single key interactive data entry Ellis, Nancy
1997
18 3S1 p. S155-
1 p.
artikel
114 P79 Compliance with qol assessment in a multicentre international breast cancer trial Olschewski, Manfred
1997
18 3S1 p. S159-
1 p.
artikel
115 P42 Components of chance-corrected agreement in the assessment of gastritis: Practical implications Tinelli, Carmine
1997
18 3S1 p. S136-
1 p.
artikel
116 P82 Confidence intervals for cost-effectiveness ratios: The use of bootstrapping Campbell, Marion K.
1997
18 3S1 p. S161-
1 p.
artikel
117 P29 Considering the patient's quality of life in a bayesian clinical trial design Ballas, Dália
1997
18 3S1 p. S128-
1 p.
artikel
118 P119 Construction of height and weight growth charts for iran from hierarchically structured data; With an investigation of appropriate statistical methods Hosseini, Mostafa
1997
18 3S1 p. S183-S184
2 p.
artikel
119 P123 Contradictory results from consecutive clinical trials: A cautious approach to explanations 1997
18 3S1 p. S186-
1 p.
artikel
120 P54 Controversial role of age as a prognostic factor in multiple myeloma Klersy, Catherine
1997
18 3S1 p. S143-
1 p.
artikel
121 P67 Data form entry using internet tools: The matrix system Echement, Deborah A.
1997
18 3S1 p. S151-
1 p.
artikel
122 P70 Data management and analytic support for an international individual patient data meta-analysis (IPD-MA) Owen, Walter
1997
18 3S1 p. S153-
1 p.
artikel
123 P71 Data management aspects of a systematic overview of individual data from 100,000 patients in randomized trials Santoro, Eugenio
1997
18 3S1 p. S154-
1 p.
artikel
124 P74 Data operations management with clinical datafax: The prostate cancer prevention trial (PCPT) experience Ryan, Anne M.
1997
18 3S1 p. S156-
1 p.
artikel
125 P21 data quality monitoring in a collaborative multi-center study: the interstitial cystitis data base (ICDB) study Matthews, Yvonne L.
1997
18 3S1 p. S123-
1 p.
artikel
126 P59 Design and implementation of a clinical research database in client/server architecture Wu, Daniel
1997
18 3S1 p. S146-
1 p.
artikel
127 P04 Detecting outliers by the grand tour Bartkowiak, Anna
1997
18 3S1 p. S113-
1 p.
artikel
128 P114 Development of a protocol office: A concept for the 1990's Flaherty, Sandra
1997
18 3S1 p. S180-S181
2 p.
artikel
129 P07 Effect of a non-susceptible fraction on standard survival analysis methods Schnell, Daniel J.
1997
18 3S1 p. S114-
1 p.
artikel
130 P57 Electronic systems for handling adverse event reports Wong, Kenneth
1997
18 3S1 p. S145-
1 p.
artikel
131 73 Pen-based remote data entry system in a multicenter clinical trial Salvi, Junca
1997
18 3S1 p. S86-S87
2 p.
artikel
132 P94 Establishing a system for prospective registration of human subjects participating in research studies at a comprehensive cancer center Houston, Collette
1997
18 3S1 p. S169-
1 p.
artikel
133 P93 Establishing the ethics of randomization in breast cancer trials Abrams, Keith R.
1997
18 3S1 p. S168-S169
2 p.
artikel
134 P01 Estimation in group sequential designs using simulated estimating equations LeBlanc, Michael
1997
18 3S1 p. S111-
1 p.
artikel
135 P11 Evaluation of a two-phase enrollment design: Experience of the age-related eye disease study (AREDS) 1997
18 3S1 p. S116-S117
2 p.
artikel
136 P09 Evaluation of the bias in using the time to the ferst event in the analysis of clinical trials of atrial fibrillation Rose, M.S.
1997
18 3S1 p. S115-
1 p.
artikel
137 P03 Graphical presentation of clinical trials results Spino, Cathie
1997
18 3S1 p. S112-
1 p.
artikel
138 P72 Hands on user training following a clinical research database upgrade Marks, Linda D.
1997
18 3S1 p. S154-S155
2 p.
artikel
139 P20 Huge variability in data quality exists according to country Tardiff, Barbara E.
1997
18 3S1 p. S122-
1 p.
artikel
140 P95 Human subjects review in long-term prevention trials: Recommendations from the caret experience Boyle, M.Margaret
1997
18 3S1 p. S170-
1 p.
artikel
141 P112 Identification of neonatal hearing impairment: Study design Fletcher, Kristin A.
1997
18 3S1 p. S179-S180
2 p.
artikel
142 P13 Identifying the effect of the learning curve in clinical trials Ramsay, Craig
1997
18 3S1 p. S118-
1 p.
artikel
143 P80 Identifying the types of missingness in longitudinal quality of life data from clinical trials Bacchi, Marisa
1997
18 3S1 p. S159-S160
2 p.
artikel
144 45 Pill counting and attainment of blood pressure goals in the african american study of kidney disease and hypertension (AASK) Greene, Paul
1997
18 3S1 p. S68-S69
2 p.
artikel
145 P96 Impact of equipoise, treatment presentation and severity of disease on informed consent to a randomized clinical trial a randomized trial in health subjects Gallo, C.
1997
18 3S1 p. S170-S171
2 p.
artikel
146 P92 Impact of fixed and stochastic selection at entry on regression to the mean and study power: Application to recurrent events McMahon, Robert P.
1997
18 3S1 p. S168-
1 p.
artikel
147 P77 Impact of trials with null number of events in meta-analysis Cucherat, Michel
1997
18 3S1 p. S158-
1 p.
artikel
148 P69 Improving compliance — the administration of quality of life questionnaires within cancer clinical trials Poulter, Karen
1997
18 3S1 p. S152-S153
2 p.
artikel
149 P126 Including literature data in individual patient data meta-analyses for time-to-event endpoints Collette, Laurence
1997
18 3S1 p. S188-
1 p.
artikel
150 P100 Individualizing patient therapy Senn, Stephen
1997
18 3S1 p. S173-
1 p.
artikel
151 P120 Individual patient data meta-analyses for time-to-event outcomes: An example from epilepsy Williamson, Paula
1997
18 3S1 p. S184-
1 p.
artikel
152 P105 Insight in analgesic trials through pharmacokinetic/pharmacodynamic analysis and simulation Mandema, Jaap W.
1997
18 3S1 p. S175-S176
2 p.
artikel
153 P38 intention-to-treat and vaccine efficacy trials Horne, Amelia Dale
1997
18 3S1 p. S133-
1 p.
artikel
154 P51 Interaction of epidemic and individual heterogeneity on target populations of clinical trials Ioannidis, John A.
1997
18 3S1 p. S141-
1 p.
artikel
155 P18 Interest of cardiac natriuretic peptides for risk stratification in heart failure trials Ahn, Syvlie
1997
18 3S1 p. S120-S121
2 p.
artikel
156 P127 Inter-reviewer variation the validata experience Strang, W.N.
1997
18 3S1 p. S188-S189
2 p.
artikel
157 P113 Investigator-initiated clinical trials: What academicians need to know Herr, Barbara E.
1997
18 3S1 p. S180-
1 p.
artikel
158 P66 Is central adjudication necessary to avoid bias in clinical outcomes? Pogue, Janice
1997
18 3S1 p. S150-S151
2 p.
artikel
159 P101 Longitudinal binary data analysis of use of contraceptive barrier methods Wong, Emelita
1997
18 3S1 p. S173-
1 p.
artikel
160 P27 longitudinal modeling of medical research data with a bayesian belief network Clarke, Ellis J.
1997
18 3S1 p. S126-S127
2 p.
artikel
161 P89 Measurement of sociodemographic characteristics in chronic disorder populations and their relationship to quality of life Sereika, S.
1997
18 3S1 p. S166-
1 p.
artikel
162 P08 Numbers of events needed in comparing survival data to a standard population using the subjects-years method Tu, Dongsheng
1997
18 3S1 p. S115-
1 p.
artikel
163 09 Poisson regression direct adjustment comparison of lifetables Lachin, John M.
1997
18 3S1 p. S46-
1 p.
artikel
164 P28 optimal phase II trial size from decision theory Hart, Augustinus A.M.
1997
18 3S1 p. S127-
1 p.
artikel
165 P16 Optimizing the composing of weight-adjusted drug doses from preselected stock sizes Kaplan, Howard L.
1997
18 3S1 p. S119-
1 p.
artikel
166 53 Power comparisons among different number of categories under ordered polytomous logistic regression model Jeong, Jong-Hyeon
1997
18 3S1 p. S74-
1 p.
artikel
167 P25 Peace automated randomization and drug assignment system 1997
18 3S1 p. S125-S126
2 p.
artikel
168 P62 Pen-computer assisted personal interviewing in a follow-up study of cognitive disorders in an institutionalized elderly population Junca, S.
1997
18 3S1 p. S148-
1 p.
artikel
169 P60 Problems and solutions in running a large multi-centre, community-based study 1997
18 3S1 p. S147-
1 p.
artikel
170 P45 Prognostic modeling with the lasso: An empirical evaluation Steyerberg, E.W.
1997
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171 P98 Progression of carotid artery intima-media thickness predicts clinical coronary events LaBree, Laurie
1997
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172 P118 Prospective meta-analysis using individual patient data vs meta-analysis of published reports: The case of ace-inhibitors in myocardial infarction Franzosi, Maria Grazia
1997
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173 P111 Protocol enhancements for a study of alcohol-dependent patients Cramer, Joyce
1997
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174 P78 Pseudo-likelihood methods for general missing data mechanisms Michiels, Bart
1997
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175 P87 Q-Twist analyses of childhood cancer treatment regimens Gelber, Shari
1997
18 3S1 p. S164-S165
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176 P26 Quality control reporting for multi-center trials — a report from the cpcra DuChene, Alain
1997
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177 P50 Radiotherapy review in phase iii breast cancer clinical trials: Is there a need for the submission of portal films? Bryant, John
1997
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178 P14 Recurrent miscarriage study: How should data from women who do not become pregnant be handled? Karrison, Theodore
1997
18 3S1 p. S118-S119
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179 P63 Registers of clinical trials in the regulatory affairs process Strang, W.N.
1997
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180 P86 Revisions to the ncic ctg expanded common toxicity criteria (ECTC)1 — do these revisions facilitate collection of more meaningful toxicity data for cancer clinical trials? Bennett, Katherine
1997
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181 99 Propensity score techniques for estimating treatment effects in clinical trials with drop-outs D'Agostino Jr., Ralph B.
1997
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182 P55 Showing results of clinical trials Sztaniszláv, Daniel
1997
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183 P103 Since when does correlation imply valid substitution? Simpson, P.M.
1997
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184 P115 Software for exploration and modeling of meta-analyses DuMouchel, William
1997
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185 P36 stage migration in gastric cancer; its influence on survival Hermans, J.
1997
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186 P129 State-of-the-art in vision randomized controlled clinical trials Scherer, Roberta W.
1997
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187 P76 Statistical issues in systematic reviews of chronic diseases Ashby, Deborah
1997
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188 P117 Statistical issues in the meta-analysis of treatments for Alzheimer's disease Whitehead, Anne
1997
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189 P30 statistics and statisticians in european drug regulatory agencies: Unharmonized Jones, David
1997
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190 P107 Stochastic sensitivity analysis in markovian disease models Mocks, Joachim
1997
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191 P34 strategies for minimizing the effect of hormone assay variability on clinical trial results Friedman, Lisa Aronson
1997
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192 P124 Subjective pathology tumor grading: Impact on design and analysis of radiation therapy oncology group (RTOG) prostate trial 8531 Winter, Kathryn
1997
18 3S1 p. S186-S187
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193 P84 Summarizing symptoms reported in daily diaries of women in the postmenopausal estrogen/progestins intervention (PEPI) trial James, Margaret K.
1997
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194 P48 Summary roc curve approach to assess the role of prognostic factors in liver cirrhosis Morabito, Alberto
1997
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195 P35 the analysis of transformed count data in clinical trials Thompson, Bruce
1997
18 3S1 p. S131-S132
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196 P44 The association between birth weight and change in blood pressure: Should we adjust for adult body mass index? Hardy, Rebecca
1997
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197 P58 The benefits of an intranet as a coordinating center tool for multi-center research projects: The Epidemiology Data Center Intranet Martin, Jeffrey P.
1997
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198 P12 The changing face of tamoxifen treatment and its influence on attom Padmore, L.
1997
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199 P56 The clinical trials group's computerized data checking system Day, Andrew
1997
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200 P10 The delicate balance of filter-coagulation and patient hemorrhage with renal replacement procedures: Multivariate failure time data analysis. Zwinderman, Aeilko H.
1997
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201 P43 The Design And Analysis Of A Study With Outcome Dependent Sampling le Cessie, Saskia
1997
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202 P90 The problem with a heuristic approach to sample size estimation for time-to-failure endpoints involving three or more treatment groups Panzarella, Tony
1997
18 3S1 p. S166-S167
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artikel
203 P128 The sensitivity and yield of hand and medline searching for controlled trials in us general medical journals Reynolds, Matthew
1997
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204 P110 The statistical analysis of the agreement between the qualitative and quantitative clinical trial diagnostic devices Chiou, Wen-Jau
1997
18 3S1 p. S178-S179
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205 P122 The thrombolysis in acute stroke-pooling project: A prospective meta-analysis on individual patient data Boutitie, F.
1997
18 3S1 p. S185-
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206 P37 time series in clinical trials when can they be pooled? Dunstan, Frank
1997
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207 P81 Towards a utility-based assessment for cancer patients: Reliability and validity of the UBQ-C(ancer) items Martin, A.J.
1997
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208 P102 Unbiased trapezoidal estimation of area under curve from time response data with multiplicative exponential structure Jonsson, Robert
1997
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209 P41 Use of corrected P-values in selecting optimal cutpoints for prognostic factor studies Mazumdar, M.
1997
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210 P33 use of genotyping in clinical trials Wiklund, Kerstin
1997
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211 P85 Use of physician investigators for outcome review in the hemodialysis (HEMO) study 1997
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212 P23 use of the world wide web for clinical monitoring in multicenter clinical trials Schafer, Kimberly
1997
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213 P109 Using cluster analysis to identify risk groups for asthma morbidity among inner-city children Lynn, Henry
1997
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214 75 Retrospective, descriptive study of timeliness of clinical events reporting in a national HIV community-based clinical trials network Child, C.C.
1997
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215 57 Risk communication strategies during an ongoing clinical trial: Protecting participant safety without causing unnecessary panic, the breast cancer prevention trial (BCPT) experience Costantino, J.P.
1997
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216 51 Sample size and design considerations for phase II clinical trials with correlated observations Sargent, Daniel J.
1997
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217 103 Sample size calculation for clinical trials: The role of economic significance Campbell, Marion K.
1997
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218 S40 Estimation of rate of change in longitudinal studies with attrition with application in hiv clinical trials Toulomi, Giota
1997
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219 47 Sex differences in treatment of acute myocardial infarction Gardinale, E.
1997
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220 61 Significance level at treatment allocation by means of minimization Anderson, Harald
1997
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221 S38 Joint estimation of the mean and overdispersion parameters of an overdispersed poisson distribution using quasi-likelihood Bautista, Oliver M.
1997
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222 S36 Multiple endpoints en trials en HIV infection Walker, A.Sarah
1997
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223 S37 Practical properties of some structural mean analyses of the effect of compliance in randomized trials Lapp, Krista
1997
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224 S39 Statistical analysis of circadian blood pressure utilizing mixed models with smoothing splines MacDougall, James E.
1997
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225 50 Statistical arguments for the necessity of randomized trials in high-dose chemotherapy for breast cancer Schmoor, Claudia
1997
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226 12 Statistical methods to assess prognosis and to help treatment decision Ulm, K.
1997
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227 80 Structural failure time models for causal inference in clinical trials Loeys, Tom
1997
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228 59 Subversion of allocation in a randomised controlled trial Kennedy, Andrew
1997
18 3S1 p. S77-S78
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229 03 Surrogate endpoints for the prophylactic treatment of tat1 bladder cancer: A combined analysis of eortc and mrc randomized clinical trials 1997
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230 01 Surrogate endpoints in clinical trials: Some statistical perspectives Frison, Lars
1997
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231 27 Testing superiority of a combination therapy using prior information on the component treatments Farebrother, Joanna
1997
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232 21 The analysis of complex patterns of longitudinal binary response in clinical trials Thompson, Simon G.
1997
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233 102 The analysis of repeated multivariate binary data: Application of hierarchical models to quality of life data Beacon, Heather J.
1997
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234 06 The Clinical Trials Training Program (CTTP) at Memorial Sloan-Kettering Cancer Center Dean, Lorna K.
1997
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235 48 The impact on prevalence of dementia in the oldest age groups of differential mortality patterns McGee, M.A.
1997
18 3S1 p. S70-S71
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236 54 The use of a sample size review in a head injury trial with ordered categorical responses Bolland, Kim
1997
18 3S1 p. S74-S75
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237 02 The validation of surrogate endpoints in randomized clinical trials Molenberghs, Gert
1997
18 3S1 p. S41-S42
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238 65 Treatment comparisons controlling for multiple testing Brooks, Maria Mori
1997
18 3S1 p. S81-
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239 90 Use of fax in data management software in a multicentered, multinational trial: Experience of the hope study Bosch, Jackie
1997
18 3S1 p. S97-
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240 19 Utility of the enrollment period in the Prostate Cancer Prevention Trial (PCPT) Goodman, Phyllis J.
1997
18 3S1 p. S52-S53
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241 83 Web databases: Oh what a tangled web we weave Rushing, Scott
1997
18 3S1 p. S92-S93
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242 85 Web development for clinical trials: It's not just for-programmers anymore Bak, Sharon M.
1997
18 3S1 p. S93-S94
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243 92 Women's health initiative memory study: A trial of the effect of estrogen therapy in preventing dementia Melton, Beth
1997
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                             243 gevonden resultaten
 
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