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                             36 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Bayesian adaptive Phase I–II clinical trial for evaluating efficacy and toxicity with delayed outcomes Koopmeiners, Joseph S
2014
11 1 p. 38-48
artikel
2 A Bayesian adaptive Phase I–II clinical trial for evaluating efficacy and toxicity with delayed outcomes Koopmeiners, Joseph S
2014
11 1 p. 38-48
artikel
3 A phase I/II seamless dose escalation/expansion with adaptive randomization scheme (SEARS) Pan, Haitao
2014
11 1 p. 49-59
artikel
4 A phase I/II seamless dose escalation/expansion with adaptive randomization scheme (SEARS) Pan, Haitao
2014
11 1 p. 49-59
artikel
5 A randomized trial of the clinical utility of genetic testing for obesity: Design and implementation considerations Wang, Catharine
2014
11 1 p. 102-113
artikel
6 A randomized trial of the clinical utility of genetic testing for obesity: Design and implementation considerations Wang, Catharine
2014
11 1 p. 102-113
artikel
7 Beyond intention to treat: What is the right question? Shrier, Ian
2014
11 1 p. 28-37
artikel
8 Beyond intention to treat: What is the right question? Shrier, Ian
2014
11 1 p. 28-37
artikel
9 Bumps and bridges on the road to responsible sharing of clinical trial data Berlin, Jesse A
2014
11 1 p. 7-12
artikel
10 Bumps and bridges on the road to responsible sharing of clinical trial data Berlin, Jesse A
2014
11 1 p. 7-12
artikel
11 Clinical and Health Outcomes Initiative in Comparative Effectiveness for Bipolar Disorder (Bipolar CHOICE): A pragmatic trial of complex treatment for a complex disorder Nierenberg, Andrew A
2014
11 1 p. 114-127
artikel
12 Clinical and Health Outcomes Initiative in Comparative Effectiveness for Bipolar Disorder (Bipolar CHOICE): A pragmatic trial of complex treatment for a complex disorder Nierenberg, Andrew A
2014
11 1 p. 114-127
artikel
13 Clinician-trialist rounds: 19. Faux pas or fraud? Identifying centers that have fabricated their data in your multi-center trial Pogue, Janice
2014
11 1 p. 128-130
artikel
14 Clinician-trialist rounds: 19. Faux pas or fraud? Identifying centers that have fabricated their data in your multi-center trial Pogue, Janice
2014
11 1 p. 128-130
artikel
15 Commentary on Berlin et al. Fergusson, Dean A
2014
11 1 p. 13-14
artikel
16 Commentary on Berlin et al. Goldacre, Ben
2014
11 1 p. 15-18
artikel
17 Commentary on Berlin et al. Fergusson, Dean A
2014
11 1 p. 13-14
artikel
18 Commentary on Berlin et al. Goldacre, Ben
2014
11 1 p. 15-18
artikel
19 Corrigendum 2014
11 1 p. 133
artikel
20 Corrigendum 2014
11 1 p. 133-133
artikel
21 Editorial transition Begg, Colin B
2014
11 1 p. 5-6
artikel
22 Editorial transition Begg, Colin B
2014
11 1 p. 5-6
artikel
23 Expectations and experiences of investigators and parents involved in a clinical trial for Duchenne/Becker muscular dystrophy Peay, Holly L
2014
11 1 p. 77-85
artikel
24 Expectations and experiences of investigators and parents involved in a clinical trial for Duchenne/Becker muscular dystrophy Peay, Holly L
2014
11 1 p. 77-85
artikel
25 Marker Sequential Test (MaST) design Freidlin, Boris
2014
11 1 p. 19-27
artikel
26 Marker Sequential Test (MaST) design Freidlin, Boris
2014
11 1 p. 19-27
artikel
27 2013 Peer Reviewers 2014
11 1 p. 131-132
artikel
28 2013 Peer Reviewers 2014
11 1 p. 131-132
artikel
29 Satisfying the needs of Japanese cancer patients: A comparative study of detailed and standard informed consent documents Sato, Keiko
2014
11 1 p. 86-95
artikel
30 Satisfying the needs of Japanese cancer patients: A comparative study of detailed and standard informed consent documents Sato, Keiko
2014
11 1 p. 86-95
artikel
31 Survey of consent practices in cluster randomized trials: Improvements are needed in ethical conduct and reporting Taljaard, Monica
2014
11 1 p. 60-69
artikel
32 Survey of consent practices in cluster randomized trials: Improvements are needed in ethical conduct and reporting Taljaard, Monica
2014
11 1 p. 60-69
artikel
33 Understanding and retention of trial-related information among participants in a clinical trial after completing the informed consent process Mexas, Fernanda
2014
11 1 p. 70-76
artikel
34 Understanding and retention of trial-related information among participants in a clinical trial after completing the informed consent process Mexas, Fernanda
2014
11 1 p. 70-76
artikel
35 Use of health plan combined with registry data to predict clinical trial recruitment Curtis, Jeffrey R
2014
11 1 p. 96-101
artikel
36 Use of health plan combined with registry data to predict clinical trial recruitment Curtis, Jeffrey R
2014
11 1 p. 96-101
artikel
                             36 gevonden resultaten
 
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