1. |
Moher D, Schulz KF, Altman DG. The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomized trials. Lancet, 2001, 357: 1191-1194.
|
2. |
Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med, 2009, 151(4): 264-269.
|
3. |
Fernández E. Observational studies in Epidemiology (STROBE). Med Clin (Barc), 2005, 125(Supl.1): 43-48.
|
4. |
Ad Hoc Working Group. A proposal for more informative abstracts of clinical articles. Annual of Internation Medicine, 1987, 106: 598-604.
|
5. |
Standards of Reporting Trials Group. A proposal for structured reporting of randomized controlled trials. JAMA, 1994, 272(24): 1926-1931.
|
6. |
Working group on recommendations for reporting of clinical trials in the biomedical literature. Call for comments on a proposal to improve reporting of clinical trials in the biomedical literature: a position paper. Ann Intern Med, 1994, 121(11): 894-895.
|
7. |
Begg C, Cho M, Eastwood S, et al. Improving the quality of reporting of randomized controlled trials. JAMA, 1996, 276(8): 637-639.
|
8. |
Extensions of the CONSORT Statement. [2010-01-03]. http://www. consort-statement.org/extensions/.
|
9. |
杜亮, 陈耀龙, 陈敏, 等. 从CONSORT到GPP: 医学研究报告规范简介. 编辑学报, 2008(4): 367-370.
|
10. |
Laine C, Horton R, DeAngelis C, et al. International Committee of Medical Journal Editors (ICMJE). Clinical trial registration: looking back and moving ahead. Lancet, 2007, 369(9577): 1909-1911.
|
11. |
Ghersi D, Pang T. 从墨西哥到马里: 临床试验注册发展历程四年回顾. 中国循证医学杂志, 2009, 9(2): 123-126.
|