Journal of Chinese Integrative Medicine ›› 2011, Vol. 9 ›› Issue (11): 1185-1189.doi: 10.3736/jcim20111105
• Methodology • Previous Articles Next Articles
Liang-ping Hu(
), Xiao-lei Bao, Li-xin Tao, Shi-guo Zhou, Xue Guan
| [1] |
Hu LP, Zhou SG . Three special tests and their SAS realization for univariate quantitative data in the design of one factor with two levels. Zhongguo Yi Yao Sheng Wu Ji Shu. 2010; 5(6): 466-468. Chinese.
doi: 10.3969/cmba.j.issn.1673-713X.2010.06.016 |
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胡良平, 周诗国 . 成组设计一元定量资料的三种特殊检验及其SAS实现.中国医药生物技术. 2010; 5(6):466-468.
doi: 10.3969/cmba.j.issn.1673-713X.2010.06.016 |
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| [2] | Hu LP. SAS research design and statistical analysis. Beijing: People’s Medical Publishing House. 2010 : 219. Chinese. |
| 胡良平 . SAS实验设计与统计分析.北京: 人民卫生出版社. 2010: 219. | |
| [3] | Hu LP, Gao H. Guidance of statistical analysis by SAS. Beijing: Publishing House of Electronics Industrial. 2010: 690-706. Chinese. |
| 胡良平, 髙辉 . SAS统计分析教程.北京: 电子工业出版社. 2010: 690-706. | |
| [4] | Chow SC, Shao J, Wang HS. Sample size estimation in clinical research. 2nd ed. New York: CRC Press. 2003: 55-63. |
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Hauck WW, Anderson S . A new statistical procedure for testing equivalence in two-group comparative bioavailability trials. J Pharmacokinet Biopharm. 1984 ;12 (1): 83-91.
doi: 10.1007/BF01063612 |
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Schuirmann DJ . A comparison of the two one-sided tests procedure and the power approach for assessing the equivalence of average bioavailability. J Pharmacokinet Biopharm. 1987 ; 15(6): 657-680.
doi: 10.1007/BF01068419 |
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