| 臺大學術典藏 |
2018-09-10T06:57:52Z |
Design and Analysis of Clinical Trials: Concepts and Methodologies
|
Jen-Pei Liu; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:52Z |
Design and Analysis of Clinical Trials: Concepts and Methodologies
|
Jen-Pei Liu; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:51Z |
On statistical evaluation of the linearity in assay validation
|
Hsieh, E.;Liu, J.-P.; Hsieh, E.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:51Z |
Commentary on "accounting for the interim safety monitoring of an adverse event upon termination of a clinical trial"
|
Liu, J.-P.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:51Z |
A two-stage design for drug screening trials based on continuous endpoints
|
Tsou, H.-H. and Hsiao, C.-F. and Chow, S.-C. and Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:50Z |
Statistical methods for targeted clinical trials under enrichment design.
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Liu, J.P.;Lin, J.R.; Liu, J.P.; Lin, J.R.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:50Z |
Statistical issues on the diagnostic multivariate index assay for targeted clinical trials
|
Liu, J.-P.;Chow, S.-C.; Liu, J.-P.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:57:50Z |
Statistical evaluation of quality performance on genomic composite biomarker classifiers.
|
Liu, J.P.;Lu, L.T.; Liu, J.P.; Lu, L.T.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:56:57Z |
A non-inferiority test for diagnostic accuracy based on the paired partial areas under ROC curves
|
Li, C.-R.;Liao, C.-T.;Liu, J.-P.; Li, C.-R.; Liao, C.-T.; Liu, J.-P.; JEN-PEI LIU; CHEN-TUO LIAO |
| 臺大學術典藏 |
2018-09-10T06:56:56Z |
On the exact interval estimation for the difference in paired areas under the ROC curves
|
Li, C.-R.;Liao, C.-T.;Liu, J.-P.; Li, C.-R.; Liao, C.-T.; Liu, J.-P.; JEN-PEI LIU; CHEN-TUO LIAO |
| 臺大學術典藏 |
2018-09-10T06:56:56Z |
A permutation two one-sided tests procedure to detect minimal fold changes of gene expression levels
|
Liu, J.-P.;Liao, C.-T.;Chiu, S.-T.;Dai, J.-Y.; Liu, J.-P.; Liao, C.-T.; Chiu, S.-T.; Dai, J.-Y.; JEN-PEI LIU; CHEN-TUO LIAO |
| 臺大學術典藏 |
2018-09-10T06:24:53Z |
Some thoughts on individual bioequivalence
|
Liu, J.;Chow, S.-C.; Liu, J.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:24:53Z |
Meta-analysis for bioequivalence review
|
Chow, S.-C.;Liu, J.; Chow, S.-C.; Liu, J.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:24:53Z |
A two one-sided tests procedure for assessment of individual bioequivalence
|
Liu, J.;Chow, S.-C.; Liu, J.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:24:52Z |
Rethinking statistical approaches to evaluating drug safety
|
Liu, J.-P.; Liu, J.-P.; JEN-PEI LIU; Liu, Jen-pei |
| 臺大學術典藏 |
2018-09-10T06:24:52Z |
Statistical evaluation of similarity factor f2 as a criterion for assessment of similarity between dissolution profiles
|
Liu, J.-P.;Ma, M.C.;Chow, S.-C.; Liu, J.-P.; Ma, M.C.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T06:23:57Z |
Noninferiority tests based on concordance correlation coefficient for assessment of the agreement for gene expression data from microarray experiments
|
Liao, C.-T.;Lin, C.-Y.;Liu, J.-P.; Liao, C.-T.; Lin, C.-Y.; Liu, J.-P.; JEN-PEI LIU; CHEN-TUO LIAO |
| 臺大學術典藏 |
2018-09-10T05:53:08Z |
Test of equivalence and non-inferiority for diagnostic accuracy based on the paired areas under ROC curves
|
Liu, J.-P.;Ma, M.-C.;Wu, C.-Y.;Tai, J.-Y.; Liu, J.-P.; Ma, M.-C.; Wu, C.-Y.; Tai, J.-Y.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:53:08Z |
Statistical issues on the FDA conjugated estrogen tablets bioequivalence guidance
|
Liu, J.-P. and Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Statistical Design and Analysis in Pharmaceutical Science: Validation, Process Controls, and Stability
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Statistical Design and Analysis in Pharmaceutical Science: Validation, Process Controls, and Stability
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Statistical Design and Analysis in Pharmaceutical Science: Validation, Process Controls, and Stability
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
The impact of outlying subjects on decision of bioequivalence
|
Ki, F.Y.C.;Liu, J.-P.;Wang, W.;Chow, S.-C.; Ki, F.Y.C.; Liu, J.-P.; Wang, W.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Replicated crossover designs in bioavailability and bioequivalence trials
|
Liu, J.-P.;Chow, S.-C.; Liu, J.-P.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Current issues in bioequivalence trials
|
Chow, S.-C.;Liu, J.-P.; Chow, S.-C.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:18Z |
Bias of two one-sided tests procedures in assessment of bioequivalence
|
Liu, J.-P.;Weng, C.-S.; Liu, J.-P.; Weng, C.-S.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:17Z |
Tests for equivalence based on odds ratio for matched-pair design
|
Liu, J.-P.;Fan, H.-Y.;Ma, M.-C.; Liu, J.-P.; Fan, H.-Y.; Ma, M.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:17Z |
A two-stage design for bridging studies
|
Hsiao, C.-F.;Xu, J.-Z.;Liu, J.-P.; Hsiao, C.-F.; Xu, J.-Z.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:18:17Z |
Use of the repeated cross-over designs in assessing bioequivalence
|
Liu, J.-P.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T05:03:21Z |
High incidence rate of hip fracture in Taiwan: Estimated from a nationwide health insurance database
|
Chie, W.C.;Yang, R.S.;Liu, J.P.;Tsai, K.S.; Chie, W.C.; Yang, R.S.; Liu, J.P.; Tsai, K.S.; KEH-SUNG TSAI; RONG-SEN YANG; JEN-PEI LIU; WEI-CHU CHIE |
| 臺大學術典藏 |
2018-09-10T04:49:26Z |
A Bayesian noninferiority approach to evaluation of bridging studies
|
Liu, J.-P.;Hsueh, H.;Hsiao, C.-F.; Liu, J.-P.; Hsueh, H.; Hsiao, C.-F.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:49:26Z |
Recent statistical developments in bioequivalence trials - A review of the FDA guidance
|
Chow, S.-C.;Liu, J.-P.; Chow, S.-C.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:49:26Z |
Design and Analysis of Clinical Trials, second edition
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:49:26Z |
Design and Analysis of Clinical Trials, second edition
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:49:26Z |
Design and Analysis of Clinical Trials, second edition
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:49:25Z |
Bridging bioequivalence studies
|
Liu, J.-P.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:43:11Z |
Better Prediction of Prognosis for Patients with Nasopharyngeal Carcinoma Using Primary Tumor Volume
|
Chen, M.-K.;Chen, T.H.-H.;Liu, J.-P.;Chang, C.-C.;Chie, W.-C.; Chen, M.-K.; Chen, T.H.-H.; Liu, J.-P.; Chang, C.-C.; Chie, W.-C.; HSIU-HSI CHEN; JEN-PEI LIU; WEI-CHU CHIE |
| 臺大學術典藏 |
2018-09-10T04:29:18Z |
The design, contents, operation and the characteristics of the respondents of the 2001 National Health Interview Survey in Taiwan
|
Shih, Y.-T.;Hung, Y.-T.;Chang, H.-Y.;Liu, J.-P.;Lin, H.-S.;Chang, M.-C.;Chang, F.-C.;Hsiung, C.A.;Wu, S.-L.; Shih, Y.-T.; Hung, Y.-T.; Chang, H.-Y.; Liu, J.-P.; Lin, H.-S.; Chang, M.-C.; Chang, F.-C.; Hsiung, C.A.; Wu, S.-L.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:29:18Z |
Simultaneous non-inferiority test of sensitivity and specificity for two diagnostic procedures in the presence of a gold standard
|
Chen, J.J.;Hsueh, H.-M.;Liu, J.-P.; Chen, J.J.; Hsueh, H.-M.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:29:18Z |
Common statistical problems in public health research articles
|
Liu, J.-P.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:29:18Z |
A randomized trial comparing intravesical instillations of mitoxantrone and doxorubicin in patients with superficial bladder cancer
|
Huang, J.-S.;Chen, W.H.;Lin, C.-C.;Liaw, C.-C.;Wang, C.-H.;Lan, Y.-J.;Lai, C.-H.;Liu, J.-P.; Huang, J.-S.; Chen, W.H.; Lin, C.-C.; Liaw, C.-C.; Wang, C.-H.; Lan, Y.-J.; Lai, C.-H.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:29:18Z |
A group sequential approach to evaluation of bridging studies
|
JEN-PEI LIU; Liu, J.-P.; Hsiao, C.-F.;Xu, J.-Z.;Liu, J.-P.; Hsiao, C.-F.; Xu, J.-Z. |
| 臺大學術典藏 |
2018-09-10T04:29:18Z |
Evaluation of parametric and nonparametric two one-sided tests procedures for assessing bioequivalence of average bioavailability
|
Liu, J.-P.;Weng, C.-S.; Liu, J.-P.; Weng, C.-S.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:29:17Z |
The National Health Interview Survey information system: An overview
|
Lin, T.-H.;Chang, H.-Y.;Weng, W.-S.;Chen, Y.-J.;Cho, E.-Y.;Hsiung, C.A.;Liu, J.-P.; Lin, T.-H.; Chang, H.-Y.; Weng, W.-S.; Chen, Y.-J.; Cho, E.-Y.; Hsiung, C.A.; Liu, J.-P.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:09:27Z |
Design and Analysis of Bioavailability and Bioequivalence Studies
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:09:27Z |
Design and Analysis of Bioavailability and Bioequivalence Studies
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:09:27Z |
Design and Analysis of Bioavailability and Bioequivalence Studies
|
JEN-PEI LIU; JEN-PEI LIU; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:09:26Z |
Sample size determination for the two one-sided tests procedure in bioequivalence
|
Liu, J.-p.;Chow, S.-C.; Liu, J.-p.; Chow, S.-C.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:09:26Z |
Sample size requirements for evaluation of bridging evidence
|
Liu, J.-P.;Hsueh, H.;Chen, J.J.; Liu, J.-P.; Hsueh, H.; Chen, J.J.; JEN-PEI LIU |
| 臺大學術典藏 |
2018-09-10T04:09:26Z |
Bridging studies in clinical development
|
Liu, J.-P.; Chow, S.-C.; JEN-PEI LIU; Liu, J.-P.;Chow, S.-C. |
