Literature DB >> 4076336

A non-parametric confidence interval method.

A Racine-Poon, A P Grieve.   

Abstract

Mesh:

Year:  1985        PMID: 4076336     DOI: 10.1007/BF00544099

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


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  8 in total

Review 1.  Use of statistical methods in evaluation of in vivo performance of dosage forms.

Authors:  W J Westlake
Journal:  J Pharm Sci       Date:  1973-10       Impact factor: 3.534

2.  Bioavailability--a problem in equivalence.

Authors:  C M Metzler
Journal:  Biometrics       Date:  1974-06       Impact factor: 2.571

3.  Statistical aspects of comparative bioavailability trials.

Authors:  W J Westlake
Journal:  Biometrics       Date:  1979-03       Impact factor: 2.571

4.  Generalization of distribution--free confidence intervals for bioavailability ratios.

Authors:  V W Steinijans; E Diletti
Journal:  Eur J Clin Pharmacol       Date:  1985       Impact factor: 2.953

5.  The two-period cross-over clinical trial.

Authors:  M Hills; P Armitage
Journal:  Br J Clin Pharmacol       Date:  1979-07       Impact factor: 4.335

6.  Bayesian approach to bioequivalence assessment: an example.

Authors:  H Fluehler; A P Grieve; D Mandallaz; J Mau; H A Moser
Journal:  J Pharm Sci       Date:  1983-10       Impact factor: 3.534

7.  Statistical analysis of bioavailability studies: parametric and nonparametric confidence intervals.

Authors:  V W Steinijans; E Diletti
Journal:  Eur J Clin Pharmacol       Date:  1983       Impact factor: 2.953

8.  Pharmacokinetics of theophylline in patients following short-term intravenous infusion.

Authors:  V W Steinijans; R Eicke; J Ahrens
Journal:  Eur J Clin Pharmacol       Date:  1982       Impact factor: 2.953

  8 in total
  1 in total

1.  Evaluation of bioequivalence studies.

Authors:  A P Grieve
Journal:  Eur J Clin Pharmacol       Date:  1991       Impact factor: 2.953

  1 in total

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