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Distinct characteristics of antibody responses against factor VIII in healthy individuals and in different cohorts of hemophilia A patients

Blood, 2013-02, Vol.121 (6), p.1039-1048

2013

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The potential of the estimands framework for clinical pharmacology trials: Some discussion points

British journal of clinical pharmacology, 2020-07, Vol.86 (7), p.1240-1247

2020

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Assessment of pharmacokinetic linearity after repeated drug administration

Pharmaceutical statistics : the journal of the pharmaceutical industry, 2022-09, Vol.21 (5), p.932-943

2022

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Recurrent events modelling of haemophilia bleeding events

Journal of the Royal Statistical Society Series C: Applied Statistics, 2021-03, Vol.70 (2), p.351-371

2021

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Non-compartmental estimation of pharmacokinetic parameters for flexible sampling designs

Statistics in medicine, 2012-05, Vol.31 (11-12), p.1059-1073

2012

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Estimation in AB/BA crossover trials with application to bioequivalence studies with incomplete and complete data designs

Statistics in medicine, 2013-12, Vol.32 (30), p.5469-5483

2013

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Adjustment of endogenous concentrations in pharmacokinetic modeling

European journal of clinical pharmacology, 2014-12, Vol.70 (12), p.1465-1470

2014

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Authors' reply to Comments on 'Estimation in AB/BA crossover trials with application to bioequivalence studies with incomplete and complete data designs

Statistics in medicine, 2013-12, Vol.32 (30), p.5487-5488

2013

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Two-component polyethylene glycol surgical sealant influence on intraperitoneal infection in a refined rodent model

American journal of obstetrics and gynecology, 2010-11, Vol.203 (5), p.494.e1-494.e6

2010

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Assessing goodness‐of‐fit for evaluation of dose‐proportionality

Pharmaceutical statistics : the journal of the pharmaceutical industry, 2021-03, Vol.20 (2), p.272-281

2021

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hybrid method to estimate the minimum effective dose for monotone and non‐monotone dose–response relationships

Biometrics, 2014-03, Vol.70 (1), p.103-109

2014

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A comparison of methods for classifying samples as truly specific with confirmatory immunoassays

Journal of pharmaceutical and biomedical analysis, 2014-01, Vol.88, p.27-35

2014

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A formal comparison of different methods for establishing cut points to distinguish positive and negative samples in immunoassays

Journal of pharmaceutical and biomedical analysis, 2011-07, Vol.55 (5), p.1148-1156

2011

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Non-compartmental estimation of pharmacokinetic parameters in serial sampling designs

Journal of pharmacokinetics and pharmacodynamics, 2009-10, Vol.36 (5), p.479-494

2009

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A note on statistical analysis of organ weights in non-clinical toxicological studies

Toxicology and applied pharmacology, 2009-10, Vol.240 (1), p.117-122

2009

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A Theoretical Framework for Estimation of AUCs in Complete and Incomplete Sampling Designs

Statistics in biopharmaceutical research, 2009-05, Vol.1 (2), p.176-184

2009

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Establishing bioequivalence in serial sacrifice designs

Journal of pharmacokinetics and pharmacodynamics, 2007-02, Vol.34 (1), p.103-113

Wolfsegger, Martin J

2007

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Confidence intervals for ratios of AUCs in the case of serial sampling: a comparison of seven methods

Pharmaceutical statistics : the journal of the pharmaceutical industry, 2009-01, Vol.8 (1), p.12-24

2009

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Assessing Systemic Drug Exposure in Repeated Dose Toxicity Studies in the Case of Complete and Incomplete Sampling

Biometrical journal, 2009-12, Vol.51 (6), p.1017-1029

2009

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Establishing Bioequivalence in Complete and Incomplete Data Designs Using AUCs

Journal of biopharmaceutical statistics, 2010-07, Vol.20 (4), p.803-820

2010

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Estimation of pharmacokinetic parameters with the R package PK

Pharmaceutical Statistics, 2011-05, Vol.10 (3), p.284-288

2011

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Assessment of rVWF Pharmacokinetics in Overweight and Obese VWD Patients Using a Population Pharmacokinetic Model

Blood, 2020-11, Vol.136 (Supplement 1), p.7-8

2020

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Simultaneous confidence intervals by iteratively adjusted alpha for relative effects in the one-way layout

Statistics and computing, 2006-03, Vol.16 (1), p.15-23

2006

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Pharmacokinetics, disease-modifying activity, and safety of an experimental therapeutic targeting an immunological isoform of macrophage migration inhibitory factor, in rat glomerulonephritis

European journal of pharmacology, 2018-02, Vol.820, p.206-216

2018

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Safety of Baxter's Longer Acting rFVIII (BAX 855) After Repeated Application in Rats and Cynomolgus Monkeys

Blood, 2011-11, Vol.118 (21), p.4345-4345

2011

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Distinct characteristics of antibody responses against factor VIII in healthy individuals and in different cohorts of hemophilia A patients

The potential of the estimands framework for clinical pharmacology trials: Some discussion points

Assessment of pharmacokinetic linearity after repeated drug administration

Recurrent events modelling of haemophilia bleeding events

Non-compartmental estimation of pharmacokinetic parameters for flexible sampling designs

Estimation in AB/BA crossover trials with application to bioequivalence studies with incomplete and complete data designs

Adjustment of endogenous concentrations in pharmacokinetic modeling

Authors' reply to Comments on 'Estimation in AB/BA crossover trials with application to bioequivalence studies with incomplete and complete data designs

Two-component polyethylene glycol surgical sealant influence on intraperitoneal infection in a refined rodent model

Assessing goodness‐of‐fit for evaluation of dose‐proportionality

hybrid method to estimate the minimum effective dose for monotone and non‐monotone dose–response relationships

A comparison of methods for classifying samples as truly specific with confirmatory immunoassays

A formal comparison of different methods for establishing cut points to distinguish positive and negative samples in immunoassays

Non-compartmental estimation of pharmacokinetic parameters in serial sampling designs

A note on statistical analysis of organ weights in non-clinical toxicological studies

A Theoretical Framework for Estimation of AUCs in Complete and Incomplete Sampling Designs

Establishing bioequivalence in serial sacrifice designs

Confidence intervals for ratios of AUCs in the case of serial sampling: a comparison of seven methods

Assessing Systemic Drug Exposure in Repeated Dose Toxicity Studies in the Case of Complete and Incomplete Sampling

Establishing Bioequivalence in Complete and Incomplete Data Designs Using AUCs

Estimation of pharmacokinetic parameters with the R package PK

Assessment of rVWF Pharmacokinetics in Overweight and Obese VWD Patients Using a Population Pharmacokinetic Model

Simultaneous confidence intervals by iteratively adjusted alpha for relative effects in the one-way layout

Pharmacokinetics, disease-modifying activity, and safety of an experimental therapeutic targeting an immunological isoform of macrophage migration inhibitory factor, in rat glomerulonephritis

Safety of Baxter's Longer Acting rFVIII (BAX 855) After Repeated Application in Rats and Cynomolgus Monkeys

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