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10.1007/s11222-021-10029-3

Min-max crossover designs for two treatments binary and poisson crossover trials


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10.1101/2021.01.13.21249779

Evaluating the Long-Term Efficacy of COVID-19 Vaccines


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10.1101/2021.02.09.430392

tDCS modulates effective connectivity during motor command following; a potential therapeutic target for disorders of consciousness



Control of Weekly Time Trend in Time-Stratified Case-Crossover Design


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10.9734/jsrr/2021/v27i930440

Bayesian Analysis of an Optimal Five Period Cross-over Design


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10.1177/17407745211028581

Design and analysis of a 2-year parallel follow-up of repeated ivermectin mass drug administrations for control of malaria: Small sample considerations for cluster-randomized trials with count data



Variability and effect sizes of intracranial current source density estimations during pain: Systematic review, experimental findings, and future perspectives



Measuring progress to healing: A challenge and an opportunity.


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10.1186/s12874-021-01322-w

RITS: a toolbox for assessing complex interventions via interrupted time series models


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10.1016/j.jspi.2020.12.002

Optimal crossover designs for inference on total effects


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10.1504/ijdmb.2021.10039923

Evaluation of statistical methods for the analysis of crossover designs with repeated measurements



Comparison of chronic kidney disease trial designs and analysis strategies



Approximate and exact designs for total effects


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10.1007/978-1-0716-1138-8_12

Randomized Controlled Trials 2: Analysis.



Pharmacokinetics and Safety of Dapoxetine Hydrochloride in Healthy Chinese Men: Impact of Dose and High‐Fat Meal


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10.21203/RS.3.RS-322376/V1

RITS: A Toolbox for Assessing Complex Interventions via Interrupted Time Series Models



Impact of study design and statistical model in pharmacogenetic studies with gene‐treatment interaction


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10.1016/j.apmr.2019.09.003

Functional Balance and Postural Control Improvements in Patients with Stroke after Non-Invasive Brain Stimulation: A Meta-Analysis.



Bioequivalence Assessment of Topical Ophthalmic Drugs Using Sparse Sampling Pharmacokinetics Data.


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10.1007/s40262-019-00778-w

Comment on: “Levothyrox® New and Old Formulations: Are they Switchable for Millions of Patients?”


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10.1136/bmjopen-2018-026478

Methodological advantages and disadvantages of parallel and crossover randomised clinical trials on methylphenidate for attention deficit hyperactivity disorder: a systematic review and meta-analyses



Accounting for a decaying correlation structure in cluster randomized trials with continuous recruitment.


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10.3389/fimmu.2019.01178

Tear Lactoferrin and Lysozyme as Clinically Relevant Biomarkers of Mucosal Immune Competence


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10.1007/s10928-019-09661-4

Impact of Phase 1 study design on estimation of QT interval prolongation risk using exposure–response analysis


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10.1007/s00702-019-02103-y

The emergence of animal models of chronic pain and logistical and methodological issues concerning their use


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10.1016/j.appet.2018.10.007

The effects of reward and loss anticipation on attentional bias for reward-related stimuli


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10.1186/s13063-019-3724-6

Sample size re-estimation in crossover trials: application to the AIM HY-INFORM study


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10.1080/00949655.2019.1575381

Nonparametric approaches for comparing three-period, two-treatment, four-sequence crossover designs



Comparison of crossover and parallel‐group designs for the identification of a binary predictive biomarker of the treatment effect


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10.1186/s12984-019-0562-4

Does transcranial direct current stimulation improve functional locomotion in people with Parkinson’s disease? A systematic review and meta-analysis


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10.22037/jps.v10i1.16352

Management of Baseline Measurements in Statistical Analysis of 2×2 Crossover Trials


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10.1007/s10664-019-09747-0

Meta-analysis for families of experiments in software engineering: a systematic review and reproducibility and validity assessment


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10.1080/10543406.2019.1684311

Optimal and/or efficient three treatment crossover designs for five carryover models



Power Analysis and Sample Size Determination for Crossover Trials with Application to Bioequivalence Assessment of Topical Ophthalmic Drugs Using Serial Sampling Pharmacokinetic Data.



Bioequivalence of Ertugliflozin/Sitagliptin Fixed‐Dose Combination Tablets and Coadministration of Respective Strengths of Individual Components



Effect of whole-grain consumption on changes in fecal microbiota: a review of human intervention trials.


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10.1007/s40279-019-01212-8

Reply to Borszcz & de Lucas: Comment on: “Effects of Carbohydrate Mouth Rinse on Cycling Time Trial Performance: A Systematic Review and Meta-Analysis”


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10.3390/healthcare7040137

Comparison of Aggregated N-of-1 Trials with Parallel and Crossover Randomized Controlled Trials Using Simulation Studies


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10.1136/bjsports-2018-100328

Precision exercise medicine: understanding exercise response variability



CONSORT 2010 statement: extension to randomised crossover trials


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10.1177/0962280219881026

Commentary to the recent study by Wang et al.


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