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Furthermore, the efficacy analysis was updated to reflect endpoints that have recently been recommended to better differentiate among treatments in clinical trials of TTH, i.e. pain-free after 2 h (Y/N) and headache response after 2 h (Y/N) [11, 12].
The database that we used for our analysis was updated in May 2002.
The dataset used in this analysis was updated to include the spring 2010 climbing season.
Since that analysis, the mixed model used to produce the phenotypic inputs to the analysis was updated to better adjust for the effect of flowering time on SLB resistance phenotypes.
Pathology data from 12 of these studies has been previously published (Blows et al, 2010) and the analysis was updated to include data from another 3 studies excluded from the previous publication because of missing data on basal markers that is not relevant for this analysis (Table 1).
Figure 1 depicts a best-fit line for total doxorubicin concentration time data in patient #1 (PEG-LD 8 mg m−2) during cycles 1 and 2. Maximum-likelihood analysis was updated and two iterations were required to achieve stable estimates of the median parameters.
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Data for this analysis are updated as of 11 January 2012.
Surveys used to conduct this analysis were updated and mailed biennially, and had a > 90% response in each questionnaire cycle.
Follow-ups for all patients included in the survival analysis were updated in January 25, 2003 (median follow-up time was 103 months; range, 60 144 months).
Although it would take a large study with a strongly positive result to cause a noticeable increase in effect size, the limited number of studies and relatively low overall numbers of participants could reduce the robustness of our findings, and as results from further studies become available it is important that this analysis is updated.
To determine the value of cervicovaginal fetal fibronectin as a marker for preterm delivery, a previously published meta-analysis was updated.
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