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Baseline samples were compared to on therapy results by two-tailed paired t-tests, with a P-value <0.05 taken as significant.
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Baseline serum samples were compared with samples drawn 1 year later for 50 women assigned to active hormone therapy in both the estrogen-plus-progestin and estrogen-alone randomized trials, by applying an in-depth proteomic discovery platform to serum pools from 10 women per pool.
Both the as-clad and post-heat treated (PHT) samples were compared to a baseline sample with an artificial notch to simulate damaged condition.
For comparisons relative to other neurological conditions, baseline SF-36 scores for the study sample were compared with other published scores for populations with Parkinson's disease and multiple sclerosis.
Animals were given a 3-h stabilization period, before baseline samples were being collected (four samples).
On the testing day, animals were given a 3-h stabilization period, before baseline samples were being collected (four samples).
In the proposed CRCNN framework, not only the input image is used, but also several other reference images are taken as baseline samples to be compared with the input.
Baseline characteristics were compared with independent samples t tests and χ analysis for continuous and categorical variables, respectively.
For the acute phase sample, for each instrument, baseline characteristics were compared between patients who had missing scores on all domains of the instrument during any acute phase visit and patients with non-missing values on at least one domain at all acute phase visit.
Groups' baseline characteristics were compared with independent sample t-tests.
The baseline demographics were compared using two-sample T-test for all continuous variables and Fisher's Exact test for categorical variables.
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