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It is of interest to compare GERD-related productivity impairments in the RANGE study with findings from other studies in patients with chronic disorders, which have used modified versions of the WPAI questionnaire.
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Conversion increased with temperature almost linearly within the temperature range studied, with a slight decrease in selectivity to formaldehyde.
All samples show positive RH for the entire temperature range studied, with carrier concentrations ranging from 9.6 × 1020 to 2.8 × 1021 cm−3 at room temperature.
The apparent second-order rate constant follows an Arrhenius temperature dependence over the range studied with an activation energy of 3.36×104 kJ/kmol.
These results demonstrate that these two primer probe sets generate linear results over the expression range studied, with R2 values close to 1 being obtained.
Studies on the effects of sociodemographic variables in subjects without brain injury show a strong educational effect on performance in the TT, but the effect of aging is controversial, depending on the version of the test employed, the scoring system used, and the age range studied, with decline being most evident beyond 65 years of age [ 21, 27– 30].
A VI dose-ranging study with concurrent ICS, also in persistent asthma, showed that the 25-μg dose of VI administered once daily over 4 weeks provided the most beneficial therapeutic ratio.
Indeed, similar results had been reported in the C204 dose-ranging study, with increases in LDL cholesterol and triglycerides that were significantly higher in the efavirenz group than in the rilpivirine group after 96 weeks.
4 The same trends were also seen in the C204 dose-ranging study, with rash of any type being more common in the rilpivirine 150 mg and 75 mg groups than in the 25 mg group.
In contrast, in a recent dose-ranging study with another prostaglandin analog, bimatoprost 0.01% was found to be equivalent in efficacy to 0.03% bimatoprost, while, surprisingly, bimatoprost 0.0125% was not as effective [ 23].
Given the mixed findings in this group of subjects, larger, parallel design dose ranging studies with NS2359 using higher doses are warranted.
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