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An acceptable phase bandwidth range within ± 10° was obtained when L2 = 365 nm for RCP, and L2 = 450 nm for LCP, as shown in Fig. 4c.
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The results present the acceptable phase retardation range of polarization controllers composed of two quarter-wave plates or a quarter-half-quarter-wave plate combination, and thereby determines the operation wavelength range of a given design.
We further prove that a quarter-quarter-half-wave-plate combination is also an arbitrary birefringence compensator as well as a conventional quarter-half-quarter-wave-plate combination, and show that the two configurations have the identical range of acceptable phase retardance within the uncertainty of our numerical method.
The models of the best-fit and acceptable phase velocity curves are shown in Fig. 3b.
Therefore, the acceptable phase velocity curves, which differ by 1% from the curve that best fits the observation, were plotted.
Of the 1,028 DCCT/EDIC participants, 879 (86.4%) had technically acceptable phase-contrast cine aorta MRI (Supplementary Fig. 1).
Limits may be defined on the acceptable phases of the respiratory cycle for the treatment to be delivered and the software may then gate the treatment delivery automatically.
S-1 showed response rates of 28.8% to 46.2% with an acceptable toxicit in phase II studies of advanced and recurrent HNSCC [ 29, 30].
The new notions of 'solubility diagram', 'solidus', 'liquidus', and 'nanophase diagram' outlined here provide an acceptable description of the phase transition phenomenon in a nanosystem.
As a result, placebo has remained as an acceptable control in randomised phase III trials until sorafenib (Nexavar; Bayer HealthCare AG, Leverkusen, Germany) was shown to improve the survival of advanced HCC over placebo in both Caucasian and Asian populations (Llovet et al, 2008; Cheng et al, 2009).
During the course of the trial, independent groups conducted modeling studies to determine whether the change in the sum of the longest dimensions of target lesions for NSCLC at 8 weeks of therapy would be an acceptable primary endpoint for phase II clinical trials [ 19, 20, 22].
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