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The results of a parametric formulation conducted introducing key parameters for the design procedure of the fuse system, validated by nonlinear time history analyses are presented.
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This trend was further confirmed during a bioequivalence study of two pemetrexed formulations conducted in our center.
Targeted engagement of potential end-users in the formulation, conduct and interpretation of research, sustainable interaction, trust, and active engagement of researchers in health decision making processes, all seem to have enhanced the use of results to contribute to action.
Theoretically, participatory action research involves all potential users of the research in the formulation, conduct, and application of the research and the research occurs in phased cycles (problem diagnosis, action planning, taking action, evaluating the actions, incorporating lessons, repeat) [ 18, 19].
Also, extension of the local formulation is conducted for an elastoplastic problem.
Clinical trials (including dose-ranging, pharmacokinetic/pharmacodynamic, and contraceptive efficacy studies) indicating the effectiveness of this new formulation were conducted primarily in white women.
Although the formulation is conducted using the lead lanthanum zirconate titanate ceramics (PLZT) polarized in 0-3 direction subjected to light illumination and mechanical loading, the results may be extended to other photostrictive materials or degenerated to piezoelectric ceramics.
Due to lack of appropriate results for free vibration of CGCNTR cylindrical panels reinforced by oriented CNTs for direct comparison, validation of the presented formulation is conducted in two ways.
The total dissolution time and risk assessment for the IV formulation was conducted by measuring the plasma solubility of DCU, particle size of the nanoparticles and the diffusion coefficient of DCU in rat plasma.
A large study with the paediatric dose (0.25 mL) of the adult formulation RTS,S/AS02A, conducted in Mozambican children aged 1 4 years, demonstrated the vaccine to have an acceptable safety profile and to be efficacious against clinical malaria (vaccine efficacy of 35%) and severe malaria disease (vaccine efficacy of 49%) over a period of 18 months [6].
To compare the results given by the MDP and the LP formulations, we conducted experiments with the two scenarios described in "Improving solutions to the LP formulation" section.
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