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Significantly improved ADHD symptom scores (versus placebo) based on randomized, placebo-controlled trials using long-acting formulations of either methylphenidate (MPH) [ 3, 4] or amphetamines have been reported [ 5, 6].
In the IR phase, patients received IR formulations of either hydromorphone [Dilaudid®, Abbott Laboratories] or morphine (morphine sulfate IR [Sevredol®, Napp Laboratories]) every 4 hours (6 times daily) for 2 to 9 days.
The literature search identified twelve publications for three different products: two microsphere-based leuprorelin acetate formulations of either 30 mg or 45 mg dose depots and a gel-based leuprorelin acetate 45 mg dose depot formulation.
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4 groups (10 participants each group) received the vaccine formulation of either 20 µg, 50 µg, 100 µg or 200 µg while the fifth (12 participants) received placebo.
If a stochastic SIRS model (in the formulation of either stochastic differential equations or continuous-time Markov Chain) was used in ABC, the credible intervals would be wider due to the addition of stochasticity into the SIRS model.
Probabiliorism, which enjoins following the more probable opinion, was predominant in the 18th century before the formulation of equiprobabilism (either of two equally probable opinions may be followed) by the moral theologian Alfonso Maria de Liguorii, a doctor of the Roman Catholic church.
In Botstein and Campbell's formulation, modules (composed of either a single gene or more often a group of functionally related ones) are exchanged via flanking conserved "linker" sequences that ensure both the proper placement and regulation of the module in its new phage genomic context (Botstein 1980).
Practical experience comes to testify that this diversity can be enriching when reviewing the formulation of either the questions or the answer categories and can even lead to the inclusion of additional questions and/or answering categories.
Based on new clinical data demonstrating that the effects with a single treatment of either formulations may last for up to 12 months, the FDA have granted a label extension for Juvéderm™ Ultra and Juvéderm™ Ultra Plus in June, 2007 (Allergan, Inc. 2007).
At 8 am each person received a single oral dose of 500 mg of either formulation.
We conclude that under conditions pertaining in this study, a single subcutaneous injection of a moxidectin SR formulation at dosing rates of either 0.17 or 0.27 mg/kg b.w.
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