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The recent Society for Healthcare Epidemiology of America (SHEA)/Infectious Diseases Society of America IDSAA) guidelines give interim recommendations for determination of severity based on white blood cell count and serum creatinine level [ 11]; however, a validated severity score is still needed [ 12].
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The data that we report do not support the recommendation for determination of MSI status in stage II CRC patients.
Recommendations for the determination of strength and flexibility of the end anchorages provided by welded shear stud connectors and mechanically attached shear transfer devices are presented.
Our objectives were (1) to identify potential sources of analytical variations of cytokine measurement within and among independent laboratories based on biological matrix and assay type and (2) to establish recommendations for cytokine determination, data analysis, and interpretation.
Past proficiency panels have focused on various aspects of the ELISPOT technology including first harmonization guidelines for assay conduct [ 10, 11], recommendations for response determination [ 12], a framework for structured reporting of T-cell assay results [ 13], as well as systematic studies of the impact of different test media on assay results [ 14, 15].
Neither the American Psychiatric Association or American pediatric guidelines [ 9] nor the NICE guidelines provide a clear recommendation for the determination of target weight.
Current recommendations for a priori determination of the number of subjects to include in a study suggest the inclusion of sufficient subjects to maintain adequate statistical power to detect a clinically meaningful effect size [ 34].
Various recommendations and formulations relevant for determination of the rational stiffened plate design (with respect to the considered problem) are proposed.
Other men suggested that social and cultural practices negatively influenced their determination to follow recommendations for healthy habits.
Serum was subjected to enzyme-linked immunosorbent assay (ELISA) for determination of IL-1β and TNF-α contents according to the manufacturers recommendations.
The methodology for determination of the reference intervals for plasma sulfate and FEI sulfate has been based on the recommendations from the International Federation of Clinical Chemistry [ 31].
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