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Similar findings have been reported in several other studies for the evaluation of LAMP assay when compared against the qPCR [ 46, 47].
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For development and evaluation of the orfX-LAMP assay, 116 reference strains were included, with various species of gram-negative and -positive isolates (Table 1).
The samples were divided in the laboratory to be used for routine diagnosis by serological assays and evaluation of the RT-LAMP assay developed in this study.
Finally, since bilateral cases of ICE syndrome have been reported and subclinical changes have been also described in the contralateral unaffected eye, a careful examination of the fellow eye should be performed, including slit-lamp evaluation of the anterior segment structures, gonioscopy, tonometry, and endothelium evaluation by specular and/or in vivo confocal microscopy [ 45– 45].
Fig. 11 Cutouts of the checkerboard in the lamp scene, evaluation of ISO settings for EVS M = 2, Γ = 1.0.
(Bottom row) From left to right: dualISO 100 3200, dualISO 100 6400, dualISO 100 12800, and dualISO 100 25600 Fig. 12 Cutouts of the glass in the lamp scene, evaluation of ISO settings for EVS M = 2, Γ = 1.0.
Comparison of our method with EVS rule M = 2; Γ = 1.0 for different gain patterns: block pattern, row pattern, and diagonal pattern Fig. 10 Lamp scene, evaluation of EVS, and ICI method for different degrees of polynomial for dualISO 100 1600 with row pattern from left to right with M = 0, 1, and 2.
During the dispensing visits, the participants underwent slit lamp examination, evaluation of NIBUT with and without CL and BUT.
The subsequent clinical examination included a comprehensive anterior segment evaluation, including slit lamp biomicroscopy, evaluation of lid margin thickness and hyperemia, conjunctival erythema, chemosis, tear film debris and mucus, and extent of meibomian gland plugging.
The evaluation of the lifetime of fluorescent lamps and electronic ballast is a current issue in illuminating engineering.
The studies conducted in Poland involved a 3-week application period, with ophthalmological assessment by slit-lamp and evaluation of subjective functional signs before and after use on day 21 and subjective self-assessment patient questionnaires regarding functional/physical signs.
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