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Monitoring and controlling refer to the continuous (or sequential) viewing of temperature and thermal effects occurring in the ablation zone during application of power and to the intra-procedural use of image-based feedback to modify the procedure (i.e. change electrode position or adapt energy delivery algorithm).
Dr Kleissl's innovations are to modify the procedure so that it can use off-the-shelf lasers, and to improve the software.
Therefore, we decided to modify the procedure in the way that the reflectance values at respective wavelengths were divided not by the continuum, but by the maximal reflectance value of the particular spectrum.
We increased mapping accuracy by de novo assembly and aligned 93.5%, 92.7%, 92.2% and 91.9% of WT, respectively, confirming the need to modify the procedure for the wild accessions.
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To overcome these drawbacks, Anitua developed plasma rich in growth factors (PRGF) by modifying the procedure of PRP preparation [2].
We modified the procedure by allowing only such shifts that do not increase overtime consumption, therefore, leading to schedules with possibly both decreased makespan and lowered overtime costs.
In the work reported here, we have modified the procedure for obtaining the textural features and proposed the scribble boosting technique, which eliminates the main drawbacks of these earlier algorithms.
Most recently, several clinicians modified the procedure by further reducing the flap size needed for the procedure, moving the access site to the ridge crest, and limit the access window to an implant osteotomy created with osteotomes [11, 12].
We modified the procedure used by Sharan et al. [33] to merge CPIMs.
This experiment was conceptually the same as Experiment 1, but we modified the procedure and apparatus to allow more detailed examination of the cognitive processes involved.
We modified the procedure described above to accommodate cultured mammalian cells (see Materials and Methods) and established that the procedure could detect uptake of both white (FIG. 1C) and opaque (FIG. 1D) cells of C. albicans.
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