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The effect of using hydrophilic monomers of acrylic acid (AAc), methacrylic acid (MAAc), dimethyl acrylamide (DMAAm), and hydroxyethyl methacrylate (HEMA) for the copolymerization on the critical point was evaluated.
Change in BF LAB) (or BF LAB) volume) at any point was evaluated by difference between change in BF(Ao) and in BF FAs).
The "branch point " was evaluated after magnifying the slices.
Each end point was evaluated quantitatively using several methods.
Therefore, this cut-off point was evaluated for TILC in all subsequent analyses in this study.
Each time point was evaluated separately relative to the baseline value.
The primary end point was evaluated with ANCOVA at the level of α = 0.025 (one-sided).
The risk for the primary end point was evaluated by using the Cox proportional hazards model (Table 2).
Arterial cross section area for each time point was evaluated using a threshold of 10% above the maximum speed value in a data set.
Because each end point was evaluated relative to an isogenic control cohort, the approach did not weaken the ability to detect effects but actually strengthened the method.
The number of injections required at each calibration point was evaluated in 91 hemodynamically stable patients monitored by a PiCCO2 device (Pulsion, Munich, Germany) [ 20].
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