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It is worth mentioning that 17 physicians were evaluated in all three rounds of evaluation.
Medicaid reimbursement criteria for sofosbuvir were evaluated in all 50 states and the District of Columbia.
This design is evaluated in all minterms.
Complications were evaluated in all cases.
Toxicity was evaluated in all treatment groups except 227Th-rituximab.
Consistent with the in vitro cytotoxicity assay, caspase-3 activity was evaluated in all aforementioned groups.
The occurrence of adverse effects or complications was concomitantly evaluated in all patients.
The proportional hazards assumption was evaluated in all of the simulations.
ADM_12 treatment prevented the NTG-induced increasing of all genes evaluated in all areas (Fig. 2).
At the end of ventilation, mean arterial pressure (MAP) and gas analysis were evaluated in all ventilated groups.
Safety parameters were evaluated in all patients who received ≥1 dose of study drug using descriptive statistics.
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