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In follow-up controls.
Follow-up controls were planned at 30 and 60 days.
Clinical and roentgenographic follow-up controls were performed at 1, 3, 6, and 18 months.
Employing a nested case-control study design, the CD14 C -260)T polymorphism was evaluated among 387 study partiC -260s who developed MI (cases) and among an equal number of age- and smoking-maTched study polymorphism was revaluatedree of vamongar diseases during follow-up (controls).
Follow-up controls were performed every 2 months thereafter.
Patients received the same protocol of adjuvant chemoradiation and they underwent fixed follow-up controls.
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A pretest-posttest follow-up control group design with random assignment was used.
The scheme is mainly composed of a robust tracking algorithm and a six-DOF follow-up control law.
This was a prospective longitudinal crossover study with an average 10.5-month follow-up, controlled through the use of a placebo device.
On the follow-up control four patients reported that they had been forced to change their preoperative job, whereas 12 out of 22 were able to practice sport.
Also, for both screening examinations, an inconclusive test in the actual year may make it necessary for a follow-up control screening examination in the next year.
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