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We assessed the data in several ways.
We assessed the data according to subgroups of OHCA and IHCA, but conversely, the sample size is rather weakened.
In the third analysis, we assessed the data quality of the recorded patient-related outcome scores (KOOS and Tegner scores).
In this, study, we assessed the data quality, reliability, validity and responsiveness of the Norwegian version of the EC-17.
To detect possible genotyping error, for family data, we assessed the data for Mendelian consistencies by the program PEDCHECK [ 54], with no non-Mendelian inconsistencies detected.
We assessed the data from patient records to ascertain if first or second line drugs were prescribed to children diagnosed with these diseases.
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In our study, we assess the data reconstruction error using the mean squared error normalized by the data size and by the difference between the maximum and minimum value in the data.
We then assessed the data for completeness, consistency and accuracy.
We initially assessed the data in a gender-dependent manner for all of the study participants (HIV-positive HAART and HAART-naïve).
With the endpoint in 2005, we assessed the clinical data by chart analysis blind to genotyping (Table 1).
We assessed the extracted data about the efficacy and safety to synthetically evaluate the treatment of included vaptans for cirrhosis patients with ascites.
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