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2 at baseline and follow-up were reduced using factor analyses, and factors (both at baseline and at th
4 eas that provide fundamental tools for human factors analyses are summarized, and several current app
5 se the mobility of B3 based on anisotropic B-factor analyses at ultrahigh resolution, consistent with
7 data sets for different locations and times; factor analyses for heat vulnerability are more robust t
8 lations in one of the first large-scale risk factor analyses for new herd breakdowns to combine data
9 tal disorders were analyzed via confirmatory factor analyses for the entire National Comorbidity Surv
10 iatric screening tools to perform prognostic factor analyses for treatment safety during the first 4
16 e was replicated with additional exploratory factor analyses in the same sample at 4-month and 8-mont
23 report presents the results of confirmatory factor analyses of patterns of comorbidity among 10 comm
29 ontrols with gene function and transcription factor analyses potentially related to elevated inflamma
36 ses and 2,410 controls were grouped by using factor analyses to describe various aspects of lifestyle
37 w-up by using risk-stratified and prognostic factor analyses to determine if treatment outcomes diffe
38 s supported by multiparameter solvent effect factor analyses utilizing the KOMPH2 equation which, in
39 asize the postengraftment timing of IA; risk factor analyses verify previously recognized risk factor
46 trol for demographic and cardiovascular risk factors; analyses were stratified by the presence of cor
47 nstruct validity was assessed in exploratory factor analyses which supported a refinement in the conc
48 e has good structural validity (confirmatory factor analyses with Comparative Fit Index > 0.90 and Ro
50 ensionality of the items was evaluated using factor analyses with results suggesting 3 factors in fai
51 ensionality of the items was evaluated using factor analyses, with results suggesting three factors i
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