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Objective chronotype identification (e.g., based on actigraphs/smartphones) has potential utility, but to date, chronotype has mostly been assessed by questionnaires.
So far, the functional significance of these brain responses has mostly been assessed by analyzing bivariate relationships between noxious stimuli and brain activity, or between brain activity and pain perception.
To minimize bias, behavioral assays have mostly been assessed by two experimenters in a blinded fashion.
Thus, the efficiency of plasma cytokines removal has mostly been assessed during CRRT.
To date, the everyday practical capabilities of dementia patients have mostly been assessed by others (e.g., family members or nurses).
Despite the widespread use of JE vaccines and the circulation of heterologous genotypes, vaccine-induced neutralization capacity has mostly been assessed solely against the strain homologous to the vaccine strain [ 10– 10].
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Their effectiveness, however, has been assessed mostly in controlled experimental environments rather than in complex natural conditions.
However, fatigue has been assessed mostly by single items in general symptom checklists.
Changes in fruit ripening have been assessed mostly using transcriptomics [ 62, 77, 95].
The accuracy of innovative SNP genotyping technologies has been assessed mostly through the development of assays suitable for analysing variations in the human genome.
The duration of MRSA and VRE colonization has previously been assessed in mostly small studies.
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