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Demographic, clinical and biological data were compared between patients with and without decision of LST limitation.
Clinical and biological data were compared between thrombopenic and non thrombopenic group.
Finally, two subgroups were defined according to the duration of MV (≤ or >15 days) and all of their clinical and biological data were compared to seek for significant predictors of prolonged MV.
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Biological and histological data were compared using non-parametric tests.
Biological and treatment data were compared between baseline and 6 months after starting HD and CCF.
Their epidemiological, clinical, biological, radiological, evolutive, therapeutic and obstetrical data were compared with patients without cerebral lesions through a descriptive, univariate and multivariate analysis.
To strengthen the process of identifying target genes, gene expression data were compared to other biological parameters, including DNA adduct formation, determined by P-postlabelling analysis, and cell cycle progression, measured by FACS analysis.
Averaged data were compared using t-test.
Cytological and physiological data were compared.
Furthermore, (4) a small biological example of plant phylogeny is presented in which reconstructions that either base on sequence-only or sequence-structure data are compared.
So data are compared to this state.
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