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As far as TNF- α was concerned, statistically significant difference between groups was identified (PAD group = 1.14 ± 0.45; non-PAD group = 1.04 ± 0.45; t-test: statistics = 2.105, P-value = 0.0360), but this difference has no clinical significance since the values in both groups are within normal range (0.550 2.816 pg/mL).
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Innovative imaging techniques are needed to identify PAD subjects at the highest vascular risk.
Although reduced lower extremity performance was reported to be a prognostic marker for mortality, little is known about useful biomarkers for identifying PAD patients at high risk.
Together, these data provide the rationale for defining stratification criteria for a severity score to estimate reliably the achievable benefit in routine practice and/or identify PAD subjects at the highest risk of amputation/vascular death.
The abnormal cut-off value of 1.2 pg/mL (0.016 ng/mL) for log10 [hsTnT] in the present study indicates that it is possible that troponin leakage detected by both high-sensitivity cardiac TnT and conventional TnT could identify PAD patients at high risk.
No genotype differences in terms of SNP+45 or SNP+276 were identified between PAD and non-PAD groups (Table 2).
To evaluate the feasibility of implementing a pharmacist-initiated peripheral arterial disease (PAD) screening program in the community setting and to determine the ability of this screening to increase the number of patients identified with PAD.
All objects that are lying on the table are identified by padding of the closed contours in the table template, calculated through color segmentation, and then subtracting the template before the padding.
Separation of the fat pad was identified when the fat pad was physically pushed away from the femur or tibia (Fig. 3).
Since fibrin deimination occurs in the rheumatoid synovial tissue, we undertook to identify which PAD types are expressed in the tissue.
Regardless of the specific reason for the high selectivity of GSK199, our studies highlight the potential of exploiting the structural transitions that occur upon calcium binding to identify allosteric PAD inhibitors.
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