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    Plasma tHcy levels were compared in the CC and TT genotypes in the different groups to investigate the effect of the mutant allele (T). There was no significant difference regarding the tHcy between the CC and TT genotypes in Gp1 or Gp2. The CC genotype had a plasma tHcy of 18.74 ± 11.26 and 38.55 ± 22.63 μmol/L, while the TT genotype had a plasma tHcy of 12.2 ± 4.58 and 36.25 ± 8.96 in Gp1 and Gp2 respectively. On the other hand, in the patients group the CC genotype had an even significantly higher plasma tHcy when compared with the TT genotype (P<0.05). The CC and the TT genotypes had plasma tHcy of 51.09 ± 28.37 and 22.33 ± 6.71 respectively. (Figure 3). For the purpose of this report Lurasidone canada data were abstracted by the SHARE program data manager who was not blinded to the study question. The data were then transported from Microsoft Access for Windows (Microsoft, Redmond, WA) into the Stata 12.1 (StataCorp, College Station, TX) statistical package program for the statistical analysis. Subjects who could not be geocoded due to incomplete address information were excluded from the analysis. The rate of BCPR provision and survival to hospital discharge in each group according to neighborhood main ethnicity were compared using the χ2 test. A multivariate logistic regression analysis was performed to determine the association between BCPR provision and survival to hospital discharge with neighborhood main ethnicity while adjusting for confounders: age, sex, if arrests were witnessed or not, location of arrest, call to EMS arrival time, initially monitored rhythm (for survival to discharge), and neighborhood poverty rate. The goodness-of-fit for regression model was assessed by Hosmer-Lemeshow test.. In our single center Lurasidone canada we designed a retrospective analysis between 2008 and 2011 to compare the initial experiences in fluoroscopy-guided approaches for PVI regarding the PD and FT using I) the HDMM with irrigated-tip RF for segmental ostial ablation, II) the single device RF and mapping technique of the HDMA, and III) the single device cryothermal energy of the Arctic Front® cryoballoon. For PVI, we started recording PD and FT with the transfemoral puncture and stopped recording the time when disconnection of all PVs was achieved. No intraprocedural imaging except for fluoroscopy was used in this study. The primary endpoints were FT and PD, the secondary endpoint was procedural safety and efficacy in short- and long-term follow-up..

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