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1                                                             There was no apparent interaction between Px and Iso treatmen
2                                                             There was no association between liver stiffness and any pati
3                                                   Moreover, there was no association between unit policies and prolongati
4                                                             There was no association with ART initiation in the hospital
5                                                             There was no association with cognition, language or behaviou
6  active surveillance was not statistically significant, and there was no association with upgrading in surveillance biops
7 t at KT and showed the greatest increase in height, whereas there was no catch-up growth in children transplanted >12.
8                                                             There was no change in IGF-1 level from before to after surge
9          When additional organisms were identified by mNGS, there was no change in management in the majority of cases.
10                                                    However, there was no consensus on the relevance of REA, including how
11                                                             There was no correlation between activity and PROMs, but a st
12                                                             There was no difference between the two interventions on the
13 mice was decreased; however, mice were not neutropenic, and there was no difference in absolute blood neutrophils between
14                                                             There was no difference in adverse events between randomised
15                                                             There was no difference in insulin or insulin resistance betw
16                                                  Similarly, there was no difference in patient survival at 1 (94% versus
17                                                             There was no difference in risk of 90-day mortality between b
18 ean titers than mothers of KSHV-positive children; however, there was no difference in the presence of neutralizing antib
19                                                             There was no discordance when all the echocardiographic param
20                                                  Similarly, there was no dose-dependent relationship between PPS exposure
21                                       For primary outcomes, there was no effect of any UBL intervention compared to contr
22                                                             There was no evidence for associations of physical activity w
23                                                             There was no evidence for increased risks of prostate or colo
24                         In the intention-to-treat analysis, there was no evidence of a difference in the proportion of pa
25                                                             There was no evidence of interaction between MRD status and c
26                                                             There was no evidence of large reductions in SFA, but we are
27                                                             There was no evidence that concussion or vision symptom traje
28  earlier and had no medical history of note; in particular, there was no history of cancer or predisposing factors for ch
29 io, 1.15; 95% confidence interval, 1.06, 1.24); conversely, there was no increased risk in women with dental caries and t
30                                                             There was no masking in this open-label trial.
31 25 h shifts (predicted probability 99.4% vs 78.8%), whereas there was no relevant difference between the beginning and en
32                         In multivariable adjusted analyses, there was no significant association between baseline eGFR <6
33                                                             There was no significant association between donor MDRO and e
34                                                             There was no significant association between the duration of
35                                                             There was no significant change in LOS or discharge home rate
36 re significantly lower in IUGR than control foetuses, while there was no significant difference among IUGR groups.
37                                                             There was no significant difference between the erythropoieti
38 iated with improvement of these energetic changes such that there was no significant difference in comparison with contro
39 l including the 47 participants completing >=1 diet period, there was no significant difference in DAS28-ESR between the
40                                                             There was no significant difference in patients' satisfaction
41 cute health care use and modestly lower symptom burden, but there was no significant difference in quality of life.
42                                                             There was no significant difference in rate of death by suici
43                                                         But there was no significant difference in the expression of IL-1
44 ophrenia with large effect sizes (Cohen's d = 0.8-0.9), but there was no significant difference in the hippocampus.
45            Within the limitations of this interim analysis, there was no significant difference in treatment time, satisf
46                                                  Similarly, there was no significant difference within different types of
47                                                             There was no statistically significant difference in readmiss
48                                                             There was no statistically significant difference in the inci
49 all-cause mortality (HR, 0.83 [95% CI, 0.75-0.92]), whereas there was no statistically significant mortality reduction wi
50                                                             There was no toxic mortality.