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1 ognitively normal individuals, neurodegeneration biomarkers did not differ between Abeta-N+ and Abeta+N+ cases.
2 mong alemtuzumab recipients than among rATG recipients, but did not differ between basiliximab and rATG recipients.
3 jective pleasantness ratings and skin conductance responses did not differ between behavioural variant frontotemporal dem
5 Incidence of treatment-emergent adverse events did not differ between extended-pulsed fidaxomicin (121 [67%]
7 e are indications that, before flooding, relative head size did not differ between future island and future mainland site
13 were percutaneous coronary interventions (94.2%), and this did not differ between groups (P=0.274).
15 The rate of stent thrombosis, a safety indicator, did not differ between groups and was low in both treatment g
21 were lower in elevated CO2 plots than in ambient plots, but did not differ between heat treatments.
22 hysical activity, 24-h glycemia, and 24-h insulin secretion did not differ between intervention days.
23 comes; (2) averaged between each patient's 2 eyes, outcomes did not differ between ISBCS and DSBCS patients.
24 expression levels of AROM, estrogen and androgen receptors did not differ between males and females and were not sex-spe
30 B-6, and vitamin D (data collected from 2009 through 2010) did not differ between participants with gluten-related condi
32 ctors though was due to starvation, and final removal rates did not differ between reactors inoculated with immobilized a
33 ling to participate in a biobank; willingness and attitudes did not differ between respondents in the three scenarios.
39 ions performed by nonexperts (primarily residents, n = 290) did not differ between the groups (84.4% with video laryngosc
40 s adverse reactions were recorded and other safety measures did not differ between the groups, after allowing for missing
43 uximab group and 593 in the control group, overall survival did not differ between the treatment groups in the entire stu
44 edian overall survival in the intention-to-treat population did not differ between the treatment groups: 7.7 months (95%
45 r, changes in cardiac troponin T levels during the infusion did not differ between the two groups in the 55% of patients
46 verse events, mostly mild self-limited joint and back pain, did not differ between the yoga and PT groups.
47 oportion of patients alive and progression free at 24 weeks did not differ between those who received doxorubicin versus
48 CI 0.36-0.86; p=0.0071), although progression-free survival did not differ between treatment groups in this subgroup (0.6
49 The overall rate of serious adverse events did not differ between treatment groups, although some specif
50 stochemistry showed that HOXB13 gene and protein expression did not differ between tumour samples from variant and wild-t
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