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1 METHODS AND In Bangladesh, we cluster-randomized (1:1) 142 villages of the Matlab Health and Demogr
9 udy selection, we sought systematic reviews, meta-analyses, randomized clinical trials, prospective comparative observati
11 ng of vegetables in both members of the dyad.We conducted a randomized controlled study of 97 mother-infant dyads.
16 plus 5-FU for the field treatment of actinic keratosis in a randomized, double-blind clinical trial involving 131 partici
21 PDR-related complications requiring PPV were prospectively randomized into 1 of 2 treatment groups: Group A received IVB
22 Individual data from 2092 patients with enteric fever randomized into 4 trials in Kathmandu, Nepal, were pooled.
23 duction to Enhance Performance in Dialysis trial, a 6-month randomized, multicenter trial to test whether a simple, perso
27 sions are the same as those found in all four much smaller, randomized, placebo-controlled trials specifically designed t
28 e assigned randomly to the Strong African American Families randomized prevention trial or to a control condition.
29 tic therapy did not reduce 28-day/hospital mortality in the randomized studies (relative risk, 0.93; 95% CI, 0.77-1.13; I
31 or the lung had an emphysematous appearance, patients were randomized to either standard management or interventional pr
33 %) randomized to thrombus aspiration and 262 of 9151 (2.9%) randomized to PCI alone (hazard ratio, 0.84; 95% confidence i
34 reated with primary percutaneous coronary intervention were randomized to prasugrel or ticagrelor with an intended treatm
35 arization following percutaneous coronary intervention were randomized to ranolazine versus placebo.
36 e patients were recruited for this study; 270 patients were randomized to receive eravacycline, and 271 patients were ran
38 allel-group trial, 401 participants aged 6 to 11 years were randomized to receive once-daily tiotropium 5 mug (2 puffs of
41 ar death at 30 days occurred in 221 of 9155 patients (2.4%) randomized to thrombus aspiration and 262 of 9151 (2.9%) rand
42 235 women undergoing PM for Stage 0-III breast cancer were randomized to undergo either standard PM ("no shave", n = 116
46 arly Treatment Program (RAISE-ETP) study, a 34-site cluster-randomized trial, compared NAVIGATE, a coordinated specialty
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