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3 of pregnancy by using a subset of cord blood samples from a randomized, double-blind, placebo-controlled clinical trial (
5 with Preserved Ejection Fraction), which is a multicenter, randomized, double-blind, placebo-controlled cross-over study
7 men underwent functional magnetic resonance imaging using a randomized, double-blind, placebo-controlled crossover study
10 We conducted an international, prospective, multicenter, randomized, double-blind, placebo-controlled, dose-ranging, p
11 depressive disorder (MDD) was examined in a 3-site, 8-week, randomized, double-blind, placebo-controlled, fixed-dose tria
14 samples obtained from 19 children before, during, and after randomized, double-blind, placebo-controlled oral challenges
15 ated patients with asthma from 3 phase IIB and 4 phase IIIA randomized, double-blind, placebo-controlled, parallel group,
17 Phase 3 Trial to Study Efficacy in Nonmetastatic RCC) was a randomized, double-blind, placebo-controlled phase 3 clinical
20 on 51: an open label study including 12 patients; a phase 3 randomized, double blind, placebo controlled study involving
23 is an investigator-initiated, multicenter, prospective, 1:1 randomized, double-blind, placebo-controlled study.
24 We yoked anatomical brain magnetic resonance imaging to a randomized, double-blind, placebo-controlled trial (RCT) of a
30 Kidney Disease Antidepressant Sertraline Trial (CAST) was a randomized, double-blind, placebo-controlled trial involving
38 The Physicians' Health Study II was a randomized, double-blind, placebo-controlled trial testing mu
39 The Vitamin D Assessment Study is a randomized, double-blind, placebo-controlled trial that recru
42 no medical history or signs of asthma, were included in the randomized, double-blind, placebo-controlled trial, comprisin
46 use Of Hydroxyurea in an African Region with Malaria) was a randomized, double-blinded, placebo-controlled trial conducte
47 Data were pooled from two phase III, randomized, double-blind, placebo-controlled trials of IFN-ga
49 rsistency Of Response After Long-Term Therapy (XPORT) was a randomized, double-blind, placebo-controlled withdrawal study
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