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1 Further controlled studies should evaluate its efficacy and safety.
2 oparticle biodistribution is essential for evaluating their efficacy and safety.
3 l treatments, and on the consistency of evidence, degree of efficacy, and safety.
6 pproval from regulatory agencies, and for this reason their efficacy and safety are rarely proven.
7 her rigorous clinical studies are needed to determine their efficacy and safety, as well as the appropriate patient candi
8 molar affinity CAR T cells demonstrated superior anti-tumor efficacy and safety compared to their nanomolar counterparts.
10 cholesterol concentrations achieved at 4 weeks and clinical efficacy and safety in the FOURIER trial of evolocumab, a mon
15 lind, randomized, placebo-controlled trial, we assessed the efficacy and safety of adalimumab in children and adolescents
16 The objective of this study was to investigate the efficacy and safety of adjunctive lanicemine (NMDA channel bl
17 It was the aim of this study to evaluate feasibility, efficacy and safety of ADVOS in the first 14 patients ever tr
18 ompositional differences among extracts that may affect the efficacy and safety of allergen immunotherapy.
19 e authors performed an updated meta-analysis evaluating the efficacy and safety of CAS versus CEA, given recently publish
30 to synthesize, appraise, and present all SR evidence on the efficacy and safety of inhaled short-acting bronchodilators t
31 This preplanned analysis assessed the efficacy and safety of IRd vs placebo-Rd according to cytogen
32 lacebo-controlled, phase 3, crossover trial to evaluate the efficacy and safety of ivacaftor alone or in combination with
34 omized, placebo-controlled, phase 3 trial, we evaluated the efficacy and safety of levosimendan in patients with a left v
36 se II/III randomized, double-blind trial designed to assess efficacy and safety of nintedanib plus chemotherapy as first-
37 dose-escalation, phase I CheckMate 016 study evaluated the efficacy and safety of nivolumab plus ipilimumab in combinati
38 Dietary assessment and modelling are required to monitor efficacy and safety of ongoing strategic vitamin D fortificat
40 This phase 2 study was designed to test the efficacy and safety of pembrolizumab, a humanized PD-1-blocki
41 To evaluate the long-term (24-month) efficacy and safety of ranibizumab 0.5 mg administered pro re
46 ts from recent studies strengthen the evidence base for the efficacy and safety of sublingual immunotherapy in patients w
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