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1 BAAR) in a double-blind, placebo-controlled, crossover study.
2 requency to 12 healthy volunteers in a 2 x 2 crossover study.
3 S were included in a randomised, controlled, crossover study.
4 k, phase 4, randomized, investigator-masked, crossover study.
5 were enrolled in a prospective, randomized, crossover study.
6 separate days in a randomized, double-blind, crossover study.
7 -blind, placebo-controlled, counterbalanced, crossover study.
8 completed this 3-week inpatient, randomized, crossover study.
9 eted this four-centre, double-blind, two-way crossover study.
10 Experiment one is a five-session crossover study.
11 3.7 +/- 3.5 y) were included in a randomized crossover study.
12 Thirty-one surgeons were recruited for a crossover study.
13 rticipated in this randomized, subject-blind crossover study.
14 omized, double-blind, placebo-controlled 3x3 crossover study.
15 corrected, double-blind, placebo-controlled, crossover study.
16 ed, double-blind, placebo-controlled, triple-crossover study.
17 IU) or placebo in a double-blind, randomized crossover study.
18 e studied in this randomized, double-blinded crossover study.
19 in a randomized placebo-controlled three-way crossover study.
20 were enrolled in a 3-period, 7-wk randomized crossover study.
21 ach for 6 weeks in a randomized double-blind crossover study.
22 clonidine, and paroxetine) in a double-blind crossover study.
23 utput in a double-blind, placebo-controlled, crossover study.
24 ) participated in a randomized, double-blind crossover study.
25 icipated in a randomized, placebo-controlled crossover study.
26 andomized, double-blind, placebo-controlled, crossover study.
27 ted in a single-blinded, randomized, 2-phase crossover study.
28 placebo-controlled, randomized, double-blind crossover study.
29 s part of a double-blind, placebo-controlled crossover study.
30 /- 0.6 g/dl) were studied in this randomized crossover study.
31 abetes in a randomized, single-blind, triple-crossover study.
32 -htrA in a double-blind, placebo-controlled, crossover study.
33 (10)]) or air in a double-blind, randomized, crossover study.
34 ram) to placebo in a randomized double-blind crossover study.
35 double blind, placebo-controlled, two-period crossover study.
36 0.5 N saline in a double-blind, randomized, crossover study.
37 hma completed this double-blind, four-period crossover study.
38 consumed on sequential days in a randomized crossover study.
39 sly over 4 hours via pump in this randomized crossover study.
40 obtained through an isotopic double-labeling crossover study.
41 rdia syndrome in a randomized, single-blind, crossover study.
42 a two-drug, placebo-controlled, double-blind crossover study.
43 n; 191.9 +/- 9.9 kcal added) in a randomized crossover study.
44 asked crossover design and 1 with 4 parallel crossover studies.
45 Both were randomized, double-blind, crossover studies.
46 ed in this placebo-controlled, double-blind, crossover study (0.5 mg/kg cortisol or intravenous place
54 andomized, double-blind, placebo-controlled, crossover study, 12 healthy, young males received gonado
58 genous pathway.In a randomized, double-blind crossover study, 16 healthy individuals were supplemente
60 In this single-blind, placebo-controlled crossover study, 16 participants completed two study day
63 randomized, double-blind placebo-controlled crossover study, 19 patients with mild-to-moderate idiop
66 genotype-stratified, double-blind, four-way crossover study, 21 healthy adult subjects were exposed
69 In a multicenter, randomized, open-label, crossover study, 34 blacks with stable CAD receiving ace
72 on instructions; (3) an adequately conducted crossover study; (4) comparison of equivalent doses; (5)
76 a prospective, single-center, single-blind, crossover study, 56 patients with non-ST-elevation acute
78 acebo-controlled, multiple-dose, 2-sequence, crossover study, 64 patients were randomized to receive
81 9% predicted) in a double blind, randomized, crossover study after aerosolization of a single dose of
84 on is proposed in detail and is supported by crossover studies and a number of unambiguous experiment
85 time and with published data and the use of crossover studies and adjustment equations to ensure com
86 d, double-blind, placebo-controlled, two-way crossover studies and an open study in nonallergic subje
87 randomized, placebo-controlled, single-blind crossover study and compared with 12 healthy, nonobese c
88 pated in a double-blind, placebo-controlled, crossover study and inhaled single doses of fluticasone
89 s, including Hammett plots, Eyring analysis, crossover studies, and investigations of the influence o
90 used include multiple-arm trials, randomized crossover studies, and more compromised designs such as
93 ouble-blind, randomised, placebo-controlled, crossover study at 24 sites in North America and Europe.
94 d, double-blind, placebo-controlled 2-period crossover study at 7 neuromuscular referral centers in 4
96 n-label, multicentre, randomised controlled, crossover study between Dec 1, 2012, and Dec 23, 2014, r
97 the meta-analysis was limited to randomized crossover studies, both systolic [1.3 (-0.3, 2.9) mm Hg;
102 med a randomized, double-blind, single-dose, crossover study comparing 0.5 mg/kg MPH with 1.0 mg/kg A
103 s for bleeding in a prospective, randomized, crossover study comparing 6 months of anti-inhibitor coa
104 rticipated in this randomized, double-blind, crossover study comparing a single dose of NO3-rich beet
107 pen-label, expanded safety and acceptability crossover study comparing rectally applied reduced-glyce
109 ans, we performed a randomized, double-blind crossover study comparing the calcium antagonist amlodip
110 double-blind, randomized, placebo-controlled crossover study comparing the effect of the bradykinin B
111 ucted a randomized, multicenter, open-label, crossover study comparing the efficacy and safety of a 1
112 adults underwent a randomized, double-blind, crossover study comparing the vascular response to the 2
113 ion-level exposure time trends can bias case-crossover studies conducted among "first-wave" users of
114 ESIGN, SETTING, AND PARTICIPANTS: Randomized crossover study conducted between January 1 and December
115 zed, controlled, examiner-blind, nine-period crossover study conducted in 72 adult subjects over a 3-
117 y-seven patients on hemodialysis completed a crossover study consisting of two exercise training phas
129 nd pacing backup (AAI-30) in a double-blind, crossover study design, followed by an uncontrolled and
131 ing a prospective, randomized, single-blind, crossover study design, we therefore measured EE and rat
138 double-blind, placebo-controlled, randomized crossover study, disease-free patients at least 1 year p
140 es from 14 mildly hypertensive patients in a crossover study during a high-sodium (HS, 160 mmol/d) di
141 ght adolescents participated in a randomized crossover study during which EAH was measured as intake
143 e-center, double-masked, placebo-controlled, crossover study evaluated the efficacy of 8 weeks of tre
144 a randomized, double-blind, ascending-dose, crossover study evaluating 3 doses of BG9719 in 63 patie
145 double-blind, randomized, placebo-controlled crossover study evaluating the effect of 14 days of XEN-
147 ed, controlled, examiner-masked, five-period crossover study examined plaque removal in 25 subjects f
154 randomized, double-blind, placebo-controlled crossover study in 14 nondiabetic overweight or obese (b
155 a randomized double-blind placebo-controlled crossover study in 16 men, with measurement of liver 11b
156 andomized, double-blind, placebo-controlled, crossover study in 21 PD patients on levodopa but no ago
157 randomized, placebo-controlled, four-period, crossover study in 24 patients with T2D, dipeptidyl pept
158 ducted a randomized, double-blind, three-way crossover study in 27 patients with proteinuric CKD to c
159 ouble-blind, randomised, placebo-controlled, crossover study in a hospital and two infirmaries in the
164 attacks by conducting an internet-based case-crossover study in the United States (in 2003-2010) amon
165 75 mg in a 3-period (12 days each) blinded, crossover study in VE (n = 73; mean: 79 +/- 3 years of a
168 t hoc analysis of the data is functionally a crossover study in which only surviving patients can cro
169 ng men participated in a randomized 3 x 2-wk crossover study in which the following 3 isocaloric diet
170 completed a double-blind, placebo-controlled crossover study in which they received 2 daily subcutane
172 double-blind, randomized, placebo-controlled crossover study included 44 CF patients (aged 7-19 y; 20
174 nalyzed data from 13 double-blind randomized crossover studies including 282 participants (140 health
178 ouble-blind, randomized, placebo-controlled, crossover study, LSD (200 mug) and placebo were administ
182 DESIGN, SETTING, AND PARTICIPANTS: A case-crossover study nested within a prospective cohort study
185 iculate matter (</=2.5 micro m) using a case-crossover study of 1,206 Washington State out-of-hospita
186 e-center, randomized, double-blind, 3-period crossover study of 11 women with IBS (35.50 +/- 12.48 ye
187 new study model, we performed a randomized, crossover study of 12 adult asthmatics who required 800
188 In a single-blinded and placebo-controlled crossover study of 15 healthy participants, we administe
189 EMENTS: In a randomized, placebo-controlled, crossover study of 192 subjects with moderate asthma, we
192 , AND PARTICIPANTS: Prospective, nested case-crossover study of 288 cases of sudden cardiac death wit
193 age, 62 +/- 7 years) completed a, randomized crossover study of 4 weeks of both low (DSR) and normal
194 e, and substrate metabolism in a prospective crossover study of 4-month duration, consisting of four
195 llen Children and Adolescent study is a case-crossover study of 644 children and adolescents (aged 2-
196 dication and serious fall injuries in a case-crossover study of 90 127 Medicare beneficiaries who wer
198 andomized, double-blind, placebo-controlled, crossover study of Adderall in 27 well-characterized adu
202 e performed a randomized, placebo-controlled crossover study of CRF compared with saline injection in
203 ble-blinded, randomized, placebo-controlled, crossover study of DBS targeting the ventral striatum/an
204 A randomized, blinded, placebo-controlled crossover study of either 0.5 mg neostigmine or saline (
206 randomized, double-blind, placebo-controlled crossover study of individuals with self-reported non-ce
207 centre, placebo-controlled, double-blind 2x2 crossover study of ivacaftor treatment was conducted in
208 ble-blind, double-dummy, placebo-controlled, crossover study of objectively assessed nonsmokers (n =
209 nd, placebo-controlled, randomized, 3-period crossover study of OPC-28326 (oral doses of 10 mg or 40
210 conducted a multi-site time-stratified case-crossover study of ozone exposures for approximately 3.7
211 44) was a randomized, double-blind, 2-phase crossover study of prasugrel compared with high-dose clo
213 his was a randomized, double-blind, 12-week, crossover study of rosuvastatin 20 mg versus placebo, fo
214 study was nested within a cluster-randomized crossover study of selective digestive decontamination a
215 e randomized into a double-blind four-period crossover study of sustained-release ranolazine 500, 1,0
217 onducted a double-blind, placebo-controlled, crossover study of the effect of the long-acting beta(2)
218 completed a double-blind, placebo-controlled crossover study of the effects of a single dose of amphe
219 al research sites in an open label, 3-period crossover study of three different daily tenofovir regim
220 al dysfunction were enrolled in a randomized crossover study of transfusing autologous, leukoreduced
221 andomized, double-blind, placebo-controlled, crossover study of two weeks of losartan (50 mg q.d.) on
222 double-blind, randomized, placebo-controlled crossover study of UDCA in 17 clinically stable male pat
223 randomized, placebo-controlled, double-blind crossover study on 10 patients with NYHA class II to III
224 randomized, placebo-controlled, double-blind crossover study on 11 patients with New York Heart Assoc
225 zed, double blind, placebo-controlled, 2-way crossover study on 20 subjects with asthma comparing the
226 tain an intervention group of interest, were crossover studies, or were only published in abstract fo
227 d, double-blind, placebo-controlled, partial-crossover study, participants aged 18 to 65 years with a
229 , SETTING, AND PARTICIPANTS: A single-blind, crossover study, performed in a hypobaric chamber, to as
237 c-dose study was a randomised, double-blind, crossover study that enrolled adults (aged >/=18 years)
241 cohort study and 2 interventional randomized crossover studies to assess: 1) the relationship between
242 lthy volunteers were exposed in a randomized crossover study to 0.3 ppm ozone and clean air for 2 hr
243 lled in a double-blinded, placebo-controlled crossover study to assess the effect of 1200 mg of gamma
244 were enrolled in a bicentric intraindividual crossover study to compare lesion enhancement with doses
245 lind placebo-controlled randomized three-way crossover study to compare the hemodynamic effects of 7
247 blind, randomized, placebo-controlled, 2-way crossover study to determine the reversal effect of desc
250 ouble-blind, randomized, placebo-controlled, crossover study to follow spirometry, quality of life qu
251 -period, double-blind, balanced Latin square crossover study to receive placebo, and ranolazine 500,
254 andomized, double-blind, placebo-controlled, crossover study using functional magnetic resonance imag
258 d, double-blind, placebo-controlled, two-way crossover study was conducted in 35 male subjects allerg
260 andomized, double-blind, placebo-controlled, crossover study was conducted in 80 patients with CAD, c
261 le-blind, placebo-controlled, within-subject crossover study was conducted in healthy adults (n=17).
262 , double-blind, placebo-controlled, 2-period crossover study was conducted with the Vienna Challenge
264 andomized, double-blind, placebo-controlled, crossover study was designed to determine the safety and
270 d, double-blind, placebo-controlled, two-way crossover study was performed in 22 steroid-naive mild-t
274 se of this double-blind, placebo-controlled, crossover study was to determine age-related differences
276 rpose of this sham-controlled, double-blind, crossover study was to identify the neural circuitry tha
286 Here, in a 6-month double-blind alternating crossover study, we show that bilateral deep brain elect
289 andomized, placebo-controlled, double-blind, crossover studies were performed for 1 month on patients
295 In this prospective, randomized, open-label crossover study with masked outcome assessments, stable
296 performed a randomized, placebo-controlled, crossover study with prednisolone (40 mg daily) or place
297 randomized, double-blind, placebo-controlled crossover study with single-dose intranasal oxytocin (24
298 healthy men were studied in a single-blind, crossover study with two randomized visits (one with 40
299 ere studied in a randomized, double-blinded, crossover study, with 2-h intravenous administration of
300 Furthermore, in a double-blind, randomized, crossover study, xylitol sprayed for 4 days into each no
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