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1 obtained through an isotopic double-labeling crossover study.
2 rdia syndrome in a randomized, single-blind, crossover study.
3 a two-drug, placebo-controlled, double-blind crossover study.
4 n; 191.9 +/- 9.9 kcal added) in a randomized crossover study.
5 BAAR) in a double-blind, placebo-controlled, crossover study.
6 requency to 12 healthy volunteers in a 2 x 2 crossover study.
7 S were included in a randomised, controlled, crossover study.
8 k, phase 4, randomized, investigator-masked, crossover study.
9 were enrolled in a prospective, randomized, crossover study.
10 separate days in a randomized, double-blind, crossover study.
11 -blind, placebo-controlled, counterbalanced, crossover study.
12 completed this 3-week inpatient, randomized, crossover study.
13 eted this four-centre, double-blind, two-way crossover study.
14 Experiment one is a five-session crossover study.
15 a single-blind, randomized, case-controlled crossover study.
16 3.7 +/- 3.5 y) were included in a randomized crossover study.
17 randomized, double-blind, placebo-controlled crossover study.
18 Thirty-one surgeons were recruited for a crossover study.
19 rticipated in this randomized, subject-blind crossover study.
20 omized, double-blind, placebo-controlled 3x3 crossover study.
21 ed, double-blind, placebo-controlled, triple-crossover study.
22 e studied in this randomized, double-blinded crossover study.
23 in a randomized placebo-controlled three-way crossover study.
24 were enrolled in a 3-period, 7-wk randomized crossover study.
25 andomized, double-blind, placebo-controlled, crossover study.
26 ach for 6 weeks in a randomized double-blind crossover study.
27 clonidine, and paroxetine) in a double-blind crossover study.
28 utput in a double-blind, placebo-controlled, crossover study.
29 ) participated in a randomized, double-blind crossover study.
30 icipated in a randomized, placebo-controlled crossover study.
31 andomized, double-blind, placebo-controlled, crossover study.
32 ted in a single-blinded, randomized, 2-phase crossover study.
33 placebo-controlled, randomized, double-blind crossover study.
34 s part of a double-blind, placebo-controlled crossover study.
35 pants in a double-blind, placebo-controlled, crossover study.
36 9 y) completed this randomized, controlled, crossover study.
37 The study design was a double-blind crossover study.
38 corrected, double-blind, placebo-controlled, crossover study.
39 IU) or placebo in a double-blind, randomized crossover study.
40 abetes in a randomized, single-blind, triple-crossover study.
41 consumed on sequential days in a randomized crossover study.
42 sly over 4 hours via pump in this randomized crossover study.
43 Both were randomized, double-blind, crossover studies.
44 asked crossover design and 1 with 4 parallel crossover studies.
51 andomized, double-blind, placebo-controlled, crossover study, 12 healthy, young males received gonado
53 ts.Methods: In this randomized, double-blind crossover study, 14 allergen-sensitized participants (9
56 ngle phthalate, DBP.Methods: In a randomized crossover study, 16 allergen-sensitized participants wer
57 genous pathway.In a randomized, double-blind crossover study, 16 healthy individuals were supplemente
59 In this single-blind, placebo-controlled crossover study, 16 participants completed two study day
62 randomized, double-blind placebo-controlled crossover study, 19 patients with mild-to-moderate idiop
65 genotype-stratified, double-blind, four-way crossover study, 21 healthy adult subjects were exposed
68 In a multicenter, randomized, open-label, crossover study, 34 blacks with stable CAD receiving ace
71 on instructions; (3) an adequately conducted crossover study; (4) comparison of equivalent doses; (5)
75 a prospective, single-center, single-blind, crossover study, 56 patients with non-ST-elevation acute
76 acebo-controlled, multiple-dose, 2-sequence, crossover study, 64 patients were randomized to receive
82 on is proposed in detail and is supported by crossover studies and a number of unambiguous experiment
83 time and with published data and the use of crossover studies and adjustment equations to ensure com
84 randomized, placebo-controlled, single-blind crossover study and compared with 12 healthy, nonobese c
85 pated in a double-blind, placebo-controlled, crossover study and inhaled single doses of fluticasone
86 s, including Hammett plots, Eyring analysis, crossover studies, and investigations of the influence o
87 led in a double-blinded, placebo-controlled, crossover study, and peripheral blood was collected at b
90 ouble-blind, randomised, placebo-controlled, crossover study at 24 sites in North America and Europe.
91 d, double-blind, placebo-controlled 2-period crossover study at 7 neuromuscular referral centers in 4
94 n-label, multicentre, randomised controlled, crossover study between Dec 1, 2012, and Dec 23, 2014, r
95 the meta-analysis was limited to randomized crossover studies, both systolic [1.3 (-0.3, 2.9) mm Hg;
98 med a randomized, double-blind, single-dose, crossover study comparing 0.5 mg/kg MPH with 1.0 mg/kg A
99 s for bleeding in a prospective, randomized, crossover study comparing 6 months of anti-inhibitor coa
100 rticipated in this randomized, double-blind, crossover study comparing a single dose of NO3-rich beet
101 zed, single-blind, placebo-controlled, 2-way crossover study comparing cough responses to inhaled cap
103 pen-label, expanded safety and acceptability crossover study comparing rectally applied reduced-glyce
105 double-blind, randomized, placebo-controlled crossover study comparing the effect of the bradykinin B
106 ucted a randomized, multicenter, open-label, crossover study comparing the efficacy and safety of a 1
108 adults underwent a randomized, double-blind, crossover study comparing the vascular response to the 2
109 a double-blind, randomized, counterbalanced, crossover study comprising 23 healthy human participants
110 ion-level exposure time trends can bias case-crossover studies conducted among "first-wave" users of
111 ESIGN, SETTING, AND PARTICIPANTS: Randomized crossover study conducted between January 1 and December
112 zed, controlled, examiner-blind, nine-period crossover study conducted in 72 adult subjects over a 3-
114 y-seven patients on hemodialysis completed a crossover study consisting of two exercise training phas
125 ing a prospective, randomized, single-blind, crossover study design, we therefore measured EE and rat
126 ion in a double-blinded, placebo-controlled, crossover study design, where paired skeletal muscle tis
132 double-blind, placebo-controlled, randomized crossover study, disease-free patients at least 1 year p
134 es from 14 mildly hypertensive patients in a crossover study during a high-sodium (HS, 160 mmol/d) di
135 ght adolescents participated in a randomized crossover study during which EAH was measured as intake
137 s and Methods This prospective observational crossover study enrolled 42 patients undergoing lower li
138 e-center, double-masked, placebo-controlled, crossover study evaluated the efficacy of 8 weeks of tre
139 stries, we conducted a population-based case-crossover study evaluating the association between switc
140 double-blind, randomized, placebo-controlled crossover study evaluating the effect of 14 days of XEN-
142 andomized, placebo-controlled, double-blind, crossover study, evaluating performance in four value-ba
143 ed, controlled, examiner-masked, five-period crossover study examined plaque removal in 25 subjects f
148 In this double-blind, randomized, two-period crossover study, gadolinium-enhanced MRI and phase-resol
151 randomized, double-blind, placebo-controlled crossover study in 14 nondiabetic overweight or obese (b
152 a randomized double-blind placebo-controlled crossover study in 16 men, with measurement of liver 11b
153 andomized, double-blind, placebo-controlled, crossover study in 21 PD patients on levodopa but no ago
154 randomized, placebo-controlled, four-period, crossover study in 24 patients with T2D, dipeptidyl pept
155 ducted a randomized, double-blind, three-way crossover study in 27 patients with proteinuric CKD to c
156 ouble-blind, randomised, placebo-controlled, crossover study in a hospital and two infirmaries in the
162 attacks by conducting an internet-based case-crossover study in the United States (in 2003-2010) amon
163 75 mg in a 3-period (12 days each) blinded, crossover study in VE (n = 73; mean: 79 +/- 3 years of a
166 t hoc analysis of the data is functionally a crossover study in which only surviving patients can cro
167 ng men participated in a randomized 3 x 2-wk crossover study in which the following 3 isocaloric diet
168 completed a double-blind, placebo-controlled crossover study in which they received 2 daily subcutane
170 double-blind, randomized, placebo-controlled crossover study included 44 CF patients (aged 7-19 y; 20
172 nalyzed data from 13 double-blind randomized crossover studies including 282 participants (140 health
173 ed for a double-blinded, placebo-controlled, crossover study including 6 experimental days in a rando
177 a double-blind, randomized, sham-controlled, crossover study involving two sessions of neurofeedback
178 ouble-blind, randomized, placebo-controlled, crossover study, LSD (200 mug) and placebo were administ
182 ubstudy of UChoose, an open-label randomized crossover study (NCT02404038), comparing acceptability a
183 DESIGN, SETTING, AND PARTICIPANTS: A case-crossover study nested within a prospective cohort study
186 iculate matter (</=2.5 micro m) using a case-crossover study of 1,206 Washington State out-of-hospita
187 e-center, randomized, double-blind, 3-period crossover study of 11 women with IBS (35.50 +/- 12.48 ye
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
191 , AND PARTICIPANTS: Prospective, nested case-crossover study of 288 cases of sudden cardiac death wit
192 age, 62 +/- 7 years) completed a, randomized crossover study of 4 weeks of both low (DSR) and normal
193 e, and substrate metabolism in a prospective crossover study of 4-month duration, consisting of four
194 llen Children and Adolescent study is a case-crossover study of 644 children and adolescents (aged 2-
195 dication and serious fall injuries in a case-crossover study of 90 127 Medicare beneficiaries who wer
198 d inpatient hospital admissions in this case-crossover study of adult patients visiting a large urban
201 e performed a randomized, placebo-controlled crossover study of CRF compared with saline injection in
202 ble-blinded, randomized, placebo-controlled, crossover study of DBS targeting the ventral striatum/an
203 A randomized, blinded, placebo-controlled crossover study of either 0.5 mg neostigmine or saline (
204 e completed a randomized, placebo-controlled crossover study of empagliflozin 10 mg daily versus plac
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 andomized, double-blind, placebo-controlled, crossover study of one dose of 50 mg of naltrexone, or p
210 nd, placebo-controlled, randomized, 3-period crossover study of OPC-28326 (oral doses of 10 mg or 40
211 conducted a multi-site time-stratified case-crossover study of ozone exposures for approximately 3.7
212 44) was a randomized, double-blind, 2-phase crossover study of prasugrel compared with high-dose clo
214 his was a randomized, double-blind, 12-week, crossover study of rosuvastatin 20 mg versus placebo, fo
215 study was nested within a cluster-randomized crossover study of selective digestive decontamination a
216 e randomized into a double-blind four-period crossover study of sustained-release ranolazine 500, 1,0
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 double-blind, randomized, placebo-controlled crossover study of UDCA in 17 clinically stable male pat
222 randomized, placebo-controlled, double-blind crossover study on 11 patients with New York Heart Assoc
223 zed, double blind, placebo-controlled, 2-way crossover study on 20 subjects with asthma comparing the
224 tain an intervention group of interest, were crossover studies, or were only published in abstract fo
225 d, double-blind, placebo-controlled, partial-crossover study, participants aged 18 to 65 years with a
226 randomized, double-blind, placebo-controlled crossover study, patients >=1 y after ES and matched con
228 , SETTING, AND PARTICIPANTS: A single-blind, crossover study, performed in a hypobaric chamber, to as
234 c-dose study was a randomised, double-blind, crossover study that enrolled adults (aged >/=18 years)
239 cohort study and 2 interventional randomized crossover studies to assess: 1) the relationship between
240 lthy volunteers were exposed in a randomized crossover study to 0.3 ppm ozone and clean air for 2 hr
241 lled in a double-blinded, placebo-controlled crossover study to assess the effect of 1200 mg of gamma
242 were enrolled in a bicentric intraindividual crossover study to compare lesion enhancement with doses
243 lind placebo-controlled randomized three-way crossover study to compare the hemodynamic effects of 7
245 blind, randomized, placebo-controlled, 2-way crossover study to determine the reversal effect of desc
247 andomized, double-blind, placebo-controlled, crossover study to examine dose-related effects of AV-10
249 -period, double-blind, balanced Latin square crossover study to receive placebo, and ranolazine 500,
252 andomized, double-blind, placebo-controlled, crossover study using functional magnetic resonance imag
257 d, double-blind, placebo-controlled, two-way crossover study was conducted in 35 male subjects allerg
259 andomized, double-blind, placebo-controlled, crossover study was conducted in 80 patients with CAD, c
260 le-blind, placebo-controlled, within-subject crossover study was conducted in healthy adults (n=17).
261 , 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
278 randomised controlled non-blinded eight-arm crossover study was used to assess plasma nicotine pharm
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
291 andomized, placebo-controlled, double-blind, crossover study were consistent with an inverted U-shape
296 In this prospective, randomized, open-label crossover study with masked outcome assessments, stable
297 performed a randomized, placebo-controlled, crossover study with prednisolone (40 mg daily) or place
298 randomized, double-blind, placebo-controlled crossover study with single-dose intranasal oxytocin (24
299 healthy men were studied in a single-blind, crossover study with two randomized visits (one with 40
300 ere studied in a randomized, double-blinded, crossover study, with 2-h intravenous administration of