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1 3% less starch digested at 90 min, P < 0.05, paired t test).
2 d point (core cancer length) was calculated (paired t test).
3 29 [88] mum; P = .01, determined by use of a paired t test).
4 pulses s(-1)) (P < 0.05 for each comparison; paired t test).
5 ly higher than mean serum levels (P </=0.02; paired t test).
6 gnificantly enhanced with OSEM-3D (P < .001, paired t test).
7 BA(A) currents by 70+/-8% (n=8, P< or =0.005 paired t test).
8 left ventricular (LV) surface area (P < .05, paired t test).
9 ent; 4, very poor) for six colonic segments (paired t test).
10 +/- 2.0 micromol/kg body wt per d; P < 0.05, paired t test).
11 in early group (0.56 cm3 +/- 0.39; P =.004, paired t test).
12 mice was significantly increased (P = 0.037, paired t test).
13 es derived from the mothers (P < 0.0001 by a paired t test).
14 d P = 0.02, respectively, as determined by a paired t test).
15 unit accuracy in seven regions of interest (paired t test).
16 l normalization (12.7% vs. 6.2%, P < 0.0001, paired t-test).
17 o eyes (P = 0.69 and P = 0.43, respectively, paired t-test).
18 -R(-/-): P < 0.01; alpha2A-R(-/-): P < 0.05, paired t-test).
19 microm vs. 506.4 +/- 31.8 microm, P = 0.005, paired t-test).
20 (P = 0.0016 and P = 0.0022, respectively, by paired t-test).
21 occipital lobe seen in controls (p < 0.001, paired t-test).
22 se agreement with a confidence level of 95% (paired t-test).
23 th reference values at 95% confidence level (paired t-test).
24 -0.26) significantly decreased (P < .005 in paired t tests).
25 nt in dimensional measurements was compared (paired t tests).
26 e compared with controls (p < 0.05 for each, paired t-tests).
27 oelectron volts) and phantom size by using a paired t test.
28 es of CL and IOL groups were compared with a paired t test.
29 Group comparisons were analyzed with a paired t test.
30 Significance testing was done with the paired t test.
31 Statistical analysis was performed with the paired t test.
32 isons were analyzed with the Mann-Whitney or paired t test.
33 en baseline and week 8 were calculated using paired t test.
34 cal significance was tested with a one-sided paired t test.
35 nd 5D flow using a signed-rank or two-tailed paired t test.
36 lated and values were compared by means of a paired t test.
37 tested for statistical significance with the paired t test.
38 contrast-to-noise ratios (CNRs) by using the paired t test.
39 mparisons using Dunnett or Tukey methods and paired t test.
40 uble and single fields were compared using a paired t test.
41 ntion and non-intervention hospitals using a paired t test.
42 Signal intensity was evaluated by using a paired t test.
43 after sonication were compared by using the paired t test.
44 and the influence of BMI were evaluated via paired t test.
45 parisons within groups were performed with a paired t test.
46 cell viabilities were compared by using the paired t test.
47 NS were compared to prestimulus values using paired t test.
48 Comparisons were made by using a paired t test.
49 d with the DBM method and Student two-tailed paired t test.
50 tistical analysis was performed by using the paired t test.
51 .5 and 3.0 T were analyzed with a two-sample paired t test.
52 es multivariate analysis of variance and the paired t test.
53 e and lesions in patients were tested with a paired t test.
54 were evaluated and assessed by using Student paired t test.
55 ts were calculated and compared by using the paired t test.
56 tial function, and data were compared with a paired t test.
57 The PET uptake was compared using a paired t test.
58 Statistical comparisons were made using the paired t test.
59 d statistical significance was tested with a paired t test.
60 ing examinations were performed by using the paired t test.
61 dalities were determined with the two-tailed paired t test.
62 ty of statistical testing, especially of the paired t-test.
63 igned rank test, and the JSW was compared by paired t-test.
64 nd post-laser IOP values were compared using paired t-test.
65 e groups were compared with McNemar test and paired t-test.
66 Data were analyzed with paired t tests.
67 evaluated by using two-tailed nonpaired and paired t tests.
68 ast-to-noise differences were evaluated with paired t tests.
69 ere performed using analysis of variance and paired t tests.
70 was performed with Wilcoxon signed rank and paired t tests.
71 mean values in each phase were compared with paired t tests.
72 lustered on subjects was used, together with paired t tests.
73 d posttherapy studies were compared by using paired t tests.
74 Data were analyzed with multiple paired t tests.
75 re- and postdiet condition were tested using paired t tests.
76 and relative function were compared by using paired t tests.
77 stole) were quantified and compared by using paired t tests.
78 d-measures analysis of variance, followed by paired t tests.
79 on comparisons were made using McNemar's and paired t tests.
80 Statistical comparisons used paired t tests.
81 ifferences in tube voltage, were tested with paired t tests.
82 fter treatment suspension were assessed with paired t tests.
83 er 5 y in young adulthood through the use of paired t tests.
84 (VDV), were compared between visits by using paired t tests.
85 f-interest (ROI) size were compared by using paired t tests.
86 y repeated-measures analysis of variance and paired t tests.
87 values in the ICS treatment period by using paired t tests.
88 and health outcome measures evaluated using paired t tests.
89 mpared before and after the SEE program with paired t tests.
90 etween groups using analysis of variance and paired t-tests.
91 , with post hoc analysis employing ANOVA and paired t-tests.
92 nalysis of variance with post hoc two-tailed paired t-tests.
93 ect longitudinal changes were assessed using paired t-tests.
94 those after placebo administration by using paired t testing.
95 repeated-measures analysis of variance, and paired t testing.
96 was determined with the Student t test, the paired t test, a mixed random effects model, one-way ana
97 n with paired comparison procedures by using paired t tests across individual time points supplemente
102 Data were analyzed by using a combination of paired t tests, analysis of variance, contingency tables
103 S </= 3 + 4 and GS >/= 4 + 3 tumors by using paired t tests, analysis of variance, receiver operating
109 nostic confidence were compared by using the paired t test and Mann-Whitney U test, respectively.
111 d statistical analysis involving a voxelwise paired t test and one-way analysis of variance for metab
113 measures analysis of variance with post hoc paired t test and Skillings-Mack test with post hoc Wilc
115 atistical analysis was performed by 2-tailed paired t test and with nonparametric tests where appropr
117 n FBP and ADMIRE were compared by using both paired t tests and analysis of variance tests at the 95%
122 of variance with multiple comparisons and/or paired t tests and regression analysis were used for ana
123 of variance with multiple comparisons and/or paired t tests and regression analysis, as appropriate.
125 Variables were expressed as mean +/- SD; paired t-test and chi(2) test were used as appropriate.
127 ere compared with those of fellow eyes using paired t-tests and with those of control eyes using inde
128 r (11)C-tariquidar (+27% +/- 15%, P = 0.014, paired t test) and (11)C-elacridar (+21% +/- 15%, P = 0.
129 4 versus 8017 +/- 1103 micromol/d; P < 0.03, paired t test) and NO(2)/NO(3) (18.1 +/- 1.1 versus 22.9
130 creased orientation dispersion (P < 0.001 by paired t-test) and lower fractional anisotropy (P < 0.00
131 ' normal-appearing cortical grey matter T2* (paired t-test) and with mean cortical T2* in controls (l
132 with DXA, did not differ from DXA (P = .15, paired t test), and was able to identify osteoporosis (a
133 ysis was performed with the chi(2) test, the paired t test, and analysis of variance with repeated me
135 sis, repeated-measures analysis of variance, paired t test, and Bland-Altman analysis were used; for
138 distributed variables were compared by using paired t tests, and categorical data were compared by us
140 ponders and nonresponders were analyzed with paired t tests, and OS was calculated with the Kaplan-Me
141 tabolism between on and off conditions using paired t tests, and Pearson linear correlations were use
143 r-observer reproducibility, unpaired t-test, paired t-test, and Bland-Altman analyses to determine li
146 glucose transporter, and hexokinase assays (paired t test), as well as pharmacologic assays against
147 sis of variance and Bland-Altman analysis; a paired t test assessed change from baseline to after tre
149 ) significantly decreased by 3.5% (P = .012, paired t test) at 1 month and 4.2% (P = .007) at 3 month
151 ignificant difference tests, independent and paired t tests, Bland and Altman analyses, correlations,
156 ion effects of FA were evaluated by 2-tailed paired t test comparison of mean 5-minute preinjection a
162 anges during treatment were determined using paired t-tests corrected for multiple hypothesis testing
164 tireader multicase data and with the Student paired t test for analysis of observer-specific paired d
165 arison of CT fluoroscopy times, a two-tailed paired t test for comparison of age and tumor size, and
166 yses were performed by using a single-tailed paired t test for comparison of CT fluoroscopy times, a
167 -69 versus steady state (days 70-182) used a paired t test for continuous endpoints or Kappa statisti
168 (6-month) data were compared using Student's paired t test for parametric data and the Wilcoxon match
169 othelium, and the opposite pattern with VWF (paired t test for TM and EPCR, each P < .001; for VWF, P
170 tatistical significance was determined using paired t testing for longitudinal imaging and 2-way ANOV
173 fferences in mound volume were detected with paired t tests in 14 patients with early and late sonogr
174 n change of FA for regions that survived the paired t tests in patients treated with chemotherapy.
175 n detectability than 2D (P < 0.025, 2-tailed paired t test) in patients of normal size (body mass ind
177 ction and autorefraction were compared using paired t-tests, intraclass correlations, and Bland-Altma
181 tistical analysis was performed by using the paired t test, linear regression, and Bland-Altman analy
182 d with microsphere MBF measurements by using paired t tests, linear correlation, and Bland-Altman ana
183 intracellular volume fraction (P = 0.015 by paired t-test), lower myelin-sensitive contrast (P = 0.0
185 ally by means of descriptive statistics, non-paired t-test, Mann-Whitney rank sum test, Spearman rank
186 e analyzed using descriptive statistics, the paired t test, McNemar test, and a general linear model.
187 tatistical analysis was conducted by using a paired t test, multilevel analysis, and analysis of cova
189 ycan synthesis to 43% of controls (P < 0.02, paired t-test; n = 16) and produced a relative inhibitio
190 ially expressed genes, results from standard paired t-test of normalized data are compared with those
191 ant differences between both methods using a paired t-test of the results on a 95% confidence level.
192 ise on circulating miRNAs was assessed using paired t-tests of baseline and post-training expression
194 ve and operative groups were compared using: paired t test on a propensity score-matched subset and m
197 Within-group changes were analyzed with paired t tests or repeated measures analysis of variance
198 tion, the k1 and k2 significantly increased (paired t test P = 0.046 and P = 0.023, respectively).
200 NNA treatment (mean 42.9% [range 12.0-62.1]; paired t test p=0.0070), which was sustained for up to 2
202 TESv2 (mean change 0.97 +/- 1.77; two-tailed paired t-test P = 0.003) and the CMTESv2-R (mean change
203 year (mean change 2.24 +/- 3.09; two-tailed paired t-test P = 0.009) and over 2 years (mean change 4
204 Sv2-R (mean change 1.21 +/- 2.52; two-tailed paired t-test P = 0.009) increase significantly with res
205 years (mean change 4.00 +/- 3.79; two-tailed paired t-test P = 0.031) with respective standardized re
210 cts with SCH (19.5 +/- 5.3 vs. 23.7 +/- 4.1, paired t test, p < .0001); however, no correlations were
215 compared with matched normal breast tissues (paired t test, P < 0.0001) and a general inverse correla
219 ased and ALCS depth increased significantly (paired t-test, P < 0.01); no change in RNFL thickness wa
221 ples (mean yield = 7.6 micro g/two brushes) (paired t test: p < 0.001), while DNA yields from cheek a
225 ose of the phenotypically wild-type retinas (paired t-test; P < 0.01 and P < 0.01, respectively).
228 in patients with TLE than controls (p<0.05, paired t-test), particularly to neocortical regions incl
229 left carotid arteries were analyzed by using paired t tests; possible sex differences, by using unpai
236 acquired 120 min after injection (P < 0.001, paired t test; signal-to-noise ratio at 60 min after inj
238 , 0.82 +/- 0.11 and 0.84 +/- 0.10; Student's paired t-test, t = 2.79, P = 0.02; t = 2.80, P = 0.02; a
239 +/- 1.4 to 5.5 +/- 1.2 l min(-1) (P = 0.003, paired t test), tended to decrease stroke volume from 97
243 ges during the 12-month follow-up period and paired t tests to compare HSK-affected eyes with fellow
246 ogic test scores and whole-brain voxel-based paired t tests to study changes in WM fractional anisotr
248 sets for each group were then compared using paired t-tests to detect differences between the 2 popul
249 ally tested for intraindividual differences (paired t tests) to avoid effects resulting from variatio
257 was used to compare image rating scores, the paired t test was used to compare CRs, and kappa statist
263 sures general linear model and the Student's paired t test were used to analyze changes in laboratory
265 barriers that contribute to nonadherence and paired t tests were conducted for the preimplementation
274 naccuracies across sound-masking levels, and paired t tests were used to compare each sound-masking l
280 d using conditional logistic regression, and paired t tests were used to evaluate case-control differ
284 nt analyses, multiple linear regression, and paired t tests were used to select biomarkers of interes
289 Discriminant validity was described using paired t tests, whereas internal consistency was describ
290 27.2 +/- 13.1 mL/min per 1.73 m (P<0.001 on paired t test), which represents a 29.2% drop in the ser
291 ean difference 11.9 +/- 6.0 mum, P < 0.0001, paired t-test), while there was no significant differenc
292 ween cleaning methods were compared by using paired t tests with Bonferroni correction for 3 comparis
293 95% confidence interval, 0.21-0.05; post hoc paired t test) with reduced penetration-aspiration score
294 sample, we performed responsiveness testing (paired t tests) with 75 patients with HF receiving inter
295 +/- 15.2% (66.1 +/- 146 feet, p < 0.0001, by paired t test), with an intraclass correlation coefficie
297 McNemar test and procedural times by using a paired t test, with P < .05 indicating a significant dif
298 were compared in the two groups by means of paired t test, with subsequent histologic analysis to co
299 Statistical analysis was performed by using paired t tests, with P<.05 considered to indicate a sign