コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 , death) was compared between regimens using Poisson regression.
2 ors for ESBL-E acquisition in hospital using Poisson regression.
3 Subgroups were compared with Poisson regression.
4 os for women versus men were estimated using Poisson regression.
5 d non-Indigenous children by use of modified Poisson regression.
6 -15) using data from a systematic review and Poisson regression.
7 who remained to be treated using a modified Poisson regression.
8 as an absolute margin of 0.5% determined by Poisson regression.
9 the increase in 2017-2019 vs 2014-2016 using Poisson regression.
10 fferences by AIDS status and over time using Poisson regression.
11 s determined using multilevel, mixed-effects Poisson regression.
12 d factors associated with viral rebound with Poisson regression.
13 were also assessed in donors using modified Poisson regression.
14 using relative and absolute risk models via Poisson regression.
15 ed incidence rates of WL were analyzed using Poisson regression.
16 pre-vaccination (baseline) were evaluated by Poisson regression.
17 gnosed asthma were computed using a modified Poisson regression.
18 h experiencing a serious adverse event using Poisson regression.
19 1 or PM2.5 were evaluated with a time-series Poisson regression.
20 g Fisher's exact test and bivariate modified Poisson regression.
21 mple) by treatment arm were calculated using Poisson regression.
22 r age, sex, race/ethnicity, and season using Poisson regression.
23 oup, and relative rates were estimated using Poisson regression.
24 CLABSI incidence rates were compared using Poisson regression.
25 cidence rate ratios (IRRs) were estimated by Poisson regression.
26 d using generalized estimating equations for Poisson regression.
27 ence rate ratios (IRRs) were estimated using Poisson regression.
28 95% confidence intervals were calculated by Poisson regression.
29 x proportional hazards, competing risks, and Poisson regression.
30 trends were estimated by linear or piecewise Poisson regression.
31 who remained to be treated using a modified Poisson regression.
32 sis were respectively analysed using Cox and Poisson regression.
33 ons, and mortality between HEU and HUU using Poisson regression.
34 s and rate differences were determined using Poisson regression.
35 lence ratios with 95% CIs from multivariable Poisson regression.
36 ulated, and trend tests were conducted using Poisson regression.
37 infection in each period were assessed using Poisson regression.
38 ciated with MVPA were estimated using survey Poisson regressions.
39 yndrome and outcome using generalized linear Poisson regression adjusted for age, injury mechanism, I
42 dence rate ratio (IRRs) were estimated using Poisson regressions, adjusted for sociodemographics, com
43 atios were estimated following multivariable Poisson regression, adjusting for age, sex, ethnicity, s
44 ce rate ratios (aIRRs) were calculated using Poisson regression, adjusting for demographic and clinic
45 al and FVC of <80% predicted) using modified Poisson regression, adjusting for relevant confounders.
46 revalence ratios (PRs) and differences using Poisson regression, also examining sex-specific relation
51 ce ratios (SIRs) and, for SCC, multivariable Poisson regression analysis of SIR ratios, adjusting for
54 econd, based on results from the first step, Poisson regression analysis was used to derive the final
56 22 calendar years, 14 geographic areas, and Poisson regression analysis was used to quantify the eff
62 concurrent medications were estimated using Poisson regression and inverse probability of treatment
64 were compared between treatment groups with Poisson regression and one-inflated beta regression, res
68 sk ratios (RRs) were obtained using modified Poisson regression and weighted risk differences (RDs) u
69 nal hazards regression, logistic regression, Poisson regression, and generalized linear model with ga
73 asis' (RAMMIE) method and the improved quasi-Poisson regression-based method known as 'Farrington Fle
74 rming within each city were characterized as Poisson regression coefficients describing change in abu
75 Rs) and 95% confidence intervals (CIs) using Poisson regression, controlling for potential confoundin
82 nce rate ratios (IRRs) were calculated using Poisson regression for DLBCL risk in relation to HLA mis
85 tiation and continuation were assessed using Poisson regression in univariate and multivariate analys
87 ted PrEP uptake and continuation, and robust Poisson regression methods were used to identify correla
89 analyses evaluated day 0-69 findings using a Poisson regression model accounting for overdispersion.
91 ot in outbreak over the same period, using a Poisson regression model adjusting for correlation withi
93 phils >/=300 cells per muL), analysed with a Poisson regression model corrected for overdispersion wi
100 al logistic regression model and conditional Poisson regression model were used to estimate the risks
101 using negative binomial regression model and Poisson regression model with a robust variance estimato
102 blocker use and outcomes were analyzed using Poisson regression model with robust standard errors for
103 significant overdispersion (invalidating the Poisson regression model) and residual autocorrelation (
113 gistic regression for AF detection rate, and Poisson regression modelling for CHA2DS2-VASc scores.
119 cific associations were estimated with quasi-Poisson regression models and then pooled by random-effe
121 ppression CD4 count <200 and >=200 cells/uL, Poisson regression models estimated hospitalization inci
125 s of viral suppression were determined using Poisson regression models incorporating RDS-II weights.
126 P. vivax parasite prevalence, and multilevel Poisson regression models showed that such differences w
128 lyzed for incident asthma exacerbations with Poisson regression models that included clinical measure
133 a, and used generalized estimating equations Poisson regression models to estimate incidence rate rat
144 nt discharge data, multistate and log-linear Poisson regression models were used to calculate hospita
151 Coarsened exact matching techniques and Poisson regression models were used to estimate the risk
157 alent and incident DSPN were estimated using Poisson regression models with a robust error variance a
158 edding (VL > 40 copies/mL) were estimated by Poisson regression models with generalized estimating eq
164 ence after IRS were assessed by season using Poisson regression models with robust standard errors, c
167 fic mental disorder, we estimated MRRs using Poisson regression models, adjusting for sex, age, and c
192 tiveness was estimated by using multivariate Poisson regression models; effectiveness was allowed to
193 tiveness (VE), using unadjusted and adjusted Poisson regression of cytology (HSIL) and histopathology
195 risk factor associations were determined by Poisson regression (plaque presence), negative binominal
197 (CIMT) at baseline (2004) and used modified Poisson regression (robust error variance) to estimate p
198 tage renal disease (ESRD) were calculated by Poisson regression stratified by age and adjusted for et
200 n, region, and ethnicity were examined using Poisson regression, taking clustering within general pra
204 omist-drawn blood cultures was modeled using Poisson regression to compare the 12-month intervention
207 te of the first offered appointment; we used Poisson regression to compare the proportion of women wh
208 y state and age group, we used mixed-effects Poisson regression to determine individual-level and dis
210 d by trajectory group and performed adjusted Poisson regression to estimate adjusted incidence rate r
213 or decompensations, excluding HCC) and used Poisson regression to estimate incidence rate ratios.
215 infection with the general population, used Poisson regression to evaluate anal cancer incidence amo
217 verse probability of treatment weighting and Poisson regression to evaluate RVE in preventing influen
218 families, we used Mantel-Haenszel tests and Poisson regressions to estimate incidence rate ratios fo
220 ge involved a county-level time series quasi-Poisson regression, using a distributed lag nonlinear mo
226 eometric mean reproductive hormones, whereas Poisson regression was used to assess risk of sporadic a
233 accounting for the competing risk of death; Poisson regression was used to compare rates of NCD occu
262 Incidence rate ratios were calculated using Poisson regressions while adjusting for sociodemographic
270 and were related to SGA risk with the use of Poisson regression with confounder adjustment; linear sp
271 bic-restricted splines and multivariable log-Poisson regression with empirical standard errors were u
274 HIV incidence estimated using multivariable Poisson regression with generalized estimating equations
275 nce intervals were estimated from log-linked Poisson regression with generalized estimating equations
277 quipment use was examined using multivariate Poisson regression with generalized estimating equations
279 months after each of these were analysed by Poisson regression with invasive interval cancer screen
280 Survey of Family Growth using multivariable Poisson regression with multiple covariates and adjustme
282 -adjusted DDLT rates using nested multilevel Poisson regression with random intercepts for DSA and tr
283 s of no return to baseline were estimated by Poisson regression with robust error variance and adjust
287 s, were calculated in STATA using a modified Poisson regression with robust error variances to obtain
290 owth and obesity were assessed by linear and Poisson regression with robust standard errors, adjustin
292 012 and 2015 for several risk factors, using Poisson regression with robust variance and a bootstrap-
297 avior, and clinical characteristics, we used Poisson regression with robust variance to estimate prev
298 d incidence rate ratios were estimated using Poisson regression with robust variance while accounting
299 ios (IRRs) associated with abortion, we used Poisson regression with the logarithm of woman-years at