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1 en than in women (P<0.0001, Cox proportional hazards model).
2 er (using the multivariable Cox proportional hazards model).
3 for a previously published Cox proportional hazards model.
4 imated with a multivariable Cox proportional hazards model.
5 splant-free survival with a Cox proportional hazards model.
6 l were examined using the Cox's proportional hazards model.
7 we further adjusted using a Cox proportional hazards model.
8 were estimated by using the Cox proportional hazards model.
9 s were investigated using a Cox proportional hazards model.
10 m standard analyses using a Cox proportional hazards model.
11 ly relevant covariates in a Cox proportional hazards model.
12 Rs) were estimated with the Cox proportional hazards model.
13 separately, using adjusted Cox proportional hazards models.
14 n-Meier curves and adjusted Cox proportional hazards models.
15 of a KT were examined using Cox proportional hazards models.
16 th mortality using adjusted Cox proportional hazards models.
17 ere defined in time-updated Cox proportional hazards models.
18 sing multivariable-adjusted Cox proportional hazards models.
19 a sequence of multivariable Cox proportional hazards models.
20 tervals were obtained using Cox proportional hazards models.
21 ociations were tested using Cox proportional hazards models.
22 xamined with time-dependent Cox proportional hazards models.
23 rtality were assessed using Cox proportional hazards models.
24 cases) were estimated using Cox proportional hazards models.
25 survival was performed with Cox proportional hazards models.
26 val (OS) were analyzed with Cox proportional hazards models.
27 ultivariate regression with Cox proportional hazards models.
28 valuated using log-rank and Cox proportional hazards models.
29 and linear regression, and Cox proportional hazards models.
30 onal multivariable-adjusted Cox proportional hazards models.
31 s estimated with the use of Cox proportional hazards models.
32 pilepsy were assessed using Cox proportional hazards models.
33 me to binary outcomes using Cox proportional hazards models.
34 mortality using univariate Cox proportional hazards models.
35 time-dependent covariate in Cox proportional hazards models.
36 k of MCI was investigated using proportional hazards models.
37 ons with death and MI using Cox proportional hazards models.
38 ion based on residuals from Cox proportional hazards models.
39 andom and fixed effects and Cox proportional hazards models.
40 vival analysis and adjusted Cox proportional hazards models.
41 ea-based deprivation) using Cox proportional hazards models.
42 eloping breast cancer using Cox proportional hazards models.
43 (CIs) were estimated using Cox proportional hazards models.
44 timated using multivariable Cox proportional hazards models.
45 ife tables and time-varying Cox proportional hazards models.
46 l after ALS diagnosis using Cox proportional hazards models.
47 nivariate and multivariable Cox proportional hazards models.
48 sed using Andersen-Gill and Cox proportional hazards models.
49 ident all-cause mortality using proportional hazards models.
50 using survival analyses and Cox proportional hazards models.
51 te Inpatient Database using Cox proportional hazards models.
52 lative hazards with conditional proportional hazards models.
53 n or KT were examined using Cox proportional hazards models.
54 -Meier survival curves, and Cox proportional-hazards models.
55 ction among vaccinees using Cox proportional hazards models.
56 nt AF was examined by using Cox proportional hazards models.
57 curves were measured using Cox-proportional hazards models.
58 lity was investigated using Cox proportional hazards models.
59 sing multivariable-adjusted Cox proportional hazards models.
60 d untreated groups by using Cox proportional hazards models.
61 alyses were performed using Cox-proportional hazards models.
62 e rates (IRs) and developed Cox proportional hazards models.
63 the Kaplan-Meier method and Cox proportional hazards modeling.
64 using step-up and step-down Cox proportional hazards modeling.
65 n-Meyer curves and adjusted Cox proportional hazards modeling.
66 factors were identified by Cox proportional hazards modeling.
67 rate curves and univariate Cox proportional hazards modeling.
68 ing Kaplan-Meier method and Cox proportional hazards modeling.
69 lan-Meier survival analysis and proportional hazards modeling.
70 ivariable and multivariable Cox proportional hazards modeling.
71 ariables as predictors with Cox proportional hazards modelling.
75 mortality was assessed with Cox proportional hazards models adjusted for age, sex, AMD severity, VA,
78 ith SAR were analyzed using Cox proportional hazards models adjusted for clinicopathologic features a
79 e to death was studied with Cox proportional hazards models adjusted for demographic and clinical var
80 CRC-related survival using Cox proportional hazards models adjusted for demographic, tumor, and trea
84 otype and OS is assessed by Cox proportional hazards model adjusting for age, sex, International stag
85 admission, we constructed a Cox proportional hazards model adjusting for age, sex, race, and comorbid
86 idence intervals (CIs) from Cox proportional hazards models adjusting for baseline prognostic factors
87 nd multiple sclerosis using Cox proportional hazards models, adjusting for individual and contextual
89 rvival was assessed using a Cox proportional hazards model after adjusting for the propensity score f
91 d to receive an OLT using a Cox proportional hazards model and a generalized additive model with a lo
93 al (DSS) were assessed with Cox proportional hazards modeling and a competing risk analysis, respecti
99 derived using multivariate Cox proportional hazards models and standard clinical prediction rules.
100 ncy was assessed by using a Cox proportional hazards model, and a multiple variable model was examine
101 eier method, log-rank test, Cox proportional hazards models, and propensity score-matched analyses.
102 Kaplan-Meier analysis, and Cox proportional hazards models, as well, were developed to search for ri
107 fied multivariable-adjusted Cox proportional hazards models, black women and men were more likely to
108 ting for 34 covariates in a Cox proportional hazards model, borderline PH was associated with increas
109 e new Bayesian hierarchical Cox proportional hazards models, called the spike-and-slab lasso Cox, for
111 Using competing risk and Cox proportional hazards models, clinical factors at baseline and after t
112 cancer were estimated using Cox proportional hazards models, considering exposure as a time-varying v
119 n rehospitalization using a Cox proportional hazards model, following sequential adjustment for covar
120 ach outcome, we first ran a Cox proportional hazards model for each city, adjusting for prior cardiop
121 he hazard ratio, based on a Cox proportional hazards model for lisdexamfetamine vs placebo, was 0.09
126 ional Study, we constructed Cox proportional hazards models for CHD including age, pregnancy status,
128 r probability estimates and Cox proportional hazards models for post-HCT outcomes based on recipient
130 he primary analysis using a Cox proportional hazards model gave a mortality reduction over years 0-14
131 d all-cause mortality using Cox proportional hazards models; hazard ratios with 95% confidence interv
134 constructed a multivariate Cox proportional hazards model in which the impact of each covariate was
135 ng an age- and sex-adjusted Cox proportional-hazards model, in all participants and also after restri
136 or covariates, results from Cox proportional hazards models, including SBP and DBP, jointly suggested
137 In multivariable-adjusted Cox proportional hazards models, increasing years of baseline rotating ni
143 re enables analyses under a Cox proportional hazards model or Weibull regression model, and can accou
147 lyzed using a multivariable Cox proportional hazards model, providing hazard ratios (HRs) with 95% co
151 0.10-mg/m3 exposure level, Cox proportional hazards models showed significantly increased risk of mo
157 ozone using a two-pollutant Cox proportional-hazards model that controlled for demographic characteri
158 disability worsening by use of proportional hazards models that included OCT metrics and age, diseas
159 were tested with the use of Cox proportional hazards models that were adjusted for age, sex, body mas
164 actorial analysis using the Cox proportional hazards model to identify factors affecting survival (as
167 l adult population and used Cox proportional hazards modeling to estimate determinants of death.
173 rst developed multivariable Cox proportional hazards models to determine predictors of developing dep
175 panic-CRIC Studies, we used Cox proportional hazards models to determine the association between race
182 vascular Health Study using Cox proportional hazards models to examine the association between FGF23
186 ier survival and univariate Cox proportional hazards models to examine the effect of LSF on survival
187 for bankruptcy, we then fit Cox proportional hazards models to examine the relationship between bankr
192 dividual patient level with Cox proportional hazards models to quantify associations of creatinine-ba
196 ix exposure metrics and fit Cox proportional hazards models to the simulated data using the six metri
198 a propensity score-weighted Cox proportional hazards model using data from the British Association of
201 or disengagement based on a Cox proportional hazards model, using multiple imputation for missing dat
202 with multivariable adjusted Cox proportional hazards models, using the 120-129 mm Hg systolic blood p
215 treatment failure rates and Cox proportional hazards modeling was used to identify risk factors.
216 l variables and a penalised Cox proportional-hazards model, was used to compare method performance.
219 Using covariate-adjustment Cox proportional hazards models, we estimated associations of mean annual
223 and death calculated by the Cox proportional hazards model were compared with those of age-matched co
226 Kaplan-Meier estimation and Cox proportional hazards models were conducted to identify risk factors f
231 Unadjusted and adjusted Cox proportional hazards models were performed to compare outcomes by pat
234 ed at 130 SELECT sites, and Cox proportional hazards models were used in a modified intent-to-treat a
237 204 serum metabolites, and Cox proportional hazards models were used to analyze the longitudinal ass
266 B, hazard ratios (HRs) from Cox proportional hazards models were used to estimate incident exfoliatio
274 s used to estimate DSS, and Cox proportional hazards models were used to evaluate the association bet
275 ses and marginal structural Cox proportional hazards models were used to evaluate the relationship be
280 ial logistic regression and Cox proportional hazards models were used to model progression, CKD remis
285 ersen-Gill extension to the Cox proportional hazards model while accounting for the competing risk of
286 eled using a multivariable subdistributional hazards model while treating any other cause of death as
287 s were determined using the Cox proportional hazards model with a significance level set at P <0.05.
290 = .0075, respectively) and in a proportional hazards model with time-dependent covariates (adjusted h
291 and then performed a piece-wise proportional hazards modeling with 2 time periods: discharge to 90 da
293 tality was determined using Cox proportional hazards models with backward stepwise selection and incl
294 Multivariable-adjusted Cox proportional hazards models with cumulative updating of exposures wer
297 hierarchical multivariable Cox proportional hazards models with occurrence of depression as a time-v
299 fied multivariable-adjusted Cox proportional hazards modeling, with adjustment for time-updated covar
300 os (HRs) for death by using Cox proportional hazards models, with adjustment for age, sex, race/ethni
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