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1 corneal thickness (CCT), and graft survival (Kaplan-Meier analysis).
2 dure or drug dose adjustment, evaluated in a Kaplan-Meier analysis).
3 y end point was to compare overall survival (Kaplan-Meier analysis).
4 he recurrence-free curve was estimated using Kaplan-Meier analysis.
5 d overall recurrence were evaluated by using Kaplan-Meier analysis.
6 d probability of rebound and resistance with Kaplan-Meier analysis.
7 splantation graft survival was assessed with Kaplan-Meier analysis.
8 oth univariate and multivariate analysis and Kaplan-Meier analysis.
9 A, NRP-1, FOXO 3a and MelCAM were studied by Kaplan-Meier analysis.
10 Device longevity was estimated using Kaplan-Meier analysis.
11 The patency was evaluated by Kaplan-Meier analysis.
12 th graft survival was also explored by using Kaplan-Meier analysis.
13 Survival was analyzed by Kaplan-Meier analysis.
14 al of bladder cancer patients as revealed by Kaplan-Meier analysis.
15 ation of reduced recurrence-free survival by Kaplan-Meier analysis.
16 999 copies/mL) for 6, 9, or 12 months, using Kaplan-Meier analysis.
17 tive risk (lambda) and cumulative risk using Kaplan-Meier analysis.
18 number of photographs taken was evaluated by Kaplan-Meier analysis.
19 om from revascularization was estimated with Kaplan-Meier analysis.
20 stable microsatellites P = .0415), based on Kaplan-Meier analysis.
21 rates divided by incidence, as estimated by Kaplan-Meier analysis.
22 tional hazards regression model analysis and Kaplan-Meier analysis.
23 rvival (PFS) and overall survival (OS) using Kaplan-Meier analysis.
24 ion-free survival and overall survival using Kaplan-Meier analysis.
25 Survival was assessed using Kaplan-Meier analysis.
26 ar cumulative percentage of MAE was 12.5% by Kaplan-Meier analysis.
27 cause-specific survival (CSS), P = 0.012] by Kaplan-Meier analysis.
28 al hazards modeling and were evaluated using Kaplan-Meier analysis.
29 tuarial overall survival was calculated with Kaplan-Meier analysis.
30 and bone metastasis statuses was compared by Kaplan-Meier analysis.
31 Long-term survival was evaluated by Kaplan-Meier analysis.
32 ree survival (LPFS) were calculated by using Kaplan-Meier analysis.
33 m the first TACE session was calculated with Kaplan-Meier analysis.
34 cumulative incidence of PD was calculated by Kaplan-Meier analysis.
35 tients was assessed using Cox regression and Kaplan-Meier analysis.
36 iagnoses were obtained and used to perform a Kaplan-Meier analysis.
37 dney transplants at the same center by using Kaplan-Meier analysis.
38 the synthetic lethal gene is evaluated using Kaplan-Meier analysis.
39 recurrence free survival were explored using Kaplan-Meier analysis.
40 dementia and parkinsonism was estimated with Kaplan-Meier analysis.
41 Fisher exact test, analysis of variance, and Kaplan-Meier analysis.
42 and bone metastasis statuses was compared by Kaplan-Meier analysis.
43 n rank-sum tests, the Fisher exact test, and Kaplan-Meier analysis.
44 us immunosuppressant use was estimated using Kaplan-Meier analysis.
45 which was significant in both chi-square and Kaplan-Meier analysis.
46 ative risk of treatment failure by day 28 by Kaplan-Meier analysis.
47 associated genetic variants were assessed by Kaplan-Meier analysis.
49 e who did not have angiography, according to Kaplan-Meier analysis (281/3085 [12.8%] vs 480/4158 [16.
52 median follow-up of 5.2 (3.6, 6.9) years on Kaplan-Meier analysis, a significant nonlinear associati
56 overall survival discrimination, with use of Kaplan Meier analysis and a univariate Cox proportional
57 nt recipients 61 years of age or older using Kaplan- Meier analysis and Cox proportional hazard model
58 ters and survival time was assessed by using Kaplan-Meier analysis and a Cox proportional hazards mod
60 se Neuroimaging Initiative were evaluated by Kaplan-Meier analysis and analyses of variance and covar
61 sed mortality within 90 days of operation by Kaplan-Meier analysis and assessed the role of patient a
63 (2009-2019), comparing survival outcomes by Kaplan-Meier analysis and comparing other measures of ou
64 ated the probability of recanalisation using Kaplan-Meier analysis and conducted multivariate analysi
66 s and survival outcomes were investigated by Kaplan-Meier analysis and Cox proportional hazard models
67 tality were analyzed by NYHA IV status using Kaplan-Meier analysis and Cox proportional hazard models
69 Recurrence and survival were analyzed using Kaplan-Meier analysis and Cox proportional hazards model
75 idence of clinical outcome was determined by Kaplan-Meier analysis and Cox regression was used to eva
81 ere complete success rates at 24 months with Kaplan-Meier analysis and incidence of adverse events.
89 t macular atrophy after nAMD was examined by Kaplan-Meier analysis and proportional hazards regressio
93 Bi- and multivariable logistic regression, Kaplan-Meier analysis, and Cox proportional hazards mode
94 e evaluated with competing risks regression, Kaplan-Meier analysis, and Cox proportional hazards regr
96 Survival of the fellow eye was estimated by Kaplan-Meier analysis, and log-rank test was used to com
97 t and cumulative incidence were evaluated by Kaplan-Meier analysis, and relative risks were estimated
100 success of second glaucoma drainage devices (Kaplan-Meier analysis) at 1 year, 2 years, and 3 years w
102 esion revascularization (TLR) estimated with Kaplan-Meier analysis, clinical and hemodynamic improvem
105 respect to HNSCC staging were compared using Kaplan-Meier analysis, Cox proportional hazards regressi
106 and stage-based survival were compared using Kaplan-Meier analysis, Cox proportional-hazards regressi
125 points included 1-year survival, survival by Kaplan-Meier analysis, duration of ventilation, intensiv
134 =0.0050) and lower likelihood of survival on Kaplan-Meier analysis (hazard ratio 5.9, 95% CI 1.9-18.4
136 Successful trabeculectomies, determined by Kaplan-Meier analysis, in which patients have intraocula
146 gher colorectal cancer-specific mortality in Kaplan-Meier analysis (log-rank test, P < 0.0001), univa
147 iac risk factors and CMR were significant in Kaplan-Meier analysis (log-rank test, p = 0.0006 and p <
148 icantly with poor survival prognosis using a Kaplan-Meier analysis (log-rank test, P=5 x 10(-4)), sug
149 lant-free survival was investigated by using Kaplan-Meier analysis, log-rank tests, and Cox regressio
153 ariate adjusted outcomes were assessed using Kaplan-Meier analysis, multivariate cox regression, mult
160 ere randomized into eight treatment arms for Kaplan-Meier analysis of defined survival end-point (3.0
175 up vs 43.3% (565/1304) in the placebo group, Kaplan-Meier analysis of time to death by 1 year, P = .7
180 ssociated with survival from presentation in Kaplan-Meier analysis (p < 0.01), and loss of 1p36 and 1
183 antly lower overall mortality, determined by Kaplan-Meier analysis (P=.0047), univariate Cox regressi
201 nipulation and no AI at the time of implant, Kaplan-Meier analysis revealed that freedom from greater
240 Using unadjusted and adjusted Cox models and Kaplan-Meier analysis, there was no significant differen
243 learance kinetics, measured every 6 h, and a Kaplan-Meier analysis to compare parasite clearance kine
244 those with missing CSRS predictors, we used Kaplan-Meier analysis to describe the time to serious ar
245 Inverse probability weighting was used with Kaplan-Meier analysis to determine amputation-free survi
249 The associations were further delineated by Kaplan-Meier analysis using publicly available mRNA expr
253 Median renal survival from diagnosis by Kaplan-Meier analysis was 5.4 years, and median estimate
269 tory abilities of inflammation-based scores; Kaplan-Meier analysis was performed to plot the survival
273 as in patients with limited life expectancy, Kaplan-Meier analysis was repeated including only patien
276 mplications and of need for reoperation, and Kaplan-Meier analysis was used to assess graft survival
287 At 1 year, the rate of death from any cause (Kaplan-Meier analysis) was 30.7% with TAVI, as compared
288 l success at the last follow-up according to Kaplan-Meier analysis were 100% and 94.4% in bevacizumab
291 [CI], 0.71 to 1.15; P=0.41) and at 2 years (Kaplan-Meier analysis) were 33.9% in the TAVR group and
292 he 1-, 12-, and 24-month mortality rates (by Kaplan-Meier analysis) were 4.5%, 15.8%, and 15.8%, resp
293 CD20+ cells/hpf had worse graft survival in Kaplan-Meier analysis with a hazard ratio 4.56 (CI 1.07-
295 Overall survival (OS) was compared using Kaplan-Meier analysis with log-rank tests and multivaria
299 ropensity-matched cohorts and illustrated by Kaplan-Meier analysis with subgroup analysis for intermi