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 oss all age and EF groups had markedly lower median survival.
2 was associated with worsening FEV1 and lower median survival.
3 hibition of tumor growth and prolonged mouse median survival.
4 with rapid onset of tetraparesis and shorter median survival.
5 ete tumour remission or an increase in their median survival.
6 n adult primary brain tumor and has a dismal median survival.
8 least one intensive procedure) had a shorter median survival (0.7 versus 2.1 years; P<0.001), spent a
10 e with wild-type tumors, CRT did not prolong median survival (1.3 v 1.8 years; HR, 1.14; 95% CI, 0.63
11 survival, 14.2 (13.1-15.4) years; and HLA-no median survival, 12.1 (10.9-13.3 years) years; P<0.01, l
12 s (median survival=40days), cisplatin alone (median survival=12days) or saline-treated controls (medi
13 ypermetabolism was associated with a reduced median survival [14.6 compared with 21.4 mo, respectivel
14 nfidence interval, 14.0-20.2) years; HLA-low median survival, 14.2 (13.1-15.4) years; and HLA-no medi
15 70%, P<0.01), and a trend for longer overall median survival (15.4 versus 9.3 months, P=0.72) yet not
16 265 days), compared with unvaccinated mice (median survival, 150 days; P = .002), mice given only LM
17 50 days; P = .002), mice given only LM-Kras (median survival, 150 days; P = .050), and unvaccinated m
18 tated and worst in triple-negative patients: median survival, 16 vs 2.3 years (HR, 5.1; 95% CI, 3.2-8
19 ee of HLA donor-recipient matching: HLA-high median survival, 17.1 (95% confidence interval, 14.0-20.
21 roup than in the total pancreatectomy group (median survival 19 months vs 4 months, respectively).
22 MM patients without prior knowledge of MGUS (median survival, 2.1 years), although MM patients with (
23 0.77-0.96; P < .01) better overall survival (median survival, 2.8 years) than MM patients without pri
25 HER2-positive subtype displayed the longest median survival (21.0 months); patients with triple-nega
26 urvival was recorded between the two groups (median survival 23.4 months [95% CI 20.9-24.8] with doce
27 ted with improved survival compared with UR (median survival, 26 months v 21 months, respectively; st
28 nged survival and reduced PanIN progression (median survival, 265 days), compared with unvaccinated m
30 patients with EGFR mutations had the longest median survival (3.51 years; 95% CI, 2.89 to 5.5 years),
31 port cells succumbed to bone marrow failure (median survival, 328 days) characteristic of myelodyspla
33 atin in conventional un-PEGylated particles (median survival=40days), cisplatin alone (median surviva
34 d rate in Bap1(+/-) mice than in WT animals (median survival, 43 weeks vs. 55 weeks after initial exp
35 cohort of 590 patients with advanced cancer (median survival, 5.4 months), 71% wanted to be told thei
38 ached </= 0.2 ng/mL compared with > 4 ng/mL (median survival, 60.4 v 22.2 months, respectively; P < .
39 raft survival in patients with IPF (adjusted median survival, 65.2 months [interquartile range {IQR},
41 001) but not in patients with COPD (adjusted median survival, 67.7 months [IQR, 25.2-89.6 months] vs
43 io was 0.98 (95% CI, 0.80 to 1.20; P = .847; median survival, 70 months) for SOC + Cel and 0.86 (95%
45 is than those without severe disease (n=113; median survival 8.0 years, 95% CI 6.5-9.5 vs 10.3 years,
49 pitalization; 8.8% survived the efforts, and median survival after leaving the hospital was 10.5 mont
54 as been demonstrated to significantly extend median survival and achieve a high rate of complete tumo
56 ear relationship identified between expected median survival and EOR argues against a surgical manage
59 homa in mice at seemingly similar paces with median survival around 10 and 11 weeks, respectively, co
61 nt to normal level, and significantly longer median survival as compared to free drugs or untargeted
62 rosis (IPF) is a devastating disease, with a median survival as short as 3 years from the time of dia
63 g patients with decompensated cirrhosis, the median survival benefit was 31 days, and it was not cost
65 codeleted tumors, there was no difference in median survival by treatment arm (2.6 v 2.7 years; HR =
66 re typically have more indolent disease with median survivals close to 25 years, and Ig-mutated CLL,
70 lidomide-based therapy results in subsequent median survival exceeding 5 years; for these patients, F
73 -) and Cd74(-/-) mice demonstrated decreased median survival following hyperoxia compared to WT mice.
82 nally related to the underlying CLL, and the median survival for these patients is approximately 1 ye
84 the GI tract to treat, associated with poor median survivals for metastatic disease and significant,
85 the age- and sex-matched control population; median survivals for patients younger than 60 years are
86 ficantly impaired tumor growth and prolonged median survival from 13 d (phosphate-buffered saline) to
87 these mice was associated with an increased median survival from approximately 5.5 to 7.5 mo and inc
88 o percent of patients required dialysis, and median survival from commencement of dialysis was 5.2 ye
91 om onset was 9.8 years (95% CI 8.8-10.7) and median survival from enrolment was 1.8 years (0.9-2.7).
96 There was a significant increase in overall median survival from the 1970s to 2000s (2 vs. 8 months;
101 ups treated with 3.7 and 7.4 MBq exhibited a median survival greater than 300 and 227 d, respectively
103 centration AgNP has no negative influence on median survival; however, these flies appeared uniformly
111 ive-intent surgical resections, resulting in median survival in this subgroup that exceed 5 years.
112 method, which shows significant extension of median survival in two patient-derived BTIC xenograft mo
115 ents, further treatment options are limited, median survival is <6 months, and consideration should b
116 ression and hinders effective treatment; the median survival is 16 mo despite standard-of-care therap
120 omatic, and this, in combination with a long median survival, led to the initial studies of observing
121 is highly invasive and uniformly fatal, with median survival<20months after diagnosis even with the m
123 Because of their relatively long overall median survival, more aggressive treatments are typicall
124 elivered in brain penetrating nanoparticles (median survival not reached; 80% long-term survivors) co
126 advanced cancer diagnosis for patients with median survival of 1 year or less, and progressive disea
128 rtality of 44.4/100 person-years (PYs) and a median survival of 13.5 months after the diagnosis of CM
129 adiation and chemotherapy, only results in a median survival of 14 months, underscoring the importanc
130 chemotherapy, the prognosis is poor, with a median survival of 16 to 19 months and poor quality of l
134 e severely impaired cardiac function, with a median survival of 22 wk, despite otherwise unaltered sy
135 for 23% of all cases, was associated with a median survival of 23 months and a platinum resistance r
136 A total of 151 had NAFLD and 94 AFLD with median survival of 24 years and 20 years, respectively (
137 of 2.7/100 PYs (P < 0.001) and an estimated median survival of 27.0 years after the diagnosis of CMV
138 ts receiving surgical therapy (n = 25) had a median survival of 27.8 months, significantly superior t
139 poorer survival than the rest of the cohort (median survival of 28 vs 163 months, log-rank test P<0.0
140 and these tumors proliferate rapidly with a median survival of 28-days accompanied with histological
142 ts experience frequent relapses resulting in median survival of 3 to 5 years, requiring more efficien
144 s who received a DT of more than 55 Gy had a median survival of 32.8 mo, compared with 7.2 mo in pati
146 a platinum resistance rate of 63%, versus a median survival of 46 months and platinum resistance rat
147 6 patients developed progressive CLL, with a median survival of 51 months after disease progression.
148 associated with the highest survival with a median survival of 53.0% (range, 26.0-72.0), whereas def
149 adliest cancers in western countries, with a median survival of 6 months and an extremely low percent
150 has resulted in marrow CR rates of 55% and a median survival of 6 to 7 months when given to patients
151 n overall response rates of 40% to 50% and a median survival of 6.5 months in a similar refractory-re
152 studied for the creation of the DS-GPA had a median survival of 7 months from the time of initial tre
153 atients (<10 points) demonstrating excellent median survival of 70.6 months, significantly superior t
156 those who preferred inotropes over LVAD had median survival of 9.0 months (interquartile range, 3.1-
157 and increased risk of death due to lymphoma (median survival of 9.5 years with BCL2 mutations vs 20.4
161 rity of SMZLs show an indolent course with a median survival of approximately 10 years, nearly 30% of
163 espite intensive therapeutic strategies, the median survival of GBM patients has remained dismal over
167 studies, (211)At-B10-30F11 RIT improved the median survival of leukemic mice in a dose-dependent fas
171 with BA and ibrutinib markedly improved the median survival of mice engrafted with the MCL cells.
172 esveratrol treatment significantly increased median survival of mice with HF, lessened cardiac fibros
173 ression in the prostate tumors (n=8); with a median survival of more than 60 days compared to 12 days
182 potent therapeutic effect and prolonged the median survival of TET1-high AML mice over three fold.
186 40, 95% CI, 0.27 to 0.60, P < .001), and the median survival of those with codeleted tumors treated w
188 ies also defines better outcome groups, with median survivals of 15.9 versus 9.2 months (P = 0.029) a
189 o characterize the incidence proportions and median survivals of patients with breast cancer and brai
190 MD treatment was further shown to extend the median survival period from less than 20days in the cont
197 (+) T-cell tumor infiltration, and increased median survival, relative to control mice immunized with
199 ons: both groups had a significantly shorter median survival than patients with a margin of greater t
200 R1 had higher rates of relapse and a shorter median survival than patients with ovarian cancers that
201 ntinued metformin had a significantly longer median survival than those who discontinued metformin (1
202 rs incidentally diagnosed demonstrate longer median survival than tumors discovered only when the pat
203 iously reported IDEC-131-treated allografts, median survival time (35 +/- 31 days) was significantly
204 cal follow-up showed a significantly shorter median survival time (4.1 y, age-adjusted hazard ratios
205 tment with MPA-loaded nanogels increased the median survival time (MST) of lupus-prone NZB/W F1 mice
206 nvasion and worse disease-specific survival (median survival time 20.3 versus 43.9 months, log-rank P
208 in patients diagnosed in more recent years (median survival time 3.3 years [95% CI 3.0-3.8] in 2001
209 was 65% overall, 48% in the BDex+AA cohort (median survival time 821 days), and 76% in patients who
211 ediction was assessed by using difference in median survival time and area under the curve with time-
212 r differentiation according to difference in median survival time between high- and low-risk groups (
215 progressing neurodegenerative disease with a median survival time from diagnosis of 1.5-3 years.
217 amelteon or melatonin significantly improved median survival time in rats (sepsis/melatonin [0.1 mg/k
222 hose with an SUVr of at least 2.5, who had a median survival time of 10.1 (95% CI: 2.4, 15.9; P = .00
223 deaths from lung cancer were documented with median survival time of 10.3 months (interquartile range
225 nths), 71.6% of patients were deceased, with median survival time of 11 months for those who died.
226 tients with SUVr of less than 1.7, who had a median survival time of 23.1 months (95% confidence inte
233 prevalence of idiopathic pulmonary fibrosis, median survival time of patients, and potential risk fac
235 and breast cancer xenografts and doubled the median survival time of TCL1-Tg:p53(-/-) mice, which dev
237 classical predisposing host factors, and the median survival time was <4 months after diagnosis.
238 low-up of 28.5 months (for living patients), median survival time was 11.8 months (95% CI, 7.4 to 19.
242 after a diagnosis of esophageal cancer, the median survival time was 14.9 months (IQR, 7.1-52.3 mo)
246 years [SD 7.2], 54% female, 91% white), the median survival time was 3.8 years (95% CI 3.5-3.8).
250 estimated the time ratio (relative change in median survival time) per 100 working level months (rado
255 ast 8.2% of the subjects in this cohort, and median survival times among men with LOY were 5.5 years
256 h R0, R1 (<1 mm), and R1 (direct) status the median survival times and 5-year survival rates were 41.
259 with those without diabetes (P < .001), with median survival times of 3 months for long-term diabetic
260 with those without diabetes (P = .02), with median survival times of 9 months for long-term diabetic
261 ligand mismatch significantly prolonged the median survival to 163 d compared with vehicle controls
265 0.63 (95% CI 0.50-0.79; one-sided p<0.0001); median survival was 10.6 months (95% CI 9.1-12.1) for re
276 n follow-up of 40 months (7-109 months), the median survival was 40 months versus 53 months in the AF
278 was 20 months (95% CI, 16 to 26 months), and median survival was 49 months (95% CI, 40 months to not
286 l subtype who underwent trimodality therapy, median survival was extended from 14.5 months to 23.4 mo
291 3 [44%] of 1315 in other African countries), median survival was shorter in the other African countri
296 After PSM, the 3-year survival rates and median survival were 44.9% and 27.2 (95% confidence inte
297 of Mayo patients were followed until death; median survivals were 19.8 years in ET (n = 292), 13.5 P
298 mutant zebrafish have significantly reduced median survival with death occurring 5 days post-fertili
300 prostate DKO) exhibited a markedly increased median survival with reduced tumor size and proliferatio
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。