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1 h was 10 hours (interquartile range, 3.36-66 hours).
2 8 hours (95% confidence interval [CI]: 50-65 hours).
3 symptom onset to endovascular therapy = 5.2 hours).
4 t antenna, AuNPs reached the brain within an hour.
5 parin tubes and stored at 4 degrees C for 24 hours.
6 .01) compared with CAG performed at 12 to 24 hours.
7 eatment, and these increases persisted for 3 hours.
8 horacic echocardiography performed within 48 hours.
9 n of pacing therapy ranged from 19.7 to 35.7 hours.
10 s, but results returned to baseline after 48 hours.
11 as antibiotic administration in the first 24 hours.
12 1-2 hours), with a half-life of 5.2 to 10.9 hours.
13 significantly lower at 2 hours, but not at 4 hours.
14 revascularization, or stent thrombosis at 48 hours.
15 wild-type mice despite being higher after 24 hours.
16 they received combination therapy for >/=48 hours.
17 mg spironolactone (usual care) daily for 96 hours.
18 complete hundreds of samples in a matter of hours.
19 bbons via the cell's cytoplasm takes several hours.
20 pplementation at 6, 12, and 24 postoperative hours.
21 bside flight which are stronger in afternoon hours.
22 rocess could be quickly completed within two hours.
23 f patients with resolution of symptoms at 24 hours.
24 EBPbeta, C/EBPdelta, KLF4, and Krox20 within hours.
25 ated laminar shear stress for a period of 72 hours.
26 tic lymphoma (SLL) that was maintained at 24 hours.
27 cal ligation and puncture-exposed rats at 24 hours (1.37 +/- 0.2 vs 6.13 +/- 0.3 GPa; p = 0.001) and
28 analyzer range; aspartate aminotransferase 0 hour, 15.6 +/- 9.3 U/L vs 7 hours, 24.8 +/- 14.6 U/L, P
32 - 0.2 vs 6.13 +/- 0.3 GPa; p = 0.001) and 96 hours (5.57 +/- 0.5 vs 6.13 +/- 0.3 GPa; p = 0.006).
33 1 545 634 patients (959 153 fasting >/=10-12 hours; 586 481 nonfasting) from the second harvest of th
34 ligation and puncture-exposed rodents at 96 hours (75.34 +/- 13.2 vs 134.4 +/- 8.2 GPa; p < 0.001).
37 tration of antibiotics (odds ratio, 1.04 per hour; 95% CI, 1.03 to 1.06; P<0.001) but not a longer ti
38 in-hospital mortality (odds ratio, 1.04 per hour; 95% confidence interval [CI], 1.02 to 1.05; P<0.00
39 ho had the 3-hour bundle completed within 12 hours, a longer time to the completion of the bundle was
41 iteria included: no intravenous fluids >/=48 hours, admission >/=14 days of life, congenital heart di
42 trols, including mean number of limbal clock hours affected by OSSN (6 vs 4; P = .12), mean tumor bas
43 ensable for embryonic viability in the first hour after fertilization, but persistently required thro
45 idated proteins that were increased within 1 hour after planned myocardial injury, 29 were also eleva
46 BW significantly increased between the first hour after pulmonary endarterectomy and day 2 (10.2 +/-
48 20 mug/ml (95% CI: 356, 494) were achieved 1 hour after the IV infusion series of 30 mg/kg and 10 mg/
52 c GSK3 inhibitor (L803-mts), starting from 4 hours after 600 mg/kg dose of APAP, resulted in early in
54 demonstrated increased fractional hypoxia 24 hours after angiography and stenting in placebo (+47%) v
55 bility that hypothermia initiated at 6 to 24 hours after birth reduces the risk of death or disabilit
59 tients and occurred after a median time of 3 hours after extracorporeal life support implantation for
60 relationship between oxygenation measured 24 hours after extracorporeal membrane oxygenation onset an
61 herefore be performed ex situ, up to several hours after extraction and storage of the polarized soli
65 nts and in those who survived 24, 48, and 72 hours after injury, as well as at hospital discharge.
68 ravenously with Cyclo/Dox or the vehicle two hours after lights on (zeitgeber time (ZT2), or two hour
71 pm was decreased to 10 ppm between 72 and 96 hours after starting treatment and then to 5 ppm on day
76 al from the reporter gene was detected a few hours after transfection and persisted for 3 days in cel
79 ation to normoxic or ischemic culture for 12 hours, after which viability and function were measured.
81 I<2 ng/L), single cutoff (hs-cTnI<5 ng/L), 1-hour algorithm (hs-cTnI<5 ng/L and 1-hour change<2 ng/L)
82 opean Society of Cardiology recommends a 0/1-hour algorithm for rapid rule-out and rule-in of non-ST-
83 ng/L and 1-hour change<2 ng/L), and the 0/1-hour algorithm recommended in the European Society of Ca
85 important differences in pain reduction at 2 hours among single-dose treatment with ibuprofen and ace
86 t that in the CHAMPION trials reduced the 48-hour and 30-day rates of ischemic events during percutan
89 minuric (urinary albumin excretion <30 mg/24 hours and >300 mg/24 hours, respectively) study group an
97 e met (temperature >/=38 degrees C for >/=12 hours and/or bacteremia) or at day 14 postchallenge.
99 dian time to fixation was 15 hours (IQR 7-24 hours) and delayed fixation was performed in 26% of pati
102 ace of coral skeletons, remain amorphous for hours, and finally, crystallize into aragonite (CaCO3).
103 ificantly from early after reperfusion to 24 hours, and then increases up to day 4, reaching a platea
104 Potential PK/PD predictors included 0- to 24-hour area under the curve (AUC0-24), maximum concentrati
105 on pulmonary edema occurrence in the next 48 hours (area under the receiver-operating characteristics
112 h-related quality-of-life questionnaires, 24-hour blood pressure monitoring, and polysomnography at t
113 verhydration (bioimpedance spectroscopy), 24-hour BP, and left ventricular mass (cardiac magnetic res
118 ne mineral elastic modulus was similar at 24 hours but reduced in cecal ligation and puncture-exposed
120 t-of-hospital cardiac arrest for at least 24 hours, but the optimal duration of TTM is uncertain.
121 g/L), 1-hour algorithm (hs-cTnI<5 ng/L and 1-hour change<2 ng/L), and the 0/1-hour algorithm recommen
124 with an extubation readiness test was 12:15 hours compared with 14:54 hours for extubation without a
126 ned less than 36 degrees C for 92% of the 48 hours cooling period without adverse events, and was low
127 ephalosporin prophylaxis, a postoperative 48-hour course of oral cephalexin and metronidazole, compar
129 al antibiotic administration in the first 24 hours decreased from 5.0% to 2.6% (adjusted difference,
132 using the EHR for a full day of clinic: 2.1 hours during examinations and 1.6 hours outside the clin
133 tacted off-target muscle fibers over several hours during late embryogenesis, with episodic Ca(2+) si
135 uring and -149 mum/hour (IQR, -406 to +1 mum/hour) during interruptions, a statistically significant
136 elocity was +1 mum/hour (IQR, -21 to +49 mum/hour) during posturing and -149 mum/hour (IQR, -406 to +
137 and wind, require scalable, low-cost, multi-hour energy storage solutions in order to be effectively
138 p 5 hours or less; long sleep greater than 8 hours), epigenetic age, naive T cell (CD8+CD45RA+CCR7+),
140 ess test was 12:15 hours compared with 14:54 hours for extubation without an extubation readiness tes
143 hout an IVC filter who survived more than 24 hours from the time of injury, independent of the presen
146 rtality between the 48-hour group and the 24-hour group (hazard ratio, 0.79; 95% CI, 0.54-1.15; P = .
147 ence in the time to mortality between the 48-hour group and the 24-hour group (hazard ratio, 0.79; 95
148 13731 patients who received surgery after 24 hours had a significantly higher risk of 30-day mortalit
156 and alpha1-adrenoceptor expressions within 5 hours in human vascular cells in a nuclear factor-kappaB
157 terrogated DNA methylation at baseline and 3 hours in peripheral blood mononuclear cells (PBMCs) usin
158 ital periods ranging from tens of minutes to hours in which they can accrete gas from their companion
161 lethal chromosomal anomaly, death within 48 hours, inability to determine AKI status or severe conge
162 96-6.42) in those who progressed versus 2.76 hours (interquartile range = 1.60-4.82) in those who did
163 The median time to antimicrobial was 3.77 hours (interquartile range = 1.96-6.42) in those who pro
165 nd mental fatigue (measured by the number of hours into a shift) represent modifiable factors associa
167 n RD border displacement velocity was +1 mum/hour (IQR, -21 to +49 mum/hour) during posturing and -14
168 +49 mum/hour) during posturing and -149 mum/hour (IQR, -406 to +1 mum/hour) during interruptions, a
174 andomized to TTM (33 +/- 1 degrees C) for 48 hours (n = 176) or 24 hours (n = 179), followed by gradu
175 /- 1 degrees C) for 48 hours (n = 176) or 24 hours (n = 179), followed by gradual rewarming of 0.5 de
176 om 30-kg Yorkshire pigs and preserved with 8-hour NEVKP or in 4 degrees C histidine-tryptophan-ketogl
179 release seems to be crucial during the first hour of fermentation, while amylase-mediated sugar relea
181 OS (increase in mean LOS for each additional hour of TTA, 0.06 days; 95% CI, 0.03-0.08 days; P < .001
182 more effective to reduce food intake within hours of administration in overweight, rather than lean,
183 sepsis patients (n = 22 subjects) within 48 hours of admission to the ICU and on days 3 and 7 therea
184 y relevant Gram-negative bacteria within two hours of antibiotic introduction rather than 8-24 h.
185 received an average of approximately 11 more hours of care than white stroke survivors without substa
186 tyle-based interventions offering 52 or more hours of contact showed greater improvements in blood pr
187 vs 8 mm; P = .11), and mean number of clock hours of corneoscleral limbal dissection owing to wide t
188 enile animal, whose ears were fixed within 4 hours of death, revealed that many sensory cells at the
191 lected from children aged <5 years within 24 hours of hospital admission during sentinel surveillance
197 reached target range less than or equal to 4 hours of initiating cooling, remained less than 36 degre
202 e measure was the odds of discharge within 6 hours of presentation There were 11 529 participants in
205 receptor antagonist group during the first 6 hours of sepsis, and there was a significant reduction i
206 Increased MDA levels became evident at 2 hours of slow BD induction at which increased superoxide
207 Of these, 295 (66%) were extubated within 10 hours of starting the extubation readiness test, includi
208 of podoplanin in the IVC increased after 48 hours of stenosis to a substantially higher extent in mi
209 were treated with intravenous tPA within 4.5 hours of symptom onset from 888 surveyed hospitals betwe
212 ly ill patients, greater than or equal to 48 hours on mechanical ventilation with a nonneurologic ICU
215 Milk protein profiles matured within 24 hours or less, indicating the most rapid transition from
216 y awakenings), sleep duration (short sleep 5 hours or less; long sleep greater than 8 hours), epigene
217 y injury) undergoing major surgery lasting 2 hours or longer under general anesthesia were enrolled f
219 ed for noncardiothoracic surgery requiring 2 hours or more of general anesthesia with mechanical vent
222 mphal ticks by measuring metabolism every 24 hours over the course of their up to 96 hour blood meals
226 ion making (mean, 9.70 vs 2.77 instances per hour, P = .03) and failure to progress (mean, 1.20 vs 0.
227 o progress (mean, 1.20 vs 0.13 instances per hour, P = .04) were addressed, and they were more thorou
231 ither a binocular iPad game prescribed for 1 hour per day (n = 40) or patching of the fellow eye pres
237 levels of caspase activity than controls 24 hours post injection, providing biochemical evidence tha
240 in redox regulation were greatly affected 4 hours post-exposure in BAT, while no polar metabolites w
242 d to BoHV-1 infected MDBK cells at 0 and 0.5 hours post-infection, whereas no change was seen when IB
245 tected by cardiac imaging techniques several hours post-PPCI, it may be too late to intervene at that
247 rences were found between preinfusion and 24-hour postinfusion measurements of both T2 (repeated meas
250 Specific natural killer cell depletion 24 hours pre-acute myocardial infarction significantly impr
251 s) or up to 4 automated self-administered 24-hour recalls (ASA24s) over a 1-year period in the women'
252 of arginine were assessed using repeated 24-hour recalls that were administered throughout pregnancy
253 risk = 0.16 [0.06-0.39]; p = 0.0001), and 3 hours (relative risk = 0.09 [0.03-0.27]; p < 0.0001).
254 tive risk = 0.20 [0.09-0.45]; p = 0.0001), 4 hours (relative risk = 0.16 [0.06-0.39]; p = 0.0001), an
255 0.0006), antibiotic administration within 6 hours (relative risk = 0.20 [0.09-0.45]; p = 0.0001), 4
257 min excretion <30 mg/24 hours and >300 mg/24 hours, respectively) study group and 18 healthy voluntee
258 determine whether TTM at 33 degrees C for 48 hours results in better neurologic outcomes compared wit
259 subgroup analysis in early presenters (</=2 hours) revealed significantly lower sensitivity (94.2%,
262 ustment, each 1000-mg difference in usual 24-hour sodium excretion was directly associated with systo
265 ent in power density and durability over 100 hours, surpassing both the baseline Nafion and platinum-
266 scopy (NAP-XPS) we show that a time scale of hours (t>/=4 h) is required for the formation of platinu
267 plus synthetic 2D imaging (38.5 screens per hour) than with FFDM (60 screens per hour) (P < .001).
271 n the highest quartile of use (>558 lifetime hours) to those who were not regular users, the odds rat
272 Z isomer half-lives ranging from seconds to hours, to days and to years, and variable absorption cha
273 ed pluripotent stem cells (iPSCs) after a 72-hour transient incubation in the four chemical inhibitor
274 villin 1 decreased already after a short (3 hours) treatment with necrostatin-1 during renal ischemi
276 In contrast, there was no difference in 24-hour UFC excretion: 6.91 nmol/mmol (SD, 4.67 nmol/mmol)
280 sodium measurement, the use of subsequent 24-hour urine samples resulted in different estimations of
284 number of screening studies interpreted per hour was significantly lower for screening examinations
286 an be monitored simultaneously and flexibly (hours/weeks/months) without the need for restrictive exp
288 lthough neutrophil numbers at baseline and 8 hours were greater in females, the neutrophils were less
289 Temperature data and sunrise and sunset hours were retrieved from Weather Underground, the large
290 ea receptor-1 trajectories between 48 and 72 hours were significantly associated with improved cerebr
292 y (qid) + 1% prednisolone acetate (PA) every hour while awake (q1hWA, Group 1) or qid (Group 2).
294 reparation and analysis time by more than an hour while preserving method accuracy, specificity, and
296 hot (>18 degrees C) and cold (<10 degrees C) hours with wind directions parallel to and perpendicular
298 plasma with maximum concentration around 24 hours, with an apparent half-life of 4 to 5 days and app
300 ls, achieving micromolar precision over many hours without the use of physical barriers or active dri
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