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1 , 16.2 versus 6.8 years before the estimated symptom onset).
2 the latest time interval tested (>20 d after symptom onset).
3 age diagnostic delay is up to 5-6 years from symptom onset.
4 g severity who presented within a week after symptom onset.
5 lymerase chain reaction (PCR) >30 days after symptom onset.
6 less than 1% of transmission occurred before symptom onset.
7 oxygen support, at a median of 25 days after symptom onset.
8 ive procedures and when performed soon after symptom onset.
9 e optimal time window of the treatment after symptom onset.
10 virus 2 infection, grouped by interval since symptom onset.
11 alse-negative rate by day since exposure and symptom onset.
12 ith receiving treatment within 24 hours from symptom onset.
13 by orders of magnitude within a few days of symptom onset.
14 r to 30% of infected cases within 48 h after symptom onset.
15 nterpretation of the test, such as time from symptom onset.
16 ng patients with lesion age < 4.5 hours from symptom onset.
17 birth has been correlated to patient age at symptom onset.
18 ndings peaked at 10-12 days from the date of symptom onset.
19 en treatment was started within 7 days after symptom onset.
20 nd genetic factors associated with period of symptom onset.
21 ementia Rating scores and estimated years to symptom onset.
22 the semen of the survivors after 9 months of symptom onset.
23 early as their 30s, decades before expected symptom onset.
24 om respiratory failure within 3-5 years from symptom onset.
25 onsolidation which peaked at 10-12 days from symptom onset.
26 0.13) using samples collected >14 days after symptom onset.
27 or treatment delayed as long as 3 days after symptom onset.
28 n-QW despite treatment within 12 hours after symptom onset.
29 iverge already at 17.8 years before expected symptom onset.
30 rapeutic disease-modifying time window after symptom onset.
31 rwent follow-up unenhanced CT 24 hours after symptom onset.
32 .5%) of patients presented within 2 weeks of symptom onset.
33 r first medical help later than 30 min after symptom onset.
34 d involvement of the fellow eye 1 year after symptom onset.
35 nd stroke mimics (n = 20) within 24 hours of symptom onset.
36 before development of TBM-IRIS through IRIS symptom onset.
37 ntion and presenting less than 12 hours from symptom onset.
38 favorably in patients presenting early after symptom onset.
39 s had IVT started within 4.5 hours of stroke symptom onset.
40 or endovascular therapy up to 18 hours after symptom onset.
41 l delay in the one individual treated before symptom onset.
42 to NCs, starting 11.2 years before expected symptom onset.
43 ells) or placebo between 24 h and 48 h after symptom onset.
44 for days 2-90, given orally) within 24 h of symptom onset.
45 in spinal MNs of TDP-43-driven ALS at motor symptom onset.
46 ATXN1 mRNA by rAAV.miS1 when delivered after symptom onset.
47 by stroke specialists within 24 hours after symptom onset.
48 everse disease readouts when delivered after symptom onset.
49 ated with increased WMH well before expected symptom onset.
50 crease approximately 6 years before expected symptom onset.
51 controls, more than 15 years before expected symptom onset.
52 rresponds to the second and third week after symptom onset.
53 ion corresponding to day 10 (IQR 8-12) after symptom onset.
54 se with atrophy and hypometabolism closer to symptom onset.
55 carriers (preHD) far from predicted clinical symptom onset.
56 ayed, i.e., 3 days or longer) with regard to symptom onset.
57 reshold (Ct) value was >30 or >14 days after symptom onset.
58 f the first positive nucleic acid test after symptom onset.
59 sitivity to >80% between days 6 and 10 after symptom onset.
60 ission between 0.5 and 8.0 hours after known symptom onset.
61 e viral load-time AUC lies within 10 days of symptom onset.
62 able among persons tested up to 90 days post symptom onset.
63 two individuals, most prominently the age of symptom onset.
64 S-CoV-2 spike protein at least 2 weeks after symptom onset.
65 on-carriers from 16 years prior to estimated symptom onset.
66 % CI, 85.0%-98.3%) for samples >14 days post symptom onset.
67 ues <26) and were obtained within 21 days of symptom onset.
68 oV-2-specific serum IgA and IgG titers after symptom onset.
69 d using samples collected 7 to 14 days after symptom onset.
70 2.5 or 3.5 and with more transmission before symptom onset.
71 ative or became positive 12 to 14 days after symptom onset.
72 olds (Ct) occurring 9, 26, and 36 days after symptom onset.
73 patients were enrolled within 12 hours from symptoms onset.
74 proved to be predictive of postoperative DED symptoms onset.
75 ive and at least two weeks have passed since symptom onset; 2) assessment of multisystem inflammatory
77 t one symptom after a mean of 125 days after symptoms onset, 33.3% reported one or two symptoms and 1
78 as started within a median of 285 minutes of symptom onset; 51 (41%) patients achieved a mTICI 2b, an
79 ts had abnormal MRI findings 2-4 weeks after symptom onset (58.9%), including 17 with acute ischemic
80 al sensitivity during the first 5 days after symptom onset, 70%-71% from Days 9 to 11, and 30% at Day
83 eceived medical help later than 30 min after symptom onset, adrenaline auto-injector prescription is
86 ve cohort study, we collected data on age at symptom onset, age at death, and disease duration for pa
87 es by doing an international study of age at symptom onset, age at death, and disease duration in ind
88 the upper airway prior to or at the time of symptom onset, an unusual feature that has enabled wides
89 19.8 days +/- 6.1 (95% CI: 18.1, 20.2) after symptom onset and 10.5 days +/- 3.8 (95% CI: 10.2, 12.9)
91 ample mean (SD) age was 64.1 (10.3) years at symptom onset and 67.9 (9.9) years at Three Words Three
92 trol for confounders: age, sex, time between symptom onset and admission <= 7 days, Charlson comorbid
93 for sex, the TBI+ bvFTD group had an age of symptom onset and age of diagnosis that was on average 2
97 ittsburgh compound B PET, estimated years to symptom onset and Clinical Dementia Rating Scale-Sum of
99 Infectiousness peaks around a day before symptom onset and declines within a week of symptom onse
101 y (TBI) is associated with an earlier age of symptom onset and diagnosis in a large sample of patient
102 agnosis is associated with an earlier age of symptom onset and diagnosis in patients with bvFTD.
104 nk in the stroke rescue chain, starting with symptom onset and ending with recanalisation, should be
106 time-dependent local immune responses before symptom onset and explaining the as-yet unpredictable ou
107 In CRVO patients, even minor delays between symptom onset and first injection led to less optimistic
108 vidual progressive phenotypes than on age at symptom onset and for clinical trials will help optimize
110 s and related products in the 90 days before symptom onset and had pulmonary infiltrates on imaging a
111 antigens in 95% of patients by 4 weeks after symptom onset and IgG to the RBD increased until the thi
112 pa = 0.78) after greater than 1 hour between symptom onset and imaging, which increased to high agree
114 neurofilament-heavy chain) are normal before symptom onset and increased by at least an order of magn
117 nal analysis at baseline showed that earlier symptom onset and longer duration since onset was associ
118 on of gamma-MNs in SOD1(G93A) mutants delays symptom onset and prolongs lifespan, demonstrating a pat
120 nd IgG antibodies in 5-d time intervals from symptom onset and studied the specificity of each assay
121 level data regarding infectiousness prior to symptom onset and the asymptomatic proportion among all
123 serum samples collected 6 or more days after symptom onset (and the immunoglobulins M and G in all 33
124 patients with acute NAION (within 14 days of symptom onset) and 15 control patients with age-related
125 a expansion, all occurring within 48 h after symptom onset) and five (19%) of 27 in the PCC group (no
126 33 samples collected at least 15 days after symptom onset), and correctly classified 456 out of the
127 In this retrospective study, we examined symptom onset, and genetic and neuropathological data fr
129 symptom onset and declines within a week of symptom onset, and no late linked transmissions (after a
130 rrelation between IgG avidity and days since symptom onset, and peak readings were significantly high
131 tandem with immunoglobulin titers following symptom onset, and positive percent agreement between de
132 proportion seeking treatment within 1 day of symptom onset, and presence of primary proliferative vit
133 relationships of baseline Q waves, time from symptom onset, and reperfusion strategy with in-hospital
135 portion of transmission that occurred before symptom onset, and the proportion of subclinical infecti
136 .7%) cases likely transmitted TB well before symptom onset, and these were largely sputum negative at
137 as age of onset younger than 65 years, rapid symptom onset, and/or impairment in multiple cognitive d
140 tures, investigated associations with age at symptom onset, APOE genotype, and mutation position, and
141 fection when measured at least 14 days after symptom onset, are associated with clinical severity, an
143 of pathology with group, estimated years to symptom onset, as well as cross-modal relationships.
144 t 90 days in patients enrolled within 3 h of symptom onset, assessed in the intention-to-treat popula
146 he age period of self-reported atopic eczema symptom onset based on repeated measures of self-reporte
147 with 2 reported incidents of pertussis with symptom onset between 1 January 2010 and 31 December 201
148 ively, when performed 14 days or later after symptom onset, but sensitivity decreased at earlier time
150 MR was performed within the first week after symptom onset (CMR-I) and repeated after 6 months (CMR-I
151 ificant difference was observed in age, sex, symptom onset, comorbidities, tumor history, use of resp
152 , an R(0) of 1.5, and 0% transmission before symptom onset could be controlled even with low contact
154 days of infection before the typical time of symptom onset (day 5), the probability of a false-negati
155 early oseltamivir treatment (<=48 hours from symptom onset) decreases mortality compared to late trea
156 uding site of onset (bulbar or limb), age at symptom onset, delay from onset to diagnosis and the use
160 clinical data available on sex, age at motor symptom onset, disease duration (from motor symptom onse
162 rmed COVID-19 cases sampled at >14 days post-symptom onset (DPSO), whereas the salivary anti-receptor
163 ipants with COVID-19 symptoms (<=7 days from symptom onset [DSO], >=18 years of age) were utilized to
165 focal dystonia evaluated within 5 years from symptom onset, enrolled in the Natural History Project o
167 rofilament light and estimated years to/from symptom onset (EYO), as well as years to/from actual ons
168 PINK1, LRRK2 and SNCA in relation to age at symptom onset, family history and clinical features.
170 ool specimens collected within 7 days of AGE symptom onset for clinician-requested diagnostic testing
171 ore, current strategies that rely solely on "symptom onset" for infection identification need urgent
172 ted with intravenous tPA within 4.5 hours of symptom onset from 888 surveyed hospitals between June 2
173 onance at 1.5 T seven days (5-10 days) after symptom onset (FU0), after 5 weeks (FU1), and after 6 mo
174 ICP at 9-15 weeks of gestation and prior to symptom onset (group 1 cases/samples: ICP n = 35/80, unc
176 d neurological onset earlier after prodromal symptom onset, had milder weakness, showed more rapid im
177 associated with less years before estimated symptom onset, higher global Abeta brain burden, and wit
179 ithin 12 hours and again at 48+/-24 hours of symptom onset in 172 patients with imaging-confirmed AIS
180 used chart-confirmed cases with adjudicated symptom onset in a self-controlled risk interval (SCRI)
182 l interval (SI), defined as the time between symptom onset in an infector and infectee pair, is commo
184 d by at least an order of magnitude at early symptom onset in CSF (pNF-H) or serum and CSF (NF-L).
186 s closer to and beyond their expected age of symptom onset in key frontotemporal dementia signature r
188 thrombolysis (alteplase bolus) within 3 h of symptom onset in North America and within 4.5 h of sympt
189 VID-19 cases could have been detected before symptom onset in real time via a two-tiered warning syst
190 s also altered in vivo in spinal cord before symptom onset in SBMA mice, and crucially in motor neuro
192 m onset in the risk interval and 51 cases of symptom onset in the control interval were identified.
195 patients were assigned within 24 hours after symptom onset, in a 1:1 ratio, to receive a 30-day regim
196 , acquired at a mean of 11 +/- 10 days after symptom onset, in addition to follow-up scans of 16 pati
197 ic medication use, on AR symptoms and asthma symptoms/onset, in patients with birch pollen-associated
198 alysed genotypic and phenotypic data (age at symptom onset, initial cognitive or behavioural symptoms
199 cation, head CT performed within 72 hours of symptom onset, initial DS angiographic results negative
202 period between immunization and EAE's overt symptom onset is characterized by distinct host response
204 les well-informed prospective studies, since symptom onset is near certain and age of onset is predic
205 roup analysis, treatment within 7 days after symptom onset led to lower 90-day mortality than use of
206 tures associated with early-onset PE (EO-PE; symptom onset < 34 weeks) and late-onset PE (LO-PE; symp
207 domly assigned patients (1:1:1 stratified by symptom onset </=4 days or 5-6 days) to receive 300 mg o
208 levation myocardial infarction within 6 h of symptom onset (<2 h, n = 107; >=2 h but <4 h, n = 235; >
209 cation of independent predictors of risk for symptom onset may guide education and clinical managemen
210 X levels were associated with earlier age of symptom onset (median ePPIX levels for those who develop
211 sented to the hospital within 24 hours after symptom onset (median time from symptom onset to blood s
212 C allele was associated with a higher age at symptom onset (median years A/A 63.5, A/C 65.6, and C/C
214 sign) was a good predictor of ocular surface symptom onset (odds ratio, 9.45; 95% confidence interval
216 predict progression from normal cognition to symptom onset of mild cognitive impairment or dementia:
218 rum samples collected more than 14 days post-symptom onset or post-initial positive reverse transcrip
219 Serum and urine collected within 4 weeks of symptom onset or within 6 weeks of travel were tested wi
221 point prevalence of SARS-CoV-2 and assessed symptom onset over 30-day follow-up to determine: (1) th
225 wenty-two of those patients (78.6%) reported symptom onset prior to or in conjunction with the molecu
226 measures become abnormal around the time of symptom onset, prior to diagnosis, and may be of value f
227 both IgG and IgM occurs around 12 days post-symptom onset (range 1-40), with extensive individual va
229 bitor of extracellular PPIA, MM218, given at symptom onset, rescued motor neurons and extended surviv
231 edian time to baseline visit, 358 days after symptom onset), six symptoms were reported significantly
232 hat TB transmission can occur before patient symptom onset, suggesting also that TB transmits during
234 levels potentially increasing just prior to symptom onset, suggesting that GFAP may be an important
235 ismatch profile treated up to 18 hours after symptom onset supports a randomized trial of endovascula
238 20% (CI, 12% to 30%) on day 8 (3 days after symptom onset) then began to increase again, from 21% (C
240 Of the area under the curve (AUC) spanning symptom onset to 30 days, 96.9% lay within the first 7 d
241 n probabilities increase from roughly 10% at symptom onset to 98-100% by day 22, after which IgM wane
243 the test varies with time from exposure and symptom onset to avoid being falsely reassured by negati
244 hours after symptom onset (median time from symptom onset to blood sampling = 3.3 hours; interquarti
246 Ischemic time, defined as the time from symptom onset to coronary reperfusion, was a pre-specifi
248 symptom onset, disease duration (from motor symptom onset to death or to the date of censoring, Dec
249 Shorter disease duration from cognitive symptom onset to death was observed in men (beta, -0.73;
250 60.9 years (IQR 52.7-68.2), median time from symptom onset to diagnosis was 1.01 years (IQR 0.67-1.67
252 SARS-CoV-2 infection, with an interval from symptom onset to enrolment of 12 days or less, oxygen sa
255 significant difference in the duration from symptom onset to groin puncture (254 minutes for the IVT
257 y of control decreases with long delays from symptom onset to isolation, fewer cases ascertained by c
258 c reproduction number (R(0)), the delay from symptom onset to isolation, the probability that contact
259 versus 10.0%), consistent across times from symptom onset to presentation (15.4% versus 9.9% </=3 ho
260 5 years [SD, 13.1]; women, 47.0%), time from symptom onset to randomization was 196 minutes (IQR, 142
262 lts In the stent retriever arm of the study, symptom onset to reperfusion time of 150 minutes led to
263 scenario analyses, we varied the delay from symptom onset to self-isolation, the proportion of sympt
264 eshold (Ct) values from respiratory samples, symptom onset to test (STT), and infectivity in cell cul
265 demonstrate a significantly longer time from symptoms onset to hospital admission among patients with
267 l 1) in 2018 and 2019, in terms of time from symptoms onset to hospital admission, clinical character
270 tery were included less than 4.5 hours after symptom onset using standard intravenous thrombolysis el
279 Treatment with BAT product at <=2 days of symptom onset was associated with shorter hospital and I
280 he association of viral load with days since symptom onset was examined in a multivariable regression
282 ymptoms (>40 years); the mean age for asthma symptoms onset was 30.2 years and for asthma diagnosis 3
283 T-confirmed acute ICH scanned within 48 h of symptom onset, we investigated the sensitivity and speci
286 ic stroke who could be treated within 8 h of symptom onset were randomly assigned to medical therapy
288 had CT angiography within 6 and 12 hours of symptom onset, were categorized according to the occlusi
289 ed from 2 days to a maximum of 6 weeks after symptom onset, whereas Mp DNA and antibodies persisted u
290 These plaques form 10-20 years before AD symptom onset, whereas robust tau pathology is more clos
291 nfirmed cases with identifiable exposure and symptom onset windows to estimate the incubation period
292 logical sensitivity increased with days post symptom onset with >50% of patients seropositive by at l
293 sensitivity of PCR decreased with days post symptom onset with >90% clinical sensitivity during the
294 ntiating between ICH and IS within 4.5hrs of symptom onset with a sensitivity of 61% and a specificit
295 information, 22 were detected before (or at) symptom onset, with four cases detected at least nine da
296 % CI, 81.8%-96.7%) for samples >14 days post symptom onset, with specificity 94.4% (95% CI, 89.2%-97.
297 water uptake identifies stroke patients with symptom onset within 4.5 hours with high accuracy and ma
298 drome coronavirus 2 infection, with COVID-19 symptom onset within 7 days and oxygen saturation of 92%
299 and further characterise subtypes by time of symptom onset within pregnancy and three post-partum per
300 Self-isolation by 20% of cases 24 h after symptom onset would delay and flatten the outbreak traje