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1 least one definite CCM and 134 were alive at initial presentation.
2 collected and easily obtained at the time of initial presentation.
3 farther from the reference point during its initial presentation.
4 time of phlebotomy, on average 4 hours from initial presentation.
5 to clinical deterioration 7 to 10 days after initial presentation.
6 e stimulus that had lasted longer during its initial presentation.
7 nd recurrent ACS were assessed 30 days after initial presentation.
8 ce rate for ABS was 11.4% over 4 years after initial presentation.
9 remained free of tumor for 5 years after the initial presentation.
10 ity to or with the same localizations as the initial presentation.
11 P) had been considered in all three cases at initial presentation.
12 tion who had cTnI assay drawn at the time of initial presentation.
13 8%) completed a questionnaire 3 months after initial presentation.
14 patients had positive CMV IgG serologies at initial presentation.
15 chest radiographs and CT images available at initial presentation.
16 ed a simplified fast-track screen for use at initial presentation.
17 lood specimens obtained from all patients at initial presentation.
18 ity vasculitis on the basis of the patients' initial presentation.
19 ay in resuscitation, or laboratory values on initial presentation.
20 s, leukemia cutis, or meningeal leukemia) at initial presentation.
21 atient with angiographically-confirmed PE at initial presentation.
22 ropriately evaluated and managed after their initial presentation.
23 sually affected the same organ systems as on initial presentation.
24 he left hip was performed 4 months after the initial presentation.
25 gery at a mean duration of 18.1 months after initial presentation.
26 vitreal vancomycin-ceftazidime injections at initial presentation.
27 ontrast material approximately 8 hours after initial presentation.
28 male: 249/53) with CSC were evaluated on the initial presentation.
29 MRI (Fig 3) was performed 2 months after the initial presentation.
30 c spine MRI was performed 2 months after the initial presentation.
31 but infection presence is often uncertain at initial presentation.
32 rs at disease onset and 9.3 years at time of initial presentation.
33 en when treatment is within a few days after initial presentation.
34 ens, and clinical outcomes 14 days after the initial presentation.
35 ancreatic function, with varying severity of initial presentation.
36 cording to persisting symptoms as opposed to initial presentation.
37 antation occurred in 13% within 2 decades of initial presentation.
38 ative CT images of 364 EOC patients at their initial presentation.
39 5 years, and depression is the most frequent initial presentation.
40 jority of eyes with iERM remain stable after initial presentation.
41 which was similar in severity compared with initial presentation.
42 ch was similar in severity compared with the initial presentation.
43 ere classified as non-metastatic (M0) at the initial presentation.
44 ent, if the latter were within 14 days after initial presentation.
45 factors that predispose to persistent AF on initial presentation.
46 me) in STEC-infected children without HUS at initial presentation.
47 morrhagic and nonhemorrhagic groups based on initial presentation.
48 odies (ANA) and ANA subsets were obtained at initial presentation.
49 ve disease persisting more than 90 days from initial presentation.
50 peat ED visits and hospital admissions after initial presentation.
51 penia, and hyponatremia were often absent at initial presentation.
52 after stabilization and again 30 days after initial presentation.
53 ecurrence are linked to the primary tumor at initial presentation.
54 pathogen-related differences in symptoms at initial presentation.
55 rological symptoms have been described after initial presentation.
56 ies were obtained 3 months and 4 years after initial presentation.
57 efined epitopes approximately 2 months after initial presentation.
58 case of PALG with hyperopic shift and CFs as initial presentation.
59 d for device activation within 90 minutes of initial presentation.
60 l discriminations for repeated compared with initial presentations.
61 gnostic uncertainty at the time of patients' initial presentations.
62 d platelet counts are relatively uncommon in initial presentations.
63 eturn to the ED for AF within 30 days of the initial presentation (1.6% to 2.7%; hazard ratio, 1.70 [
67 52%] female) aged 2 to 18 years (mean age at initial presentation, 28 months; range, 0-121 months) we
68 .5); P = 0.041] and altered consciousness at initial presentation [3.0 (1.3-6.7); P = 0.0077] were as
69 37.5%, P = 0.061), have liver failure at the initial presentation (37.8% versus 9.3%, P = 0.001), and
73 , most patients improved within 1-2 weeks of initial presentation after vaping cessation and administ
75 The age and gender of each participant upon initial presentation, along with biological parameters,
76 vided to sepsis and septic shock patients at initial presentation and 2) determine the association be
77 (TCR) repertoire in aplastic anemia (AA) at initial presentation and after immunosuppression using a
79 therapy (ECT) on two separate occasions: on initial presentation and again a year later when the pat
82 gH CDRII region was identical at the time of initial presentation and at relapse suggesting that clon
83 who did not have bone marrow involvement at initial presentation and at time of the procedure, albei
84 potency of these responses in patients upon initial presentation and before treatment, we determined
85 ion and level of evidence in the approach to initial presentation and diagnosis of NSTE-ACS, risk ass
90 is of anterior uveitis within 90 days before initial presentation and had follow-up visits thereafter
91 asciitis is often confused for cellulitis at initial presentation and is considered to be more severe
92 ic yield and corrected visual acuity (VA) at initial presentation and last follow-up (up to 1 year) w
94 ion of repeating the RPR titer if the day of initial presentation and the day of treatment are differ
95 ho underwent syphilis serology on the day of initial presentation and the day of treatment, if the la
96 nitoring was significantly influenced by the initial presentation and the distribution of blood obser
99 come of the consecutive NAION event based on initial presentation and to compare mean visual loss of
100 in RPR titer, stratified by the time between initial presentation and treatment and by syphilis stage
101 syphilis cases, the median duration between initial presentation and treatment was 6 days (interquar
102 titer increased with increasing time between initial presentation and treatment, from 5.7% (n = 6) 1-
103 collected and analyzed information regarding initial presentations and final outcomes in patients dia
104 as to analyze the characteristic features of initial presentations and final outcomes of PPLA caused
105 centage of questions answered correctly upon initial presentation) and completion scores (percentage
106 233 (86.1%) were transferred the same day as initial presentation, and 1897 (73.2%) received antibiot
107 d conditions, complicated biliary disease on initial presentation, and initial presentation to the em
108 psies of test cohorts was performed at their initial presentation, and those spontaneously eliminatin
109 ith AIH, have more aggressive disease at the initial presentation, are less likely to respond to conv
111 istologic examination and wound culture from initial presentation as well as clinical follow-up docum
112 ent, we used data available during patients' initial presentation at the emergency department (ED) to
113 osed with definite IE within the 12 weeks of initial presentation based on modified Duke criteria.
114 iagnosed with definite IE within 12 weeks of initial presentation based on modified Duke's criteria.
115 ) had cochleovestibular dysfunction as their initial presentation before rhombencephalitis/encephalom
116 ference in glaucoma or suspect prevalence at initial presentation between eyes treated with injection
117 a history of RT or RRD in the fellow eye at initial presentation but only 0.7% of patients without a
121 Several clinical variables at the time of initial presentation can predict the future risk of deta
122 in patients with lacrimal involvement as the initial presentation, can be difficult because of nonspe
123 patients at risk for malnutrition regarding initial presentation, clinical outcomes, and treatment r
124 e weakness (50%) and muscle atrophy (67%) at initial presentation compared with antisynthetase-positi
125 t an immunodeficiency with a clinically mild initial presentation could be a combined immunodeficienc
127 tients, 13 (26%) were correctly diagnosed at initial presentation; diagnosis was delayed, on average,
129 ascular conditions among patients with AN at initial presentation, during treatment, and at follow-up
130 record review (length of symptoms; times of initial presentation, emergency department (ED) triage,
131 ht, gestational age at birth, bicarbonate at initial presentation, feeding type, preoperative duratio
134 pect to tumor grade, prevalence of necrosis, initial presentation, final margins, and receipt of endo
136 ed several but not all of her NHPs after her initial presentation for acute hepatitis at the first in
142 Patients with typical AD and non-amnesic initial presentation had a significantly higher ratio of
143 ion of that shape, regardless of whether its initial presentation had been supraliminal or subliminal
144 distant-stage (metastatic) breast cancer at initial presentation has increased significantly in U.S.
145 and severity of heart failure at the time of initial presentation have been formally categorized by t
148 Extra-adrenal oligometastatic disease at initial presentation (HR: 1.84, P = 0.016), larger tumor
149 d as quiescence of disease within 90 days of initial presentation, HZO recurrence was defined as any
150 art tuberculosis treatment within 2 weeks of initial presentation if all required consumables were av
156 5P mutation during vitreous biopsy or at the initial presentation in the clinic if vitreous biopsy wa
160 ed glaucoma screening efforts, since delayed initial presentation is a major risk factor for vision l
162 es, along with a high degree of suspicion on initial presentation is crucial in order to provide the
163 cess but the detection of CTC at the time of initial presentation is not necessarily a poor prognosti
164 insufficiency is usually delayed because the initial presentation is often non-specific; physician aw
165 We found medium concordance for testing at initial presentation (k = 0.68) and very low concordance
166 proliferation caused by its multifocality at initial presentation, lack of aneuploidy, and spontaneou
167 ection of the primary sites months after the initial presentation, light microscopy, and comprehensiv
168 festations may develop many months after the initial presentation, mandating the need for long-term f
169 ) and to describe to what extent a patient's initial presentation may be predictive of encephalitis e
170 at the final visit after treatment than the initial presentation (median CMT 332,5u versus 234u, p <
174 ing a multivariate analysis, was symptoms at initial presentation (odds ratio [95% confidence interva
175 mTBI with complete 30-day data and a median initial presentation of 90 minutes after injury, those w
176 f a pre-existing neurological condition, the initial presentation of a non-pregnancy-related problem,
177 stigate a pattern of association between the initial presentation of a patient and the etiologic path
178 A 2-year lookback period from the date of initial presentation of AACC was used to identify patien
179 basis of nonischemic FFR in patients with an initial presentation of ACS is associated with significa
182 of FA is likely facilitated by the improper initial presentation of antigen to the developing immune
183 ciation between a panel of blood proteins at initial presentation of bacteremia and disease severity
184 compared cumulative incidence curves for the initial presentation of cardiovascular disease and used
185 fluid samples collected from children during initial presentation of central nervous system inflammat
186 vationProcedure: Baseline characteristics at initial presentation of children with PCG in the registr
192 litis optica (NMO) IgG seropositivity at the initial presentation of longitudinally extensive transve
195 time between exposure to gadolinium and the initial presentation of NSF is typically weeks to months
198 nal detachment cases with primary PVR at the initial presentation of RD were more likely to undergo s
202 autoimmune diseases are characterized by the initial presentation of the disease being the most sever
203 without neurological involvement) either as initial presentation of the disease or as relapse are un
204 symptoms are not only common, but may be the initial presentation of this systemic inflammatory proce
205 asmatic tuberculomas were not present at the initial presentation of tuberculosis and appeared on bra
214 rectly related to the underlying malignancy (initial presentation or progressive disease), to its tre
215 96 [95% CI, 0.61-1.52]) or at 3 months after initial presentation (OR, 1.26 [95% CI, 0.78-2.04]).
216 tudied, 36 (22%) had TE disease confirmed at initial presentation (PE = 19; DVT only = 17), and four
217 tation (when available), patient symptoms at initial presentation, physical examination findings, ana
219 h severe COVID-19 and sBSI had a more severe initial presentation, prolonged hospital course, and wor
222 Five athletes (7.2%) considered normal on initial presentation subsequently expressed pathology du
223 rmal, 16 patients; LOH, 2 patients) as their initial presentation, suggesting, albeit with a small pa
231 treatment, from 5.7% (n = 6) 1-3 days after initial presentation to 26.2% (n = 27) at 10-14 days (Pt
232 presentation without abrupt or any pain, and initial presentation to a nontertiary care hospital (all
234 and blood panel profile data at the time of initial presentation to develop machine learning algorit
235 were offered a full 28-day course of PEP at initial presentation to healthcare, with fewer refusals
236 evere injuries is positively associated with initial presentation to high-volume trauma hospitals.
237 ents with systemic vasculitis increased from initial presentation to last observation by a median sco
239 re is recommended for at least 72 hours from initial presentation to maximize the potential for recov
241 se-induced leg pain questionnaire, time from initial presentation to surgery, and whether a patient h
243 unger (nonelderly) patients with COVID-19 at initial presentation to the emergency department (ED); o
246 ing outcomes at 24 and 72 h from the time of initial presentation to the emergency room, and it provi
249 s with chronic lymphocytic leukemia (CLL) at initial presentation to University of Texas M.D. Anderso
250 astatic) were unrelated to clinical stage at initial presentation, treatment history, or histopatholo
251 f DSS included distant metastasis at time of initial presentation; venous, capsular, and adjacent org
254 tance Best corrected visual acuity (BCVA) at initial presentation was 0.36 +/- 0.29logMAR and at last
256 et was 8.2 (3.6) years, the mean (SD) age at initial presentation was 10.4 (3.6) years, and 66 (55.5%
257 the adjusted hazard ratio for haemorrhage at initial presentation was 13.9 (95% CI 2.6-73.8; p=0.002)
259 al visit, a high degree of vitreous cells at initial presentation was associated with a lower inciden
263 Focusing on the variables that describe the initial presentation, we performed a factor analysis of
265 3 with inflammatory-distributive features at initial presentation were excluded, leading to a cohort
267 medical records and SD-OCT images at time of initial presentation were reviewed in patients with biop
268 ermore, different potentials recorded during initial presentations were indicative of perceptual lear
270 e patients were studied 30 years after their initial presentation with a clinically isolated syndrome
274 blast cells from 104 consecutive children at initial presentation with acute lymphoblastic leukemia (
275 rs; OR, 6.38; 95% CI, 1.35-30.16; P = .009), initial presentation with bilateral ocular involvement (
276 ospectively followed cohort of children from initial presentation with either multiple sclerosis or m
279 acco use [1.40 (1.18-1.66)]; and complicated initial presentation with obstruction [1.33 (1.06-1.65)]
280 Given the early onset of symptoms and the initial presentation with pulmonary embolism in some fam
281 ive protein (hs-CRP), for risk assessment at initial presentation with ST-segment elevation myocardia
282 apid plasma reagin (RPR) titer on the day of initial presentation with that on the day of syphilis tr