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1 Auditory Serial Addition Test-3 [PASAT], and Expanded Disability Status Scale).
2 r correlated with disability measured on the Expanded Disability Status Scale.
3 ing-remitting MS and mild disability (EDSS - Expanded Disability Status Scale 1-3.5) and 16 control s
4 ntion-to-treat analysis of time to 1- (entry expanded disability status scale, 3.0-5.0) or 0.5-point
5 panded disability status scale change (entry expanded disability status scale, 5.5-6.5) sustained for
6 Furthermore, 50% of CD24v/v patients with expanded disability status scale 6.0 reached the milesto
7 Clinical disability was measured with the Expanded Disability Status Scale, 9-Hole Peg Test, and 2
8 r 3 months confirmed 1-point increase on the Expanded Disability Status Scale), active magnetic reson
9 ndary endpoints were disability (measured by expanded disability status scale), ambulation (Hauser sc
10 weeks with validated measures of impairment (Expanded Disability Status Scale and Functional Systems)
12 of GM change with clinical outcome measures (Expanded Disability Status Scale and Multiple Sclerosis
13 patients and correlated positively with the Expanded Disability Status Scale at attack leading to bi
17 uation included motor and cognitive testing: Expanded Disability Status Scale, cerebellar Functional
18 sability status scale, 3.0-5.0) or 0.5-point expanded disability status scale change (entry expanded
19 d with higher disability, as assessed by the Expanded Disability Status Scale (coefficient = -0.41, 0
20 days with no measurable improvement) on the Expanded Disability Status Scale (EDSS) (range, 0-10, wi
21 tures including presenting symptoms, time to Expanded Disability Status Scale (EDSS) 4.0, 6.0 and 8.0
22 ability milestones was shorter than in ROMS (Expanded Disability Status Scale (EDSS) 4.0:8.1 vs. 17.1
23 Physical disability was assessed using the expanded disability status scale (EDSS) and motor compon
24 nds only and disability determined using the Expanded Disability Status Scale (EDSS) and Multiple Scl
25 rological examination and were scored on the Expanded Disability Status Scale (EDSS) and Multiple Scl
28 linical and laboratory data including serial Expanded Disability Status Scale (EDSS) assessments, fro
30 ute T2 lesion volume and either the absolute expanded disability status scale (EDSS) grade (P = .32)
31 ed relapse rate, number of relapses, time to Expanded Disability Status Scale (EDSS) progression, cha
32 d, or natalizumab), age 65 years or younger, Expanded Disability Status Scale (EDSS) score 6.5 or low
33 he intragroup relationship between WBNAA and Expanded Disability Status Scale (EDSS) score and Mann-W
34 atio (treated vs untreated) measured both in Expanded Disability Status Scale (EDSS) score and utilit
35 value and the variation from baseline of the Expanded Disability Status Scale (EDSS) score at 60 mont
36 gative correlation between brain atrophy and Expanded Disability Status Scale (EDSS) score in patient
37 efinite MS, CDMS (second attack or sustained Expanded Disability Status Scale (EDSS) score increase))
38 e participants were aged 18-55 years, had an Expanded Disability Status Scale (EDSS) score of 0-5.0,
39 sion of disability measured by change in the Expanded Disability Status Scale (EDSS) score of 1.0 or
40 t no relapse in the previous 30 days, and an Expanded Disability Status Scale (EDSS) score of 5.5 poi
41 r MS onset took the longest time to reach an Expanded Disability Status Scale (EDSS) score of 6 (mean
42 ubcutaneous interferon beta-1a, and the mean expanded disability status scale (EDSS) score of the ale
44 g no relapse, no 3-month sustained change in expanded disability status scale (EDSS) score, and no ne
45 andomisation sequence, balanced according to expanded disability status scale (EDSS) score, centre, a
46 tients; 3.81 [0.13-9.47]; p=0.032), although expanded disability status scale (EDSS) scores were not
50 nt, neurologic disability as measured by the Expanded Disability Status Scale (EDSS) was stable or im
51 for early disease activity predicting severe Expanded Disability Status Scale (EDSS) worsening (worst
52 te endpoint based on change from baseline in Expanded Disability Status Scale (EDSS), 25' Timed-Walk
53 1.5 T scanner and clinically assessed on the Expanded Disability Status Scale (EDSS), 9-hole peg test
54 improved by at least 1 point on the Kurtzke expanded disability status scale (EDSS), and five patien
55 d moderate or severe locomotor disabilities [Expanded Disability Status Scale (EDSS), score 3.5-8], w
56 monly used scales in multiple sclerosis, the Expanded Disability Status Scale (EDSS), the Scripps Neu
58 d DMD exposure decreased the risk of a first Expanded Disability Status Scale (EDSS)-worsening event
65 r) between imaging data and clinical scores (Expanded Disability Status Scale [EDSS] and MS multiple
66 ated with disability (as determined with the Expanded Disability Status Scale [EDSS] score; P = .046,
67 at was constrained by experimental data (the expanded disability status scale [EDSS] time series) obt
68 associated with clinical (conversion to MS, Expanded Disability Status Scale [EDSS]) and magnetic re
71 evolution (-0.23 points annually; P = .01), Expanded Disability Status Scale evolution (0.57 points
72 sociated clinical data was used to calculate expanded disability status scale for each patient preced
75 included: history, neurological examination, expanded disability status scale, magnetic resonance ima
76 7.2 +/- 15 months; RRMS: 8.0 +/- 6.5 years, Expanded Disability Status Scale (median, min-max): CIS:
78 e or relapsing-remitting multiple sclerosis (Expanded Disability Status Scale: median = 1, range = 0-
80 s and postural stability, in addition to the Expanded Disability Status Scale, Nine Hole Peg Test, Ti
81 ty progression was defined as an increase in Expanded Disability Status Scale of >/= 1.0 compared to
86 hite matter PK11195 BPND correlated with the Expanded Disability Status Scale (P = 0.007; r = 0.672).
88 (p=0.006 and beta-coefficient=-0.67 with the Expanded Disability Status Scale; p=0.003 and beta-coeff
89 an either agent alone in lessening confirmed Expanded Disability Status Scale progression or change i
91 e appropriate Functional Scale scores of the Expanded Disability Status Scale (r = -0.50, P < 0.01).
92 GM, but not WM, fraction correlated with expanded disability status scale (r(s) = -0.48; p < 0.00
93 atients in remission (median age 43.5 years; Expanded Disability Status Scale range 1.5-6.5; 35 relap
95 ickness showed inverse associations with the Expanded Disability Status Scale (rho = -0.295; P = .03
96 oss in spinal cord lesions from 5 paralyzed (Expanded Disability Status Scale score > or =7.5) MS pat
98 k (T25FW) in clinical trial subjects with an Expanded Disability Status Scale score >/=3.5, including
100 5); P < 0.05] and maintenance of ambulation (Expanded Disability Status Scale score < 7) post-transpl
101 es in the 24 months before screening, and an Expanded Disability Status Scale score </= 5.5, were ran
102 ng multiple sclerosis (age 18-65 years, with Expanded Disability Status Scale score </=5) were random
103 ssessed using the ambulation index (AI), the Expanded Disability Status Scale score (EDSS) and the 9-
105 transfer ratio gradient also correlated with Expanded Disability Status Scale score 5 years later (Sp
106 r ratio histogram peak height (P = .02), for Expanded Disability Status Scale score and magnetization
107 fer histogram peak height (P = .02), and for Expanded Disability Status Scale score and percentage of
108 Relapses were confirmed by an increase in Expanded Disability Status Scale score assessed by an in
109 to male ratio, 2.36; mean age, 41 years; and Expanded Disability Status Scale score at the initiation
110 ces in the annualized relapse rate ratio and Expanded Disability Status Scale score before and after
111 redictive value of 78.3% for no progression (Expanded Disability Status Scale score change </=0.5) at
112 most clinical trials rely on progression of Expanded Disability Status Scale score confirmed over 3
113 GM areas had the strongest correlation with Expanded Disability Status Scale score followed by thora
114 ndependent of age, sex, and patient-reported Expanded Disability Status Scale score in a Cox regressi
115 rate was 3.0 (range, 2.3-3.0) and the median Expanded Disability Status Scale score increased from 5.
118 ly powerful for patients with benign MS with Expanded Disability Status Scale score of 2 or lower for
119 Patients had secondary-progressive MS and an Expanded Disability Status Scale score of 3.5 to 6.5 or
120 3 mm on a T2-weighted brain MRI scan, and an Expanded Disability Status Scale score of 5.0 or lower.
122 nsisted of absence of relapses, no sustained Expanded Disability Status Scale score progression, and
125 e range, 0.0-0.8) (P = .008), and the median Expanded Disability Status Scale score significantly dec
126 aquaporin 4-IgG seropositive; and the median Expanded Disability Status Scale score was 4.0 (interqua
127 Annualized relapse rate (ARR), disability (Expanded Disability Status Scale score), change in anti-
130 up to 12 months predicted lower disability (Expanded Disability Status Scale score, -0.17; P = .004)
131 rable in terms of sex, age, body mass index, Expanded Disability Status Scale score, disease duration
139 inal cord area and volume, and scores on the Expanded Disability Status Scale (score range, 0 to 10;
140 ologic disability as assessed by the Kurtzke Expanded Disability Status Scale (score range, 0-10; hig
141 ent vs 0.4 with treatment; P < .001), median Expanded Disability Status Scale scores (2 without treat
142 e had a significantly lower risk of reaching Expanded Disability Status Scale scores 4 (hazard ratio:
143 al: 1.18-1.86) times higher risk of reaching Expanded Disability Status Scale scores 4 and 6 compared
145 from the onset episode, with better recovery Expanded Disability Status Scale scores and a lower risk
147 sensory cortex was associated with increased Expanded Disability Status Scale scores in surface-based
148 he general US population and correlated with Expanded Disability Status Scale scores, sustained disab
150 of multiple sclerosis was determined by the Expanded Disability Status Scale, self-report version.
152 rogression (CDP), a prespecified increase in Expanded Disability Status Scale sustained for 12 weeks.
153 olution (0.57 points annually; P = .04), and Expanded Disability Status Scale sustained progression (
154 (defined as an increase in the score on the Expanded Disability Status Scale that was sustained for
156 6.0 years old, had MS for 6.1 +/- 5.8 years, Expanded Disability Status Scale was 2.2 +/- 0.8, and br
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