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1 sures (pain severity, upper limb disability, disease duration).
2 n serum correlated with disease severity and disease duration.
3 Panuveitis was associated with longer disease duration.
4 her pathologic variables are associated with disease duration.
5 in comparison to controls and increased with disease duration.
6 experience smaller disease burden and longer disease duration.
7 efficiency was significantly correlated with disease duration.
8 t disease severity and is independent of the disease duration.
9 Disease severity increased with disease duration.
10 tion of regional and total brain scores with disease duration.
11 ymptoms and signs, rates of progression, and disease duration.
12 patients and weaker in patients with longer disease duration.
13 easurements and pulmonary function tests and disease duration.
14 f early active plaques rapidly declined with disease duration.
15 ecline of clinical outcome measures based on disease duration.
16 effect of TREM2 genotype on age at onset and disease duration.
17 s of retinal atrophy, decline in vision, and disease duration.
18 entral macular thickness, visual acuity, and disease duration.
19 nent cerebellar signs, which were related to disease duration.
20 ly in the inner layers of patients with long disease duration.
21 ndent from age, sex, biological markers, and disease duration.
22 ity as measured by several rating scales and disease duration.
23 cted in Parkinson disease patients with long disease duration.
24 area, number of SC T2 lesions, age, sex, and disease duration.
25 fy biomarker panels that could predict total disease duration.
26 -nitrotyrosine, both of which increased with disease duration.
27 out of STN DBS effects varies with Parkinson disease duration.
28 s in the NAWM of MS patients with increasing disease duration.
29 parkin-mutation carriers (<3%), despite long disease duration.
30 f controls as well as in patients with short disease duration.
31 nt, and increased survival without modifying disease duration.
32 idual VRF on DF and JCL, considering age and disease duration.
33 xhibited correlations with anxiety level and disease duration.
34 ration, age at Parkinson's disease onset and disease duration.
35 ODI and ISO correlated with disease duration.
36 tive impairment, after adjusting for age and disease duration.
37 adjusting atopy status, smoking history, and disease duration.
38 aggressive disease course, rather than long disease duration.
39 memory and psychomotor speed correlated with disease duration.
40 , Expanded Disability Status Scale score and disease duration.
41 significantly associated with differences in disease duration.
42 complex profiles were associated with longer disease duration.
43 al group and patients with bvFTD had similar disease durations.
44 may not apply to populations with different disease durations.
45 ion of patients with low EDSS scores at long disease durations.
46 ancreata across a wide range of ages and T1D disease durations.
47 patients with relapsing-remitting MS (median disease duration, 0.8 year) were analyzed by using the s
48 signed (mean age, 62 years [SD, 9]; 68% men; disease duration, 0.9 year [SD, 0.7]; mean UPDRS part I
49 s disease (11 females, age 57 +/- 9.1 years, disease duration 13.3 +/- 6.3 years) who received bilate
50 ng-remitting multiple sclerosis (>/= 4 years disease duration), 13 subjects with secondary progressiv
51 d 264 MS patients (mean age 46.9+/-10 years, disease duration 14.6+/-10 years; 67.8% relapsing-remitt
53 omen; monthly attack frequency: 3.2 +/- 2.5; disease duration: 14 +/- 8.4 years) and 115 matched heal
55 ndrome/early multiple sclerosis (</= 3 years disease duration), 18 subjects with relapsing-remitting
56 29 subjects with mild-to-moderate PD (median disease duration = 2.3+/-1.9 years) and 18 healthy match
57 Patients with somatic mutations had a longer disease duration (37 vs 8 months, P < .04), and shorter
58 ve patients with probable AD and matched for disease duration (45 German-Italian bilingual speakers a
60 62 +/- 7 years; education = 16 +/- 3 years; disease duration = 5.8 +/- 3.9 years) and 27 controls (a
61 patients (13 males and 18 females; mean [SD] disease duration, 5.9 [3.6] years), bright LT resulted i
62 female; mean age at death 64.7 years; median disease duration 6.5 years, range 2.2 to 15.6 years).
63 men and 160 men (mean age = 43 years, median disease duration = 6 years, median EDSS = 1.5 [range = 0
64 (23 men and 7 women; mean age, 66 +/- 6.2 y; disease duration, 6.4 +/- 4.0 y; Hoehn and Yahr stage, 2
65 of 79 patients with newly diagnosed PD (mean disease duration 8 months) and 20 unrelated controls.
66 s disease (mean age 63.8 years +/- 6.8; mean disease duration 9.4 years +/- 2.5) both OFF and ON levo
67 and 41% of that with SARA were explained by disease duration, age at onset and the shorter abnormal
68 e compulsive behaviours matched by age, sex, disease duration, age at Parkinson's disease onset and d
70 sion analysis, choroidal thickness, age, and disease duration (all P < 0.01) all were significant pre
71 A correlation between radial diffusivity and disease duration along the corticospinal tracts (r = 0.8
73 r monogenic dystonias, adjusting for age and disease duration and (iii) weighted linear regression an
74 tients needed walking aids after 10 years of disease duration and a quarter were wheelchair dependent
75 mutation except for an indication of longer disease duration and age in patients with highest mutati
80 ortem neuroimaging, directly correlated with disease duration and inversely correlated with brain wei
85 ns, which showed a negative correlation with disease duration and overlapped with striatal regions sh
86 ayer thickness was inversely correlated with disease duration and Parkinson disease severity, and was
94 significant correlation was observed between disease duration and the Expanded Disability Status Scal
97 th diabetes mellitus (especially with longer disease duration) and hyperlipidemia or obesity were ass
98 repeat expansion by analyzing age at onset, disease duration, and age at death in successive generat
99 The generational effect on age at onset, disease duration, and age at death was estimated using a
102 Data concerning demographics, age at onset, disease duration, and clinical and pathological features
104 t Thal amyloid phase predicted age at onset, disease duration, and final Mini-Mental State Examinatio
105 maternal education, seizure disorder, kidney disease duration, and genetically defined ancestry.
106 Randomization was balanced for age, sex, disease duration, and glutamic acid decarboxylase autoan
107 ith pain had an earlier age of onset, longer disease duration, and higher depression and motor severi
108 oss used a linear mixed model with sex, age, disease duration, and HLA-DRB1*15:01 as covariates.
109 to evaluate the influence of baseline BCVA, disease duration, and ischemia on BCVA outcomes at month
113 on functional class, 6-minute walk distance, disease duration, and red cell distribution width also p
117 phy was correlated with clinical disability, disease duration, and, to a lesser extent, conventional
118 lzheimer's disease with distinctly different disease durations, and correlated the data with APOE gen
119 dex, Expanded Disability Status Scale score, disease duration, annual relapse rate, and treatment sta
121 , 0.37; P=0.004), and infants with a shorter disease duration at screening were more likely than thos
124 analysis adjusted by sex, age at onset, and disease duration attributed to GBA carriers a greater ri
125 bjects (n = 12) with approximately 30 years, disease duration before and 6 months after intrahepatic
127 fferences in age at onset, age at death, and disease duration between genetic groups and individual m
130 version recovery lesion loads, age, sex, and disease duration), cervical cord GM areas had the strong
131 31.4 +/- 9.0; RRMS: 33.0 +/- 8.7 years; mean disease duration: CIS: 7.2 +/- 15 months; RRMS: 8.0 +/-
133 ya disease and estimate its burden regarding disease duration, clinical presentation, and impact on q
134 1, 2011, and Nov 3, 2016, 244 patients (mean disease duration: clinical management group, 0.9 years [
135 independent cohorts (72 patients with short disease duration [cohort 1] and 240 patients with longer
136 tion [cohort 1] and 240 patients with longer disease duration [cohort 2]) treated at a single German
137 neocortical) LBD was associated with shorter disease duration compared with transitional LBD (beta, -
138 Diffuse LBD was associated with shorter disease duration compared with transitional LBD, and thi
139 ANG-ALS, we assembled all clinical onset and disease duration data and determined if these were corre
141 ds models that included OCT metrics and age, disease duration, disability, presence of previous unila
142 There was no relationship of PHOMS with age, disease duration, disease course, disability, or disease
144 logistic regression, adjusting for sex, age, disease duration, duration of follow-up, years of educat
147 d to disease duration: patients with shorter disease duration experienced slower washout, while patie
148 cinosis is positively associated with longer disease duration, fingertip ulcers, and NXP-2 autoantibo
150 attack (54 months) was similar to the median disease duration for AQP4-IgG-positive patients with rLE
151 a on age at symptom onset, age at death, and disease duration for patients with pathogenic mutations
155 vailable on sex, age at motor symptom onset, disease duration (from motor symptom onset to death or t
156 pathic cardiomyopathy (0.4 [0.2-1]), cardiac disease duration greater than 2 years pre-extracorporeal
157 patients with MS of long-standing duration (disease duration >/= 10 years) and in 60 healthy control
158 igible patients (ie, those aged 18-75 years, disease duration >/=3 years, Toronto Western Spasmodic T
159 neurysm was 4.2-fold higher in patients with disease duration >5 years (p = 0.042, OR = 4.237, 95% CI
163 ly those with a short diagnostic latency and disease duration, had higher plasma NfH levels at an ear
164 oratory data of diabetic patients, including disease duration, haemoglobin A1c (HbA1c) levels and uri
165 hazards analyses adjusting for age, sex, and disease duration (hazard ratio [HR] 2.27 [95% CI 1.04-5.
166 hey did differ significantly with respect to disease duration; hemoglobin level; frequency of thrombo
168 t; (ii) a correlation between IL6 levels and disease duration in carriers of PRKN/PINK1 mutations, wh
171 y of age at symptom onset, age at death, and disease duration in individuals with mutations in GRN, M
175 IGF1 levels significantly decreased with disease duration, in parallel with declining beta-cell f
178 Models were adjusted for age, education, disease duration, language, and levodopa equivalent dail
179 phic data, smoking status, age at diagnosis, disease duration, location, and behaviour, previous medi
180 six early stage multiple sclerosis subjects (disease duration </=5 years) and 24 age-matched healthy
182 yes or no), weight (<70 kg or >/=70 kg), and disease duration (</=2 years or >2 years) after 8 weeks
185 chronic disease phase and 65 age-, sex-, and disease duration-matched multiple sclerosis patients.
186 ment for levodopa equivalent dose, sex, age, disease duration, MDS-UPDRS III score at the first asses
188 medications at baseline had longer diabetes disease duration (mean, 17.4 and 20.9 years, respectivel
189 ed as semantic dementia, and they had longer disease duration (mean: 15.3 years) compared with the ot
190 ith vs those without calcinosis had a longer disease duration (median, 6.9 years; range, 2.4-18.1; vs
191 .0 years [IQR, 26.3-38.3 years]), with short disease durations (median, 1.0 months [IQR, 1.0-2.0 mont
192 0 years]) consisting of patients with longer disease durations (median, 36.0 months [IQR, 21.0-60.0 m
194 5 +/- 7.4 years old; 6.0 +/- 4.2 years motor disease duration; modified Hoehn and Yahr mean stage 2.4
195 e, younger, younger at PD onset, have longer disease duration, more severe non-motor symptoms (includ
197 sociated with the primary outcome were short disease duration (odds ratio [OR] 0.64, 95% CI 0.41-0.99
198 ubjects and 30 PD patients at early stage of disease (duration of disease </= 5 y) with mild and unil
200 <1 year (group A [n = 80]) and those with a disease duration of >5 years (group B [n = 120]) were in
201 Somatic mutations in AA patients with a disease duration of >6 months were associated with a 40%
202 s (n = 200) with noninfectious uveitis and a disease duration of <1 year (group A [n = 80]) and those
204 et of 15.3 years (range, 3-28 years), a mean disease duration of 12.1 years, and a mean age at baseli
205 Additional eligibility criteria included disease duration of 2-10 years and objective evidence of
206 hort of 61 patients with T1D with an average disease duration of 21 years with 54 well-matched contro
208 ability to walk independently after a median disease duration of 23 years and became wheelchair depen
212 an age, 76.7 years; 93.5% men) with a median disease duration of 55.6 months and mild to moderate hea
215 ernational panel criteria for diagnosis with disease duration of less than 15 years were eligible.
216 ized nonthymomatous myasthenia gravis with a disease duration of less than 5 years were included if t
217 vere underweight, severe acute malnutrition, disease duration of more than 21 days, and referral from
218 and between Parkinson disease patients with disease durations of less than or at least 10 years.
220 mixed-effects models adjusting for age, sex, disease duration, optic neuritis and genetic ancestry an
223 led to show a benefit in patients with short disease duration or an increased level of C-reactive pro
225 (%CCR9) in SPMS did not correlate with age, disease duration or expanded disability status scale sco
226 f glucocorticoids (weak evidence) but not to disease duration or severity/activity, gender, age, or A
228 g the SP phase increased proportionally with disease duration (OR=1.07 for each additional year; p<0.
229 etween GABA responses, demographic features, disease duration, or disease severity in the whole popul
231 exponentially at a rate of 7.3% per year of disease duration (P < .001, 95% CI 5.4-9.1), and ellipso
232 exponentially at a rate of 8.1% per year of disease duration (P < .001, 95% confidence interval [CI]
233 halamus and brainstem correlated with longer disease duration (P < 0.05) and higher disease burden sc
237 nzymatic activity was associated with longer disease duration (P = 0.002) in adjusted models, suggest
238 n severity was significantly associated with disease duration (P = 0.02), and COMT rs6267 T allele (P
240 5 <5 x 109/L) and was associated with longer disease duration (P = 7 x 10-6), lower nadir platelet co
242 ohort, eotaxin-1 (CCL11) was associated with disease duration particularly in patients who had second
244 , and this variation was strongly related to disease duration: patients with shorter disease duration
246 founding factors of sexual dysfunction: age; disease duration; physical disability; depression; bladd
248 regression adjusted for age, calendar year, disease duration, propensity scores, and use of other IB
249 l variability, which was not associated with disease duration (R (2) = 0.1, p > 0.2), did correlate w
250 0.6) at follow-up (P = .001) correlated with disease duration (r = 0.47, P = .003 at baseline and r =
251 e choriocapillaris and the Sattler layer and disease duration (R2 = 0.98 and R2 = 0.99, respectively;
252 e hippocampus and parahippocampus revealed a disease duration-related increase in neuronal cytoplasmi
253 ree of atrophy (rho = -0.585, p = 0.011) and disease duration (rho = 0.632, p = 0.005) in the anterom
254 found between the (11)C-donepezil signal and disease duration, severity of constipation, gastric empt
257 remaining insulin-containing islets and long disease duration show elevated levels of CD8 T cells in
258 multivariate model adjusted for age, gender, disease duration, smoking status, vitamin D levels, body
259 r performance than did noncarriers with long disease duration, suggesting slower disease progression.
260 dementia with Lewy bodies (DLB) have shorter disease duration than patients with Alzheimer disease de
261 the lower extremities, which correlates with disease duration (thigh fat fraction R(2) = 0.35, p = 0.
263 PD-ICB were matched for age, gender and disease duration to 42 patients with PD without ICB over
266 The objective of this study was to document disease duration, treatment history, and disease activit
267 anded Disability Status Scale (EDSS) scores, disease duration, treatments, prior optic neuritis episo
269 ificantly exponential correlations to stage; disease duration; Unified Parkinson Disease Rating Scale
270 body levels and influenza viral shedding and disease duration using accelerated failure time models.
279 ) age was 39.5 (11.2) years and preoperative disease duration was 97.9 (85.8) months; 83 patients (91
280 s. 270.05+/-24.6 mum; P = 0.04), and greater disease duration was associated with decreases in retina
284 een onset of motor and dementia symptoms and disease duration was shorter (p<0.0001 for all compariso
288 Earlier age of seizure onset and longer disease duration were associated with a greater extent o
290 On multivariate analysis, HGD, DALM, and disease duration were independent risk factors for posto
291 ilability at rest positively correlated with disease duration were lateral and non-overlapping with s
292 with CMTNSv2, SF-36v2-physical component and disease duration were MRI determined calf intramuscular
293 Lithium medication, later onset and short disease duration were related to higher FA along multipl
297 ctions were greater in patients with shorter disease duration, which suggests a potential benefit of
298 ma tACS on single-pulse MEPs correlated with disease duration, while changes in SICI correlated with
299 nresponders spent 54% and 97% of their total disease duration with active EoE (P < .001) and 23% and
300 gan donors with type 1 diabetes with a short disease duration with high-risk HLA genes using a direct