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1 f dementia severity measured by the Clinical Dementia Rating Scale.
2 up assessments were obtained with the Mattis Dementia Rating Scale.
3 for dementia severity by using the Clinical Dementia Rating Scale.
4 alidated proxy measure, the Modified Blessed Dementia Rating Scale.
5 sychopathology rating scales, and the Mattis Dementia Rating Scale.
6 Mental State Examination (MMSE) and Clinical Dementia Rating scale.
7 ases was also done by employing the Clinical Dementia Rating Scale.
8 y Mini-Mental State Examination and Clinical Dementia Rating scales.
9 ore, 1-step worsening on the global Clinical Dementia Rating scale, 15-point decline on the ADCS acti
10 gnitive status was evaluated with the Mattis Dementia Rating Scale-2 (DRS) at baseline and on annual
11 -Mental State Examination (MMSE), the Mattis Dementia Rating Scale-2 (DRS-2), and the Clinical Dement
13 Rating Scale-2, and new robust and expanded Dementia Rating Scale-2 norms were applied to cognitivel
14 onance imaging brain scans and completed the Dementia Rating Scale-2, and new robust and expanded Dem
16 and a positive association with the Clinical Dementia Rating Scale (a global functional assessment).
17 e was a negative association with the Mattis Dementia Rating Scale (a global measure of cognition) an
18 eline and every 15 months using the Clinical Dementia Rating scale, a neurological evaluation, and ne
19 nalysis of covariance adjusting for baseline Dementia Rating Scale, age, gender, magnetic resonance f
20 annually for up to 4 years with the Clinical Dementia Rating scale and a battery of neuropsychologica
21 rogate interviews using the Modified Blessed Dementia Rating Scale and a review of medical records.
23 rders were administered the UPSA, the Mattis Dementia Rating Scale, and standardized measures of psyc
25 tiation/perseveration subscore of the Mattis Dementia Rating Scale, and the latency of the P300 audit
29 uded 468 healthy older individuals (Clinical Dementia Rating scale [CDR] global scores of 0, above cu
30 ysfunction and memory were assessed with the Dementia Rating Scale, disability and social support wer
31 rment at baseline, performance on the Mattis Dementia Rating Scale domains of conceptualization and i
32 nically healthy older participants (Clinical Dementia Rating Scale global scores of 0) participating
34 tionship of age to performance on the Mattis Dementia Rating Scale in 116 outpatients with schizophre
36 with total and subscale scores on the Mattis Dementia Rating Scale, level of independence in the comm
40 increased serum ACT correlated with Clinical Dementia Rating Scale (p = 0.0041) or Mattis Dementia Ra
41 provement, stable or reliable decline) using Dementia Rating Scale reliable change indices determined
42 rebrospinal fluid correlated with the Mattis Dementia Rating Scale score (Pearson r = 0.50; P = .03)
43 nation score of 17 or less, baseline Blessed Dementia Rating Scale score of 5.0 or greater, presence
44 menting disorders, the mean (+/-SD) Clinical Dementia Rating Scale score was 2.21 (+/-1.14), with 43
45 ients of differing dementia severity (Mattis Dementia Rating Scale score, 23-128) and in 14 age-match
46 Mini-Mental State Examination score, Blessed Dementia Rating Scale score, duration since reported ons
48 waves were negatively correlated with Mattis Dementia Rating Scale scores for initiation/perseveratio
52 cognitive profiles of the two groups on the Dementia Rating Scale subscales were identical, with the
53 ion level was associated with lower Clinical Dementia Rating Scale sum of boxes (beta = -0.19; P < .0
54 plaques were associated with higher Clinical Dementia Rating Scale sum of boxes (beta = 1.64; P < .00
56 ement in slope in rate of change of Clinical Dementia Rating Scale sum of boxes has 89% power when al
57 standard clinical instruments: the Clinical Dementia Rating Scale sum of boxes, a verbal memory test
58 tein Mini-Mental State Examination, Clinical Dementia Rating Scale Sum of Boxes, Logical Memory Immed
59 ange, 0-30, with 30 being best) and Clinical Dementia Rating scale sum-of-boxes scale (range, 0-18, w
61 ndary outcome measures included the Clinical Dementia Rating scale sum-of-boxes, the Neuropsychiatric
64 tiation-perseveration subscale of the Mattis Dementia Rating Scale, Trail Making tests A and B, and D
65 Longitudinally, decline in the Clinician's Dementia Rating scale was correlated with decline in mag
66 ni-Mental State Examination and the Clinical Dementia Rating scale, was detected 5 years before expec
68 ferences, with the exception of the Clinical Dementia Rating Scale, which suggested worsening among p
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