Mismatch negativity as a potential neurobiological marker of early-stage Alzheimer disease and vascular dementia

2017 ◽  
Vol 647 ◽  
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Author(s):  
Shixiang Jiang ◽  
Chang Yan ◽  
Zhengxue Qiao ◽  
Haiqian Yao ◽  
Shiquan Jiang ◽  
...  
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Carlo Cervellati ◽  
Cristina Bosi ◽  
Monica Squerzanti ◽  
...  

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pp. 420-420 ◽  
Author(s):  
Katy Malpass

1996 ◽  
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pp. 436-439 ◽  
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A. A. Rizzo ◽  
R. McCleary ◽  
R. Shankle ◽  
M. Dick ◽  
...  

1997 ◽  
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Author(s):  
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A. Pääkkönen ◽  
Jari Karhu ◽  
Juhani Partanen ◽  
Hilkka Soininen ◽  
...  

Neurology ◽  
2010 ◽  
Vol 75 (13) ◽  
pp. 1195-1202 ◽  
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T. Polvikoski ◽  
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A. Solomon ◽  
J. Tuomilehto ◽  
...  

1997 ◽  
pp. 13-17 ◽  
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Helena Chui ◽  
Qian Zhang ◽  
Jeff Victoroff ◽  
Barbara Zaias

2006 ◽  
Vol 81 (10) ◽  
pp. 1350-1358 ◽  
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Martin R. Farlow

2012 ◽  
Vol 18 (2) ◽  
pp. 191-199 ◽  
Author(s):  
Erika J. Laukka ◽  
Stuart W.S. MacDonald ◽  
Laura Fratiglioni ◽  
Lars Bäckman

AbstractWe investigated differences between Alzheimer's disease (AD) and vascular dementia (VaD) from the appearance of the first cognitive symptoms, focusing on both time of onset and rate of accelerated decline for different cognitive functions before dementia diagnosis. Data from a longitudinal population-based study were used, including 914 participants (mean age = 82.0 years, SD = 5.0) tested with a cognitive battery (word recall and recognition, Block Design, category fluency, clock reading) on up to four occasions spanning 10 years. We fit a series of linear mixed effects models with a change point to the cognitive data, contrasting each dementia group to a control group. Significant age-related decline was observed for all five cognitive tasks. Relative to time of diagnosis, the preclinical AD persons deviated from the normal aging curve earlier (up to 9 years) compared to the preclinical VaD persons (up to 6 years). However, once the preclinical VaD persons started to decline, they deteriorated at a faster rate than the preclinical AD persons. The results have important implications for identifying the two dementia disorders at an early stage and for selecting cognitive tasks to evaluate treatment effects for persons at risk of developing AD and VaD. (JINS, 2012, 18, 191–199)


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