scholarly journals Quantification of myelin loss in frontal lobe white matter in vascular dementia, Alzheimer’s disease, and dementia with Lewy bodies

2010 ◽  
Vol 119 (5) ◽  
pp. 579-589 ◽  
Author(s):  
Masafumi Ihara ◽  
Tuomo M. Polvikoski ◽  
Ros Hall ◽  
Janet Y. Slade ◽  
Robert H. Perry ◽  
...  
NeuroImage ◽  
2007 ◽  
Vol 36 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Michael J. Firbank ◽  
Andrew M. Blamire ◽  
Mani S. Krishnan ◽  
Andrew Teodorczuk ◽  
Philip English ◽  
...  

Neurology ◽  
2000 ◽  
Vol 54 (8) ◽  
pp. 1616-1625 ◽  
Author(s):  
M. P. Walker ◽  
G. A. Ayre ◽  
J. L. Cummings ◽  
K. Wesnes ◽  
I. G. McKeith ◽  
...  

2011 ◽  
Vol 45 (8) ◽  
pp. 1095-1100 ◽  
Author(s):  
Kuniaki Kiuchi ◽  
Masayuki Morikawa ◽  
Toshiaki Taoka ◽  
Soichiro Kitamura ◽  
Tomohisa Nagashima ◽  
...  

1999 ◽  
Vol 174 (1) ◽  
pp. 45-50 ◽  
Author(s):  
Clive Holmes ◽  
Nigel Cairns ◽  
Peter L. Lantos ◽  
Anthony Mann

BackgroundFollowing the success of the NINCDS–ADRDA criteria for Alzheimer's disease, groups interested in vascular dementia and dementia with Lewy bodies have now adopted similar criteria.AimsTo assess whether the validity of these criteria are influenced by the prevalence of mixed pathologies or by the prevalence rate.MethodA community based postmortem study.ResultsMixed pathologies were common (33.8%). The high specificities obtained for the CDLB and NINDS–AIREN criteria (1.00 and 0.95, respectively) were associated with low sensitivities (0.22 and 0.43, respectively). Low prevalence and the presence of mixed pathologies had a deleterious effect on positive predictive values.ConclusionsCurrent clinical diagnostic criteria are good at detecting pathology per se but not at detecting pure pathology. A large proportion of subjects from the general population fulfilling probable CDLB, probable NINCDS–ADRDA or probable NINDS–AIREN will have mixed pathologies.


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