2011
DOI: 10.1016/j.yebeh.2011.04.005
|View full text |Cite
|
Sign up to set email alerts
|

Geriatric epilepsy: Research and clinical directions for the future

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

4
14
0
1

Year Published

2012
2012
2020
2020

Publication Types

Select...
7
1

Relationship

0
8

Authors

Journals

citations
Cited by 17 publications
(19 citation statements)
references
References 111 publications
4
14
0
1
Order By: Relevance
“…Similar findings had been published previously [16,17,19]. Our findings are consistent with already reported verbal memory deterioration following dominant temporal lobe surgery [7,18,19,20].…”
Section: Discussionsupporting
confidence: 93%
See 1 more Smart Citation
“…Similar findings had been published previously [16,17,19]. Our findings are consistent with already reported verbal memory deterioration following dominant temporal lobe surgery [7,18,19,20].…”
Section: Discussionsupporting
confidence: 93%
“…It is estimated that the number of people aged 65 and older will double between 2010 and 2050. A fourfold increase is expected among persons over the age of 85 [18].…”
Section: Discussionmentioning
confidence: 99%
“…In the present study, in agreement with the literature, practically two thirds of the cases were diagnosed as symptomatic epilepsy, and the etiology identified with greater frequency was cerebrovascular disease in approximately 55% of the cases and in a similar proportion for both age groups 2,6,8,9,15,24 .…”
Section: Epileptic Syndromes Symptomatic Epilepsysupporting
confidence: 92%
“…The following etiologies were also found, equally in agreement with the literature: traumatic brain injury, intracranial arteriovenous malformation and degenerative disease 6,8,24 . The etiology was neurocysticercosis in two cases, with viable cysts visible in the neuroimaging exam.…”
Section: Epileptic Syndromes Symptomatic Epilepsysupporting
confidence: 89%
“…However, the neocortical layer of most severe neuronal loss and in adult tauopathies is layer 2 [34] and the phosphorylated tau expression in all of our infantile cases of HME was also in the superficial laminae of the cortex, showing a similar gradient within the cortex. Tau over-expression is not specific to HME in paediatric brain tissue, but the only other malformations which share this feature, to our knowledge, are tuberous sclerosis and focal cortical dysplasia type IIb, with balloon cells and dysplastic neurons, which also share the same property of mTOR activation [40,49]. Tau over-expression is also reported many years following traumatic contusions of the brain [22].…”
Section: Discussionmentioning
confidence: 76%