2005
DOI: 10.1016/j.neuroscience.2004.09.040
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Hemispheric asymmetry, modular variability and age-related changes in the human entorhinal cortex

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Cited by 54 publications
(52 citation statements)
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“…That fi nding is in accordance with the hemispheric asymmetries recently described in the human entorhinal cortex, a brain region that projects to the hippocampal formation, where leftward size predominance was found 40 . Besides, as the left dentate gyrus contains fewer granule cells than the right one 8 , we may hypothesize that the higher number of dendritic segments that we found in the left side might somewhat compensate for this difference.…”
Section: Discussionsupporting
confidence: 91%
“…That fi nding is in accordance with the hemispheric asymmetries recently described in the human entorhinal cortex, a brain region that projects to the hippocampal formation, where leftward size predominance was found 40 . Besides, as the left dentate gyrus contains fewer granule cells than the right one 8 , we may hypothesize that the higher number of dendritic segments that we found in the left side might somewhat compensate for this difference.…”
Section: Discussionsupporting
confidence: 91%
“…On the contrary, other authors found that left LFC hypometabolism was a feature of stable MCI patients over time [16]. The left LFC contains the language areas and, moreover, is involved in working memory, episodic memory encoding and semantic memory retrieval [17,18]. Conversion to AD mainly entails a worsening episodic and working memory that significantly impairs the everyday functional autonomy, which is consistent with the idea that metabolic failure in these areas is a main PET hallmark of conversion.…”
Section: Fdg-pet Findings In Mild Cognitive Impairment (Mci) and Earlsupporting
confidence: 64%
“…In normal healthy ageing, the global number of microglia [17] or neurons [18] does not decrease significantly. However, a significant decline in neuronal number was detected in several brain regions such as the subiculum and hilus regions of the hippocampus [19] and in the entorhinal cortex [20]. These changes correlate well with the severity of declarative memory decline [21].…”
Section: Functional Histological and Molecular Changes In The Ageingmentioning
confidence: 96%