Please use this identifier to cite or link to this item:
https://ahro.austin.org.au/austinjspui/handle/1/11467
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Carney, Patrick W | - |
dc.contributor.author | Masterton, Richard A J | - |
dc.contributor.author | Flanagan, D | - |
dc.contributor.author | Berkovic, Samuel F | - |
dc.contributor.author | Jackson, Graeme D | - |
dc.date.accessioned | 2015-05-16T01:04:43Z | |
dc.date.available | 2015-05-16T01:04:43Z | |
dc.date.issued | 2012-03-28 | - |
dc.identifier.citation | Neurology 2012; 78(15): 1157-65 | en_US |
dc.identifier.other | PUBMED | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/11467 | en |
dc.description.abstract | Studies of absence seizures (AS) using EEG with fMRI (EEG-fMRI) show a consistent network with prominent thalamic activation and a variety of cortical changes. Despite evidence suggesting a role of frontal cortex in seizure generation, group studies have not detected consistent AS-related changes in this region. We hypothesized that only a subgroup may show frontal cortical activation.We studied 13 subjects with AS during EEG-fMRI to classify the different individual patterns of frontal cortical activation associated with AS.Based upon visual inspection of surface-rendered activation maps we identified 2 subgroups that could be distinguished by the activation in the dorsolateral prefrontal cortex (DLPFC). One group of patients (n = 7) showed a primarily positive signal change (DLPFC-POS), whereas the other group (n = 6) showed a primarily negative signal change (DLFPC-NEG). When the DLPFC-POS group was compared to the DLPFC-NEG group, time-course analysis revealed a larger positive blood oxygenation level-dependent deflection following onset of the AS in cortical and subcortical areas beyond the DLPFC. This suggests a basic biological difference between these groups.These observations suggest that there may be at least 2 mechanisms underpinning AS in individuals with absence epilepsy. This may have phenotypic and genetic implications for understanding epilepsy syndromes. | en_US |
dc.language.iso | en | en |
dc.subject.other | Adolescent | en |
dc.subject.other | Child | en |
dc.subject.other | Child, Preschool | en |
dc.subject.other | Electroencephalography | en |
dc.subject.other | Epilepsy, Absence.pathology.physiopathology | en |
dc.subject.other | Female | en |
dc.subject.other | Frontal Lobe.pathology.physiopathology | en |
dc.subject.other | Humans | en |
dc.subject.other | Magnetic Resonance Imaging | en |
dc.subject.other | Male | en |
dc.subject.other | Prefrontal Cortex.physiopathology | en |
dc.title | The frontal lobe in absence epilepsy: EEG-fMRI findings. | en_US |
dc.type | Journal Article | en_US |
dc.identifier.journaltitle | Neurology | en_US |
dc.identifier.affiliation | Austin Health, Brain Research Institute, Department of Medicine, University of Melbourne, Heidelberg, Victoria, Australia | en_US |
dc.identifier.affiliation | Austin Health | en_US |
dc.identifier.doi | 10.1212/WNL.0b013e31824f801d | en_US |
dc.description.pages | 1157-65 | en |
dc.relation.url | https://pubmed.ncbi.nlm.nih.gov/22459682 | en |
dc.type.content | Text | en_US |
dc.type.austin | Journal Article | en |
local.name.researcher | Berkovic, Samuel F | |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.openairetype | Journal Article | - |
crisitem.author.dept | Neurology | - |
crisitem.author.dept | Epilepsy Research Centre | - |
crisitem.author.dept | Neurology | - |
crisitem.author.dept | Neurology | - |
crisitem.author.dept | The Florey Institute of Neuroscience and Mental Health | - |
Appears in Collections: | Journal articles |
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