Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/21406
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dc.contributor.advisorRIGO, Jean-Michel-
dc.contributor.authorSWIJSEN, Ann-
dc.date.accessioned2016-06-02T18:46:52Z-
dc.date.available2016-06-02T18:46:52Z-
dc.date.issued2011-
dc.identifier.urihttp://hdl.handle.net/1942/21406-
dc.description.abstractIn this thesis, we aimed at elucidating some mechanisms by which early-life FS may lead to enhanced hippocampal excitability. We focused on the DG structure and investigated if FS-induced expressional and functional alterations of ligandgated ion channels (LGICs) in the DG may contribute to a disturbed DG ‘gate’ function. To this end, we used an appropriate-aged animal model in which FS are evoked in 10-day old rat pups by exposing them to heated air. In this model, FS are associated with long-term hippocampal hyperexcitability resulting in a decreased seizure threshold. 35% of rats with early-life FS develop TLE in adulthood, while 88% show interictal epileptoform EEG abnormalities. ...-
dc.language.isoen-
dc.titleThe role of ligand-gated ion channels after early-life febrile seizures-
dc.typeTheses and Dissertations-
local.format.pages136-
local.bibliographicCitation.jcatT1-
local.type.refereedNon-Refereed-
local.type.specifiedPhd thesis-
item.accessRightsOpen Access-
item.fullcitationSWIJSEN, Ann (2011) The role of ligand-gated ion channels after early-life febrile seizures.-
item.fulltextWith Fulltext-
item.contributorSWIJSEN, Ann-
Appears in Collections:PhD theses
Research publications
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