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https://ahro.austin.org.au/austinjspui/handle/1/11453
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Carranza Rojo, Daniel | en |
dc.contributor.author | Harvey, A Simon | en |
dc.contributor.author | Iona, Xenia | en |
dc.contributor.author | Dibbens, Leanne M | en |
dc.contributor.author | Damiano, John Anthony | en |
dc.contributor.author | Arsov, Todor | en |
dc.contributor.author | Gill, Deepak S | en |
dc.contributor.author | Freeman, Jeremy L | en |
dc.contributor.author | Leventer, Richard J | en |
dc.contributor.author | Vincent, Angela | en |
dc.contributor.author | Berkovic, Samuel F | en |
dc.contributor.author | McMahon, Jacinta M | en |
dc.contributor.author | Scheffer, Ingrid E | en |
dc.date.accessioned | 2015-05-16T01:03:52Z | |
dc.date.available | 2015-05-16T01:03:52Z | |
dc.date.issued | 2012-03-03 | en |
dc.identifier.citation | Epilepsy Research 2012; 100(1-2): 194-8 | en |
dc.identifier.govdoc | 22386634 | en |
dc.identifier.other | PUBMED | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/11453 | en |
dc.description.abstract | Two distinctive epileptic encephalopathies, febrile infection-related epilepsy syndrome (FIRES) and Dravet syndrome (DS), present with febrile status epilepticus in a normal child followed by refractory focal seizures and cognitive decline although there are differentiating features. Abnormalities of the sodium channel gene SCN1A are found in 75% of DS patients. We found no SCN1A mutations or copy number variants in 10 patients with FIRES. Other genetic etiologies deserve consideration. | en |
dc.language.iso | en | en |
dc.subject.other | Adolescent | en |
dc.subject.other | Adult | en |
dc.subject.other | Child, Preschool | en |
dc.subject.other | Diagnosis, Differential | en |
dc.subject.other | Epilepsies, Myoclonic.genetics | en |
dc.subject.other | Humans | en |
dc.subject.other | Mutation.genetics | en |
dc.subject.other | NAV1.1 Voltage-Gated Sodium Channel.genetics | en |
dc.subject.other | Seizures, Febrile.diagnosis.genetics | en |
dc.subject.other | Young Adult | en |
dc.title | Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations. | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | Epilepsy research | en |
dc.identifier.affiliation | Epilepsy Research Centre, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia | en |
dc.identifier.doi | 10.1016/j.eplepsyres.2012.02.007 | en |
dc.description.pages | 194-8 | en |
dc.relation.url | https://pubmed.ncbi.nlm.nih.gov/22386634 | en |
dc.type.austin | Journal Article | en |
local.name.researcher | Berkovic, Samuel F | |
item.languageiso639-1 | en | - |
item.openairetype | Journal Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Epilepsy Research Centre | - |
crisitem.author.dept | Neurology | - |
crisitem.author.dept | Epilepsy Research Centre | - |
Appears in Collections: | Journal articles |
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