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Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11318
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dc.contributor.authorScheffer, Ingrid Een
dc.date.accessioned2015-05-16T00:54:27Z
dc.date.available2015-05-16T00:54:27Z
dc.date.issued2011-07-01en
dc.identifier.citationEpilepsy Currents / American Epilepsy Society; 11(4): 107-11en
dc.identifier.govdoc21836823en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11318en
dc.description.abstractWith the burgeoning array of molecular tests available in the epilepsies, the clinician needs to know which tests to order for each patient. Epileptic encephalopathies are the most important clinical group for genetic testing with an increasing number of distinctive epilepsy syndromes being recognized. Identification of the causative mutation affects treatment as well as prognostic and genetic counseling.en
dc.language.isoenen
dc.titleGenetic testing in epilepsy: what should you be doing?en
dc.typeJournal Articleen
dc.identifier.journaltitleEpilepsy currents / American Epilepsy Societyen
dc.identifier.affiliationProfessor of Paediatric Neurology, Departments of Medicine and Paediatrics, The University of Melbourne, Austin and Royal Children's Hospital, Senior Principal Research Fellow, Florey Neuroscience Institutes, and Director of Paediatrics, Austin Health, Melbourne, Australiaen
dc.identifier.doi10.5698/1535-7511-11.4.107en
dc.description.pages107-11en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/21836823en
dc.type.austinJournal Articleen
local.name.researcherScheffer, Ingrid E
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptEpilepsy Research Centre-
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