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dc.contributor.authorFernandez, Francescaen_US
dc.contributor.authorColson, Natalieen_US
dc.contributor.authorGriffiths, Lynen_US
dc.contributor.editorLaura Dormeren_US
dc.date.accessioned2017-04-24T11:20:35Z
dc.date.available2017-04-24T11:20:35Z
dc.date.issued2007en_US
dc.date.modified2009-01-23T05:37:49Z
dc.identifier.issn14622416en_US
dc.identifier.doi10.2217/14622416.8.6.609en_AU
dc.identifier.urihttp://hdl.handle.net/10072/17846
dc.description.abstractMigraine is a paroxysmal neurological disorder affecting up to 6% of males and 18% of females in the general population, and has been demonstrated to have a strong, but complex, genetic component. Genetic investigation of migraine provides hope that new targets for medications and individual specific therapy will be developed. The identification of polymorphisms or genetic biomarkers for disease susceptibility and treatment should aid in providing a better understanding of migraine pathology and, consequently, more appropriate and efficient treatment for migraineurs. In this review, we will discuss results investigating genetic biomarkers for migraine and their potential role in future therapy planning.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherFuture Medicine Ltden_US
dc.publisher.placeLondon UKen_US
dc.publisher.urihttp://www.futuremedicine.com/loi/pgsen_AU
dc.relation.ispartofstudentpublicationNen_AU
dc.relation.ispartofpagefrom609en_US
dc.relation.ispartofpageto622en_US
dc.relation.ispartofissue6en_US
dc.relation.ispartofjournalPharmacogenomicsen_US
dc.relation.ispartofvolume8en_US
dc.rights.retentionYen_AU
dc.subject.fieldofresearchcode320799en_US
dc.titlePharmacogenetics of Migraine: genetic variants and their potential role in migraine therapyen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.facultyGriffith Health, School of Medical Scienceen_US
gro.date.issued2007
gro.hasfulltextNo Full Text


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