Show simple item record

Effects of Vagus Nerve Stimulation on Progressive Myoclonus Epilepsy of Unverricht-Lundborg Type

dc.contributor.authorSmith, Brien J.en_US
dc.contributor.authorShatz, Rhonnaen_US
dc.contributor.authorElisevich, Kosten_US
dc.contributor.authorBespalova, Irina N.en_US
dc.contributor.authorBurmeister, Margit L.en_US
dc.date.accessioned2010-04-01T15:05:08Z
dc.date.available2010-04-01T15:05:08Z
dc.date.issued2000-08en_US
dc.identifier.citationSmith, Brien; Shatz, Rhonna; Elisevich, Kost; Bespalova, Irina N.; Burmeister, Margit (2000). "Effects of Vagus Nerve Stimulation on Progressive Myoclonus Epilepsy of Unverricht-Lundborg Type." Epilepsia 41(8): 1046-1048. <http://hdl.handle.net/2027.42/65549>en_US
dc.identifier.issn0013-9580en_US
dc.identifier.issn1528-1167en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/65549
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=10961635&dopt=citationen_US
dc.description.abstractPurpose : A 34-year-old woman with progressive myoclonus epilepsy of Unverricht-Lundborg type was considered for vagus nerve stimulation (VNS) therapy. Methods : After demonstration of intractability to multiple antiepileptic regimens and progressive deterioration in cerebellar function, the patient was implanted with a vagus nerve stimulator and followed for 1 year. Neurological status, seizure frequency, and parameter changes were analyzed. Results : VNS therapy resulted in reduction of seizures (more than 90%) and a significant improvement in cerebellar function demonstrated on neurological examination. The patient reported improved quality of life based in part on her ability to perform activities of daily living. Conclusions : VNS therapy may be considered a treatment option for progressive myoclonus epilepsy. The effects of VNS on seizure control and cerebellar dysfunction may provide clues to the underlying mechanism(s) of action.en_US
dc.format.extent323608 bytes
dc.format.extent3110 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.rights2000 International League Against Epilepsyen_US
dc.subject.otherVagus Nerveen_US
dc.subject.otherProgressive Myoclonus Epilepsyen_US
dc.subject.otherElectrical Stimulationen_US
dc.subject.otherEpilepsyen_US
dc.subject.otherSeizureen_US
dc.titleEffects of Vagus Nerve Stimulation on Progressive Myoclonus Epilepsy of Unverricht-Lundborg Typeen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMedicine (General)en_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Neurology, Henry Ford Health System, Detroit, Michigan, U.S.A.en_US
dc.contributor.affiliationum* Department of Neurosurgery, Henry Ford Health System, Detroit, Michigan, U.S.A.en_US
dc.contributor.affiliationum† Mental Health Research Institute, University of Michigan, Ann Arbor, Michigan, U.S.A.en_US
dc.contributor.affiliationum† Department of Psychiatry, University of Michigan, Ann Arbor, Michigan, U.S.A.en_US
dc.identifier.pmid10961635en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/65549/1/j.1528-1157.2000.tb00293.x.pdf
dc.identifier.doi10.1111/j.1528-1157.2000.tb00293.xen_US
dc.identifier.sourceEpilepsiaen_US
dc.identifier.citedreference1. Marseille Consensus Group. Classification of progressive myoclonus epilepsies and related disorders. Consensus statement, American Neurological Association. Ann Neurol 1990 ; 28 : 113 – 6.en_US
dc.identifier.citedreferenceLehesjoki AE, Koskiniemi M, Sistonen P, et al. Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22. Genetics 1991 ; 88 : 3696 – 9.en_US
dc.identifier.citedreferencePennacchio LA, Lehesjoki AE, Stone NE, et al. Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1). Science 1996 ; 271 : 1731 – 4.en_US
dc.identifier.citedreferenceIivanainen M, Himberg JJ. Valproate and clonazepam in the treatment of severe progressive myoclonus epilepsy. Arch Neurol 1982 ; 39 : 236 – 8.en_US
dc.identifier.citedreferenceKoskiniemi M, Van Vleymen B, Hakamies L, Lamusuo S, Taalas J. Piracetam relieves symptoms in progressive myoclonus epilepsy: a multicentre, randomised, double blind, crossover study comparing the efficacy and safety of three dosages of oral piracetam with placebo. J Neurol Neurosurg Psychiatry 1998 ; 64 : 344 – 8.en_US
dc.identifier.citedreferenceHenry TR, Leppik IE, Gumnit RJ, Jacobs M. Progressive myoclonus epilepsy treated with zonisamide. Neurology 1988 ; 38 : 928 – 31.en_US
dc.identifier.citedreferenceAwaad Y, Fish I. Baclofen in the treatment of polymyoclonus in a patient with Unverricht-Lundborg disease. J Child Neurol 1995 ; 10 : 68 – 70.en_US
dc.identifier.citedreferenceHurd RW, Wilder BJ, Helveston WR, Uthman BM. Treatment of four siblings with progressive myoclonus epilepsy of the Unverricht-Lundborg type with N -acetylcysteine, Neurology 1996 ; 47 : 1264 – 8.en_US
dc.identifier.citedreferenceHandforth A, DeGiorgio CM, Schachter SC, et al. Vagus nerve stimulation therapy for partial-onset seizures. Neurology 1998 ; 51 : 48 – 55.en_US
dc.identifier.citedreferenceLabar D, Nikolov B, Tarver B, Fraser R. Vagus nerve stimulation for symptomatic generalized epilepsy: a pilot study. Epilepsia 1998 ; 39 : 201 – 5.en_US
dc.identifier.citedreferenceMcLachlan RS. Vagus nerve stimulation for intractable epilepsy. J Clin Neurophysiol 1997 ; 14 : 358 – 68.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.