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pubmed-article:9827864pubmed:abstractTextThis study was designed to measure ocular movements evoked by galvanic (DC) stimulation using computerised video-oculography. Long duration (>30 s) galvanic vestibular stimulation at currents of up to 5 mA through large-area surface electrodes over the mastoid processes causes maintained changes in the ocular torsional position of both eyes in healthy human subjects. With the subject seated and the head held firmly, torsion was measured by a computer-based image-processing system (VTM). Torsion was recorded in darkness, with or without a single fixation point. With bilateral stimulation, the upper poles of both eyes always torted away from the side of cathode placement and toward the anode. For unilateral stimulation, torsion was directed away from the cathode or toward the anode. The magnitude of ocular torsion was dependent on current strength: with bilateral stimulation the peak torsion was on average 2.88 degrees for 5-mA current intensity compared with 1.58 degrees for 3 mA. A smaller amplitude of torsion was obtained for unilateral stimulation. The average peak torsion was the same for both eyes for all forms of stimulation. Our findings indicate that low-intensity galvanic stimulation evokes ocular torsion in normal subjects, an effect which is consistent with an action on otolith afferents.lld:pubmed
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pubmed-article:9827864pubmed:authorpubmed-author:CurthoysI SISlld:pubmed
pubmed-article:9827864pubmed:authorpubmed-author:WatsonS RSRlld:pubmed
pubmed-article:9827864pubmed:authorpubmed-author:HalmagyiG MGMlld:pubmed
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pubmed-article:9827864pubmed:authorpubmed-author:BrizuelaA EAElld:pubmed
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pubmed-article:9827864pubmed:volume122lld:pubmed
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pubmed-article:9827864pubmed:pagination453-8lld:pubmed
pubmed-article:9827864pubmed:dateRevised2009-11-11lld:pubmed
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pubmed-article:9827864pubmed:year1998lld:pubmed
pubmed-article:9827864pubmed:articleTitleMaintained ocular torsion produced by bilateral and unilateral galvanic (DC) vestibular stimulation in humans.lld:pubmed
pubmed-article:9827864pubmed:affiliationInstitute of Neurological Sciences, Prince of Wales Hospital, Randwick NSW, Sydney, Australia.lld:pubmed
pubmed-article:9827864pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9827864pubmed:publicationTypeClinical Triallld:pubmed
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