2004
DOI: 10.1007/s00415-004-0378-3
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The diagnostic value of vestibular evoked myogenic potentials in multiple sclerosis

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Cited by 54 publications
(35 citation statements)
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“…cVEMP abnormalities were reported in multiple sclerosis (MS) patients. It has been determined that increases in p13 and n23 latencies may be secondary to demyelination of the vestibulo-spinal pathway [28][29][30][31][32] .…”
Section: Discussionmentioning
confidence: 99%
“…cVEMP abnormalities were reported in multiple sclerosis (MS) patients. It has been determined that increases in p13 and n23 latencies may be secondary to demyelination of the vestibulo-spinal pathway [28][29][30][31][32] .…”
Section: Discussionmentioning
confidence: 99%
“…Limits of normal values were obtained by adding 2.5 SD to the mean latency and amplitude values of our laboratory. 26,27 Statistical analysis Both eyes of each patient were included in the study. The ON eyes were compared to the normal database of the instruments and to the unaffected fellow eye.…”
Section: Visual Evoked Potentialmentioning
confidence: 99%
“…Prolonged VEMPs could be due to demyelination from either of primary afferent axons at the root entry zone or secondary vestibulospinal tract axons rather than to lesions involving vestibular nucleus [47][48][49]. Measurement of VEMPs is therefore helpful in detecting subclinical vestibulospinal lesions in suspected multiple sclerosis [50].…”
Section: Central Vestibular Lesionsmentioning
confidence: 99%