1987
DOI: 10.1016/0168-5597(87)90024-4
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Delayed visual evoked potentials are independent of pattern orientation in macular disease

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Cited by 18 publications
(10 citation statements)
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“…This finding implies cortical pathology because the receptive field of retinal cells is circular or oval (86) and therefore these cells do not have a significant response preference for one orientation or another. The VEPs of patients with macular degeneration are slowed but are not sensitive to sine wave grating orientation (87), further supporting the hypothesis that cortical pathology underlies the sensitivity to orientation, as the retina is the site of the lesion in macular degeneration. These findings indicate that VEPs using sine wave grating and visual contrast sensitivity studies can be used to localize pathology in the visual system of patients exposed to Pfiesteria and that localization of the pathology will depend on the response to orientation of the grating stimulus.…”
Section: Directions For Future Researchconfirming and Extending Priorsupporting
confidence: 57%
“…This finding implies cortical pathology because the receptive field of retinal cells is circular or oval (86) and therefore these cells do not have a significant response preference for one orientation or another. The VEPs of patients with macular degeneration are slowed but are not sensitive to sine wave grating orientation (87), further supporting the hypothesis that cortical pathology underlies the sensitivity to orientation, as the retina is the site of the lesion in macular degeneration. These findings indicate that VEPs using sine wave grating and visual contrast sensitivity studies can be used to localize pathology in the visual system of patients exposed to Pfiesteria and that localization of the pathology will depend on the response to orientation of the grating stimulus.…”
Section: Directions For Future Researchconfirming and Extending Priorsupporting
confidence: 57%
“…However, studies of retinal or optic nerve diseases have indicated that the PERG alteration is not necessarily limited to its amplitude but may also be reflected in changes of peak-time, namely, in cases of retinal disorders [11,12]. Meanwhile, there is an increasing number of reports on VECP delays in patients with pure retinal disorders such as X-linked juvenile retinoschisis [17], Stargardt's disease [8], central serous retinopathy [10,[18][19][20] and macular holes [9,21]. All of these authors have concluded that a delayed VECP cannot be considered specific for postretinal neuropathies (eg, demyelinating diseases), and the present data support their view.…”
Section: Discussionmentioning
confidence: 99%
“…Some uncertainty and controversy still remains, however, about the origin of VECP delays in retinal diseases. Lennerstrand [8], Bass and associates [9] and Bodis-Wollner and colleagues [20] have discussed the development of a concomitant optic neuropathy responsible for the VECP delay. Usually the authors excluded this possibility based on ophthalmoscopic inspection of the optic disc [20] or the time course of retinal diseases being too short to allow an anterograde degeneration of neuronal structures [8,20].…”
Section: Discussionmentioning
confidence: 99%
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“…19,51 Retinitis pigmentosa is a disease entity in which the rods and cones progressively degenerate. However, the integrity of the VEP does depend on the integrity of the ganglion cells.…”
Section: Retinal Lesionsmentioning
confidence: 99%