{"title":"视网膜神经节细胞功能临床检测的新进展","authors":"M. Bearse, E. Sutter, A. Palmowski","doi":"10.1364/vsia.1997.mb.4","DOIUrl":null,"url":null,"abstract":"We recently developed a method for extracting a component from the human multifocal electroretinogram (ERG) that is generated by ganglion cells1,2. As its latency depends linearly on the estimated length of ganglion cell axons connecting the site of focal stimulation with the disc, this optic nerve head component (ONHC) is presumed to originate from the axons where myelination begins1,2. A second, retinal component (RC) has an invariant latency.","PeriodicalId":428257,"journal":{"name":"Vision Science and its Applications","volume":"282 5 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"17","resultStr":"{\"title\":\"New Developments toward a Clinical Test of Retinal Ganglion Cell Function\",\"authors\":\"M. Bearse, E. Sutter, A. Palmowski\",\"doi\":\"10.1364/vsia.1997.mb.4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We recently developed a method for extracting a component from the human multifocal electroretinogram (ERG) that is generated by ganglion cells1,2. As its latency depends linearly on the estimated length of ganglion cell axons connecting the site of focal stimulation with the disc, this optic nerve head component (ONHC) is presumed to originate from the axons where myelination begins1,2. A second, retinal component (RC) has an invariant latency.\",\"PeriodicalId\":428257,\"journal\":{\"name\":\"Vision Science and its Applications\",\"volume\":\"282 5 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"17\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Vision Science and its Applications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1364/vsia.1997.mb.4\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vision Science and its Applications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1364/vsia.1997.mb.4","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
New Developments toward a Clinical Test of Retinal Ganglion Cell Function
We recently developed a method for extracting a component from the human multifocal electroretinogram (ERG) that is generated by ganglion cells1,2. As its latency depends linearly on the estimated length of ganglion cell axons connecting the site of focal stimulation with the disc, this optic nerve head component (ONHC) is presumed to originate from the axons where myelination begins1,2. A second, retinal component (RC) has an invariant latency.
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