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Please use this identifier to cite or link to this item: http://dspace.bsu.edu.ru/handle/123456789/52025
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dc.contributor.authorSoldatov, V. O.-
dc.contributor.authorKukharsky, M. S.-
dc.contributor.authorBelykh, A. E.-
dc.contributor.authorSobolev, A. M.-
dc.contributor.authorDeykin, A. V.-
dc.date.accessioned2023-03-03T07:49:44Z-
dc.date.available2023-03-03T07:49:44Z-
dc.date.issued2021-
dc.identifier.citationRetinal damage in amyotrophic lateral sclerosis: underlying mechanisms / V.O. Soldatov [et al.] // Eye and Brain. - 2021. - Vol.13.-P. 131-146.ru
dc.identifier.urihttp://dspace.bsu.edu.ru/handle/123456789/52025-
dc.description.abstractAmyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease resulting in a gradual loss of motor neuron function. Although ophthalmic complaints are not presently considered a classic symptom of ALS, retinal changes such as thinning, axonal degeneration and inclusion bodies have been found in many patientsru
dc.language.isoenru
dc.subjectmedicineru
dc.subjectophthalmologyru
dc.subjectretinaru
dc.subjectretinal involvementru
dc.subjectneuro-ophthalmologyru
dc.subjectmitochondrial dysfunctionru
dc.subjectexcitotoxicityru
dc.titleRetinal damage in amyotrophic lateral sclerosis: underlying mechanismsru
dc.typeArticleru
Appears in Collections:Статьи из периодических изданий и сборников (на иностранных языках) = Articles from periodicals and collections (in foreign languages)

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