Retinal fingerprints of ALS in patients: Ganglion cell apoptosis and TDP-43/p62 misplacement
IntroductionAmyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by the progressive loss of motor neuron function. Although ophthalmic deficits are not considered a classic symptom of ALS, recent studies suggest that changes in retinal cells, similar to those in the...
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| Váldodahkkit: | , , , , , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Frontiers Media S.A.
2023-03-01
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| Ráidu: | Frontiers in Aging Neuroscience |
| Fáttát: | |
| Liŋkkat: | https://www.frontiersin.org/articles/10.3389/fnagi.2023.1110520/full |
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