Retinal fingerprints of ALS in patients: Ganglion cell apoptosis and TDP-43/p62 misplacement

INTRODUCTION: Amyotrophic 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 t...

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Detalles Bibliográficos
Autores principales: Pediconi, Natalia, Gigante, Ylenia, Cama, Silvia, Pitea, Martina, Mautone, Lorenza, Ruocco, Giancarlo, Ghirga, Silvia, Di Angelantonio, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Aging Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061015/
https://www.ncbi.nlm.nih.gov/pubmed/37009460
http://dx.doi.org/10.3389/fnagi.2023.1110520

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061015/
https://www.ncbi.nlm.nih.gov/pubmed/37009460
http://dx.doi.org/10.3389/fnagi.2023.1110520

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