In vivo diagnosis of TDP-43 proteinopathies: in search of biomarkers of clinical use

Abstract TDP-43 proteinopathies are a heterogeneous group of neurodegenerative disorders that share the presence of aberrant, misfolded and mislocalized deposits of the protein TDP-43, as in the case of amyotrophic lateral sclerosis and some, but not all, pathological variants of frontotemporal deme...

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Bibliographic Details
Published in:Translational Neurodegeneration
Main Authors: Juan I. López-Carbonero, Irene García-Toledo, Laura Fernández-Hernández, Pablo Bascuñana, María J. Gil-Moreno, Jordi A. Matías-Guiu, Silvia Corrochano
Format: Article
Language:English
Published: BMC 2024-06-01
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Online Access:https://doi.org/10.1186/s40035-024-00419-8