Tauopathies, motricité et cognition [Tauopathy, motricity and cognition]

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26 avril 2023

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info:eu-repo/semantics/altIdentifier/doi/10.53738/REVMED.2023.19.824.817

Ce document est lié à :
info:eu-repo/semantics/altIdentifier/pmid/37133943

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info:eu-repo/semantics/altIdentifier/pissn/1660-9379

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info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_FD77DA46AF7D7

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info:eu-repo/semantics/embargoedAccess , Restricted: cannot be viewed until 2024-10-26 , CC BY-NC-ND 4.0 , https://creativecommons.org/licenses/by-nc-nd/4.0/



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H. Kermorvant et al., « Tauopathies, motricité et cognition [Tauopathy, motricity and cognition] », Serveur académique Lausannois, ID : 10.53738/REVMED.2023.19.824.817


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The tauopathies are one of the families of proteinopathies causing neurodegenerative diseases. They are characterized by a combination of cognitive and motor disorders. In this article, we summarize the clinical features of progressive supranuclear palsy and cortico-basal degeneration, focusing on their cognitive-behavioral impairment profiles, which in some cases allow them to be differentiated from other neurodegenerative entities. Finally, we propose tools for therapeutic management.

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