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2016-01-05

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cc-by (c) Brito, Verónica; Ginés Padrós, Silvia, 2016
Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/119016

p75NTR in Huntington's disease: beyond the basal ganglia

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https://doi.org/10.18632/oncotarget.6646

Abstract

Huntington’s disease (HD) is a fatal neurodegenerative disorder with a characteristic phenotype including chorea and dystonia, uncoordinated fine movements, cognitive decline and psychiatric disturbances. Even though the clinical diagnosis of HD relies on the manifestation of motor abnormalities, the associated memory impairments have been growing in prominence. Indeed, cognitive deficits are evident along all the disease process even in the prodrome before any motor diagnosis is given.

Subject

Corea de Huntington, Malalties neurodegeneratives, Ganglis basals, Hipocamp (Cervell)

Subject (English)

Huntington's chorea, Neurodegenerative Diseases, Basal ganglia, Hippocampus (Brain)

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Articles publicats en revistes (Biomedicina)
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)

Citation

BRITO, Verónica and GINÉS PADRÓS, Silvia. p75NTR in Huntington's disease: beyond the basal ganglia. Oncotarget. 2016. Vol. 7, num. 1. ISSN 1949-2553. [consulted: 7 of August of 2026]. Available at: https://hdl.handle.net/2445/119016

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