Please use this identifier to cite or link to this item:
Title: p75NTR in Huntington's disease: beyond the basal ganglia
Author: Brito, Verónica
Ginés Padrós, Silvia
Keywords: Corea de Huntington
Malalties neurodegeneratives
Ganglis basals
Hipocamp (Cervell)
Huntington's chorea
Neurodegenerative diseases
Basal ganglia
Hippocampus (Brain)
Issue Date: 5-Jan-2016
Publisher: Impact Journals
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.
Note: Reproducció del document publicat a:
It is part of: Oncotarget, 2016, vol. 7, num. 1
Related resource:
ISSN: 1949-2553
Appears in Collections:Articles publicats en revistes (Biomedicina)
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)

Files in This Item:
File Description SizeFormat 
658966.pdf510.88 kBAdobe PDFView/Open

This item is licensed under a Creative Commons License Creative Commons