p75NTR in Huntington's disease: beyond the basal ganglia

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, th...

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Detalhes bibliográficos
Autores: Brito, Verónica, Ginés Padrós, Silvia
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2016
País:España
Recursos:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/119016
Acesso em linha:https://hdl.handle.net/2445/119016
Access Level:acceso abierto
Palavra-chave:Corea de Huntington
Malalties neurodegeneratives
Ganglis basals
Hipocamp (Cervell)
Huntington's chorea
Neurodegenerative Diseases
Basal ganglia
Hippocampus (Brain)
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spelling p75NTR in Huntington's disease: beyond the basal gangliaBrito, VerónicaGinés Padrós, SilviaCorea de HuntingtonMalalties neurodegenerativesGanglis basalsHipocamp (Cervell)Huntington's choreaNeurodegenerative DiseasesBasal gangliaHippocampus (Brain)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.Impact Journals2018201820162018info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion2 p.application/pdfhttps://hdl.handle.net/2445/119016Articles publicats en revistes (Biomedicina)reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésReproducció del document publicat a: https://doi.org/10.18632/oncotarget.6646Oncotarget, 2016, vol. 7, num. 1https://doi.org/10.18632/oncotarget.6646cc-by (c) Brito, Verónica; Ginés Padrós, Silvia, 2016http://creativecommons.org/licenses/by/3.0/esinfo:eu-repo/semantics/openAccessoai:recercat.cat:2445/1190162026-05-29T05:05:01Z
dc.title.none.fl_str_mv p75NTR in Huntington's disease: beyond the basal ganglia
title p75NTR in Huntington's disease: beyond the basal ganglia
spellingShingle p75NTR in Huntington's disease: beyond the basal ganglia
Brito, Verónica
Corea de Huntington
Malalties neurodegeneratives
Ganglis basals
Hipocamp (Cervell)
Huntington's chorea
Neurodegenerative Diseases
Basal ganglia
Hippocampus (Brain)
title_short p75NTR in Huntington's disease: beyond the basal ganglia
title_full p75NTR in Huntington's disease: beyond the basal ganglia
title_fullStr p75NTR in Huntington's disease: beyond the basal ganglia
title_full_unstemmed p75NTR in Huntington's disease: beyond the basal ganglia
title_sort p75NTR in Huntington's disease: beyond the basal ganglia
dc.creator.none.fl_str_mv Brito, Verónica
Ginés Padrós, Silvia
author Brito, Verónica
author_facet Brito, Verónica
Ginés Padrós, Silvia
author_role author
author2 Ginés Padrós, Silvia
author2_role author
dc.subject.none.fl_str_mv Corea de Huntington
Malalties neurodegeneratives
Ganglis basals
Hipocamp (Cervell)
Huntington's chorea
Neurodegenerative Diseases
Basal ganglia
Hippocampus (Brain)
topic Corea de Huntington
Malalties neurodegeneratives
Ganglis basals
Hipocamp (Cervell)
Huntington's chorea
Neurodegenerative Diseases
Basal ganglia
Hippocampus (Brain)
description 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.
publishDate 2016
dc.date.none.fl_str_mv 2016
2018
2018
2018
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://hdl.handle.net/2445/119016
url https://hdl.handle.net/2445/119016
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv Reproducció del document publicat a: https://doi.org/10.18632/oncotarget.6646
Oncotarget, 2016, vol. 7, num. 1
https://doi.org/10.18632/oncotarget.6646
dc.rights.none.fl_str_mv cc-by (c) Brito, Verónica; Ginés Padrós, Silvia, 2016
http://creativecommons.org/licenses/by/3.0/es
info:eu-repo/semantics/openAccess
rights_invalid_str_mv cc-by (c) Brito, Verónica; Ginés Padrós, Silvia, 2016
http://creativecommons.org/licenses/by/3.0/es
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 2 p.
application/pdf
dc.publisher.none.fl_str_mv Impact Journals
publisher.none.fl_str_mv Impact Journals
dc.source.none.fl_str_mv Articles publicats en revistes (Biomedicina)
reponame:Recercat. Dipósit de la Recerca de Catalunya
instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
instname_str Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
reponame_str Recercat. Dipósit de la Recerca de Catalunya
collection Recercat. Dipósit de la Recerca de Catalunya
repository.name.fl_str_mv
repository.mail.fl_str_mv
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score 15,81155

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