Involvement of Foxp2 in the alterations of the basal ganglia circuitry in Huntington’s Disease

Autor: Rodríguez Urgellés, Ened

Publikováno v: TDX (Tesis Doctorals en Xarxa)
TDR. Tesis Doctorales en Red
instname
Dipòsit Digital de la UB
Universidad de Barcelona

[eng] Huntington’s Disease (HD) is an autosomal dominant inherited neurodegenerative disorder characterized by motor, psychiatric, and cognitive manifestations. The disease is caused by an unstable expansion of the CAG trinucleotide repeat in the h

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2fcda88b342de403118c9ec32de645a1
http://hdl.handle.net/10803/674550

A systematic linguistic profile of spontaneous narrative speech in pre-symptomatic and early stage Huntington's disease

Autor: Clara Garcia-Gorro, Raymond Salvador, Wolfram Hinzen, Ruth de Diego-Balaguer, Joana Rosselló, Cati Morey, Estela Camara

Publikováno v: Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior

Cognitive decline accompanying the clinically more salient motor symptoms of Hunting- ton's disease (HD) has been widely noted and can precede motor symptoms onset. Less clear is how such decline bears on language functions in everyday life, though a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d037d63494bf197371f26f51279b1750
https://doi.org/10.1016/j.cortex.2017.07.022

p75NTR in Huntington's disease: beyond the basal ganglia

Autor: Verónica Brito, Silvia Ginés

Publikováno v: Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Oncotarget

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 reli

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27e7b23231986439d8d7fbb40aadc37b
http://hdl.handle.net/2445/119016

Gene therapy as a treatment for Huntington's disease

Autor: Costa Verdera, Helena, Universitat Autònoma de Barcelona. Facultat de Biociències

Publikováno v: Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9a2a018ef2674c763957fccb2ce7cdfd
https://ddd.uab.cat/record/119275

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

Autor: Jon E. Berner, Olga Carmona, Bala V. Manyam, Martin Paucar, Henry Brodaty, Giovanni Coppola, Henry L. Paulson, Milena Jankovic, Melissa K. Maisenbacher, John C. Adair, Janice M. Fullerton, Alden Y. Huang, Renee L. Sears, Serge Jaumà, Joanna C. Jen, Joerg Klepper, John L. Goudreau, Jerrold L. Vitek, Daniel H. Geschwind, Beatriz Quintáns, Elizabeth Spiteri, Witoon Mitarnun, Per Svenningsson, Charles A. Williams, Mayana Zatz, Sheila A Simpson, Daniel García-Estevez, Philip B. Mitchell, João Ricardo Mendes de Oliveira, Vladimir S. Kostic, Sandy Chan Hsu, Peter R. Schofield, Jill Goldman, Brent L. Fogel, R. R. Lemos, Michele Yang, Catherine Mamah, Ivana Novakovic, Lisette Nevarez, Pietro Mazzoni, Z. Miedzybrodzka, Agnès Linglart, Paul J. Tuite, Kerrie D. Pierce, Suppachok Wetchaphanphesat, María Jesús Sobrido, Jennifer Mueller, Anthony E. Lang, Matthew Bower, Valerija Dobricic, Suppachok Kirdlarp, Suellen Hopfer

Publikováno v: Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

Familial idiopathic basal ganglia calcification (IBGC) or Fahr's disease is a rare neurodegenerative disorder characterized by calcium deposits in the basal ganglia and other brain regions, which is associated with neuropsychiatric and motor symptoms

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99acc47edc2ffba13fc014d89bb4073c
http://hdl.handle.net/2445/126473