Huntington's Disease: Two-Year Observational Follow-Up of Executive Function Evaluation with CNS Vital Signs Test in an Adult Patient

Huntington's disease (HD) is a genetic, degenerative, and progressive central nervous system disease. It is characterized by motor abnormalities and cognitive and psychiatric symptoms. Objective. To describe the precise degree of clinical severity of patients with HD through a new neurocognitiv...

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Detalles Bibliográficos
Autores principales: King, Anna Lucia Spear, Valença, Alexandre Martins, e Silva, Adriana Cardoso de Oliveira, Cerqueira, Ana Claudia, Ferraz, Lígia Maria Chaves, Nardi, Antonio Egidio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235665/
https://www.ncbi.nlm.nih.gov/pubmed/22203851
http://dx.doi.org/10.1155/2011/385894

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235665/
https://www.ncbi.nlm.nih.gov/pubmed/22203851
http://dx.doi.org/10.1155/2011/385894

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