Comorbidities and clinical outcomes in adult- and juvenile-onset Huntington’s disease: a study of linked Swedish National Registries (2002–2019)

BACKGROUND: Huntington’s disease (HD) is a rare, neurodegenerative disease and its complex motor, cognitive and psychiatric symptoms exert a lifelong clinical burden on both patients and their families. OBJECTIVE: To describe the clinical burden and natural history of HD. METHODS: This longitudinal...

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Detalles Bibliográficos
Autores principales: Furby, Hannah, Moore, Suzanne, Nordstroem, Anna-Lena, Houghton, Richard, Lambrelli, Dimitra, Graham, Sophie, Svenningsson, Per, Petersén, Åsa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Original Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9886595/
https://www.ncbi.nlm.nih.gov/pubmed/36253622
http://dx.doi.org/10.1007/s00415-022-11418-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9886595/
https://www.ncbi.nlm.nih.gov/pubmed/36253622
http://dx.doi.org/10.1007/s00415-022-11418-y

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