Autonomic dysfunction is associated with disease progression and survival in amyotrophic lateral sclerosis: a prospective longitudinal cohort study

BACKGROUND: Among non-motor symptoms, autonomic disturbances have been described in amyotrophic lateral sclerosis (ALS) and reported as mild to moderate in up to 75% of patients. However, no study has systematically investigated autonomic symptoms as prognostic factors. OBJECTIVES: The main aim of t...

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Detalles Bibliográficos
Autores principales: Dubbioso, Raffaele, Provitera, Vincenzo, Pacella, Daniela, Santoro, Lucio, Manganelli, Fiore, Nolano, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Original Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511550/
https://www.ncbi.nlm.nih.gov/pubmed/37358634
http://dx.doi.org/10.1007/s00415-023-11832-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511550/
https://www.ncbi.nlm.nih.gov/pubmed/37358634
http://dx.doi.org/10.1007/s00415-023-11832-w

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