Cargando…
A systematic review of non-motor symptom evaluation in clinical trials for amyotrophic lateral sclerosis
BACKGROUND: Amyotrophic lateral sclerosis (ALS) is increasingly recognised as a multi-system disorder, presenting with common and impactful non-motor symptoms, such as neuropsychiatric symtpoms, cognitive and behavioural changes, pain, disordered sleep, fatigue and problematic saliva. AIM/HYPOTHESIS...
Autores principales: | Beswick, Emily, Forbes, Deborah, Hassan, Zack, Wong, Charis, Newton, Judith, Carson, Alan, Abrahams, Sharon, Chandran, Siddharthan, Pal, Suvankar |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8738361/ https://www.ncbi.nlm.nih.gov/pubmed/34120226 http://dx.doi.org/10.1007/s00415-021-10651-1 |
Ejemplares similares
-
A systematic review of neuropsychiatric and cognitive assessments used in clinical trials for amyotrophic lateral sclerosis
por: Beswick, Emily, et al.
Publicado: (2020) -
A systematic review of digital technology to evaluate motor function and disease progression in motor neuron disease
por: Beswick, Emily, et al.
Publicado: (2022) -
Riluzole prescribing, uptake and treatment discontinuation in people with amyotrophic lateral sclerosis in Scotland
por: Jayaprakash, Kiran, et al.
Publicado: (2020) -
Prospective observational cohort study of factors influencing trial participation in people with motor neuron disease (FIT-participation-MND): a protocol
por: Beswick, Emily, et al.
Publicado: (2021) -
Cerebrospinal fluid cytotoxicity in amyotrophic lateral sclerosis: a systematic review of in vitro studies
por: Ng Kee Kwong, Koy Chong, et al.
Publicado: (2020)