Items where authors include "Chaouch, A."

Article

Young, C.A. orcid.org/0000-0003-1745-7720, Chaouch, A., Mcdermott, C.J. orcid.org/0000-0002-1269-9053 et al. (8 more authors) (2025) Fatigue in amyotrophic lateral sclerosis/motor neuron disease: prevalence, influences and trajectories. Amyotrophic lateral sclerosis and frontotemporal degeneration. ISSN 2167-8421

Young, C.A. orcid.org/0000-0003-1745-7720, Chaouch, A., Mcdermott, C.J. orcid.org/0000-0002-1269-9053 et al. (6 more authors) (2025) Patient reported outcome measures require scale metrification and quantified precision: evidence from the assessment of breathlessness in people with ALS/MND. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. ISSN 2167-8421

Musson, L.S. orcid.org/0000-0002-1246-2734, Mitic, N. orcid.org/0009-0002-5397-0206, Leigh-Valero, V. orcid.org/0009-0008-3413-8741 et al. (15 more authors) (2025) The use of digital devices to monitor physical behavior in motor neuron disease: systematic review. Journal of Medical Internet Research, 27. e68479. ISSN 1438-8871

Young, C.A. orcid.org/0000-0003-1745-7720, Chaouch, A., Mcdermott, C.J. orcid.org/0000-0002-1269-9053 et al. (12 more authors) (2025) Determinants and progression of stigma in amyotrophic lateral sclerosis/motor neuron disease. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 26 (3-4). pp. 192-202. ISSN 2167-8421

Howard, J. orcid.org/0000-0001-7182-593X, Chaouch, A. orcid.org/0009-0005-4340-6400, Douglas, A.G.L. et al. (3 more authors) (2025) Genetic testing for monogenic forms of motor neuron disease/amyotrophic lateral sclerosis in unaffected family members. European Journal of Human Genetics, 33 (1). pp. 7-13. ISSN 1018-4813

Young, C.A. orcid.org/0000-0003-1745-7720, Chaouch, A., Mcdermott, C.J. orcid.org/0000-0002-1269-9053 et al. (6 more authors) (2024) Improving the measurement properties of the amyotrophic lateral sclerosis functional rating scale-revised (ALSFRS-R): deriving a valid measurement total for the calculation of change. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 25 (3-4). pp. 400-409. ISSN 2167-8421

Young, C.A. orcid.org/0000-0003-1745-7720, Chaouch, A., Mcdermott, C.J. orcid.org/0000-0002-1269-9053 et al. (10 more authors) (2024) Dyspnea (breathlessness) in amyotrophic lateral sclerosis/motor neuron disease: prevalence, progression, severity, and correlates. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. pp. 1-11. ISSN 2167-8421

Lombardo, F.L. orcid.org/0000-0001-6183-0735, Spila Alegiani, S., Mayer, F. et al. (93 more authors) (2023) A randomized double-blind clinical trial on safety and efficacy of tauroursodeoxycholic acid (TUDCA) as add-on treatment in patients affected by amyotrophic lateral sclerosis (ALS): the statistical analysis plan of TUDCA-ALS trial. Trials, 24 (1). 792. ISSN 1468-6708

Saxon, J.A., Thompson, J.C., Harris, J.M. et al. (11 more authors) (2020) The Edinburgh Cognitive and Behavioral ALS Screen (ECAS) in frontotemporal dementia. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 21 (7-8). pp. 606-613. ISSN 2167-8421