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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 9, 2026
18F FDG-PET correlates of motor neuron disease motor variantsBoris Deleu, Patrick Dupont, Kato Bracaval, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 31, 2023
COURAGE-ALS: a randomized, double-blind phase 3 study designed to improve participant experience and increase the probability of successJeremy M Shefner, Ammar Al-Chalabi, Jinsy A Andrews, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 2, 2019
Telomere length is greater in ALS than in controls: a whole genome sequencing studyAhmad Al Khleifat, Alfredo Iacoangeli, Aleksey Shatunov, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 5, 2023
Predicting amyotrophic lateral sclerosis (ALS) progression with machine learningMuzammil Arif Din Abdul Jabbar, Ling Guo, Sonakshi Nag, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|November 9, 2012
Premorbid body mass index and risk of amyotrophic lateral sclerosisÉilis J O'Reilly, Hao Wang, Marc G Weisskopf, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 29, 2026
Diagnostic differences between military veterans and non-veterans: data from the United States National ALS RegistryJaime Raymond, Theodore Larson, Suraya Mohidul, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 23, 2021
Mortality among family members of patients with amyotrophic lateral sclerosis - a Swedish register-based studyUlf Kläppe, Elisa Longinetti, Henrik Larsson, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|January 5, 2013
Familial amyotrophic lateral sclerosis in Alberta, CanadaTed Pfister, Ramnik Sekhon, Mitchell White, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 16, 2026
Dysphagia in behavioural variant of frontotemporal dementia- a systematic reviewElishka S Bailey, Alayna Rowell, Rachel MulherenAmyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 16, 2026
Emerging strategies for interpreting variants of uncertain significance (VUS) in amyotrophic lateral sclerosisMinhal Ahmed, Kathryn Volkening, Crystal Mclellan, et al.Pageof 125