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BMJ Open|September 3, 2014
Searching for a link between the L-BMAA neurotoxin and amyotrophic lateral sclerosis: a study protocol of the French BMAALS programmeAurélie Delzor, Philippe Couratier, Farid Boumédiène, et al.Neurobiology of Disease|July 13, 2024
Caffeine consumption outcomes on amyotrophic lateral sclerosis disease progression and cognitionVincent Huin, David Blum, Violette Delforge, et al.Journal of Parkinson'S Disease|February 20, 2025
Therapeutic modalities of deferiprone in Parkinson's disease: SKY and EMBARK studiesDavid Devos, Olivier Rascol, Wassilios G Meissner, et al.BMJ Neurology Open|February 23, 2026
Bi-allelic intermediate ATXN2 repeat expansions are associated with slow progressing, leg-onset familial ALSKoen Cedric Demaegd, Wouter Koole, Joke Jfa van Vugt, et al.Neurobiology of Aging|March 16, 2020
Plasma progranulin levels for frontotemporal dementia in clinical practice: a 10-year French experienceLeila Sellami, Benoît Rucheton, Imen Ben Younes, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 7, 2021
Effect of familial clustering in the genetic screening of 235 French ALS familiesPhilippe Corcia, William Camu, Celine Brulard, et al.JAMA Neurology|March 24, 2025
Reldesemtiv in Amyotrophic Lateral Sclerosis: Results From the COURAGE-ALS Randomized Clinical TrialJeremy M Shefner, Merit E Cudkowicz, Angela Genge, et al.Annals of Clinical and Translational Neurology|May 22, 2024
Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALSHeather Marriott, Thomas P Spargo, Ahmad Al Khleifat, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 12, 2025
Hospitalizations as an outcome measure in COURAGE-ALSStacy A Rudnicki, Ammar Al-Chalabi, Jinsy A Andrews, et al.Journal of Alzheimer'S Disease : JAD|December 21, 2012
C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testingIsabelle Le Ber, Agnès Camuzat, Lena Guillot-Noel, et al.Pageof 13