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Journal of the Neurological Sciences|December 19, 2017
History and current difficulties in classifying inherited myopathies and muscular dystrophiesStéphane Mathis, Meriem Tazir, Laurent Magy, et al.
European Journal of Epidemiology|September 13, 2022
Spatio-temporal clustering of amyotrophic lateral sclerosis in France: A population-based studyFarid Boumédiene, Benoît Marin, Jaime Luna, et al.
Dementia and Geriatric Cognitive Disorders|April 24, 2018
Predictors of Rapid Cognitive Decline in Patients with Mild-to-Moderate Alzheimer Disease: A Prospective Cohort Study with 12-Month Follow-Up Performed in Memory ClinicsAchille E Tchalla, Jean-Pierre Clément, Isabelle Saulnier, et al.
International Journal of Molecular Sciences|January 21, 2023
Study of Ubiquitin Pathway Genes in a French Population with Amyotrophic Lateral Sclerosis: Focus on <i>HECW1</i> Encoding the E3 Ligase NEDL1Shanez Haouari, Christian Robert Andres, Debora Lanznaster, et al.
Nutrition (Burbank, Los Angeles County, Calif.)|May 7, 2020
Increased resting energy expenditure compared with predictive theoretical equations in amyotrophic lateral sclerosisPierre Jésus, Philippe Fayemendy, Benoit Marin, et al.
Molecular Neurobiology|March 1, 2017
Liver X Receptor Genes Variants Modulate ALS PhenotypeKevin Mouzat, Nicolas Molinari, Jovana Kantar, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 26, 2018
Neurite density is reduced in the presymptomatic phase of <i>C9orf72</i> diseaseJunhao Wen, Hui Zhang, Daniel C Alexander, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 2, 2018
Phenotypic and genotypic studies of ALS cases in ALS-SMA familiesPhilippe Corcia, Patrick Vourc'h, Helene Blasco, et al.
Journal of Alzheimer'S Disease : JAD|December 16, 2010
Memantine in behavioral variant frontotemporal dementia: negative resultsMartine Vercelletto, Claire Boutoleau-Bretonnière, Christelle Volteau, et al.
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