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Journal of the Neurological Sciences|July 12, 2005
Frequency of a tau genotype in amyotrophic lateral sclerosisChristoph Münch, Florian Prechter, Renshi Xu, et al.Journal of Neurology|September 15, 2023
Impairment of oculomotor functions in patients with early to advanced amyotrophic lateral sclerosisElisa Aust, Sven-Thomas Graupner, René Günther, et al.Neuro-Degenerative Diseases|November 28, 2015
No Change in Executive Performance in ALS Patients: A Longitudinal Neuropsychological StudyElisabeth Kasper, Kolja Zydatiss, Christina Schuster, et al.Frontiers in Neuroscience|July 12, 2021
Cognitive Profiles of Amyotrophic Lateral Sclerosis Differ in Resting-State Functional Connectivity: An fMRI StudyAnna G M Temp, Martin Dyrba, Charlotte Büttner, et al.Frontiers in Molecular Neuroscience|October 30, 2016
Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS CohortStefanie Krüger, Florian Battke, Andrea Sprecher, et al.Neurobiology of Aging|August 16, 2012
Screening in ALS and FTD patients reveals 3 novel UBQLN2 mutations outside the PXX domain and a pure FTD phenotypeMatthis Synofzik, Walter Maetzler, Torsten Grehl, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 11, 2025
Prospective Multicenter Evaluation of the MDS "Suggestive of PSP" Diagnostic CriteriaAndrea Quattrone, Nicolai Franzmeier, Johannes Levin, et al.Neuroimage. Clinical|June 8, 2018
Prefrontal cortical thickness in motor neuron diseaseJudith Machts, Arturo Cardenas-Blanco, Julio Acosta-Cabronero, et al.Neurobiology of Aging|September 3, 2013
Cortical thinning and its relation to cognition in amyotrophic lateral sclerosisChristina Schuster, Elisabeth Kasper, Martin Dyrba, et al.Journal of Neurology|July 5, 2022
Quality of life and mental health in the locked-in-state-differences between patients with amyotrophic lateral sclerosis and their next of kinElisa Aust, Katharina Linse, Sven-Thomas Graupner, et al.Pageof 11