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Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 27, 2005
Comparison of two percutaneous radiological gastrostomy tubes in the nutritional management of ALS patientsAlan Rio, Mary Ann Ampong, Martin R Turner, et al.
Alzheimer'S Research & Therapy|December 9, 2014
Imaging as a biomarker in drug discovery for Alzheimer's disease: is MRI a suitable technology?Emilio Merlo Pich, Andreas Jeromin, Giovanni B Frisoni, et al.
Neurobiology of Aging|May 11, 2012
Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosisYevgeniya Abramzon, Janel O Johnson, Sonja W Scholz, et al.
Acta Neuropathologica Communications|August 19, 2025
TDP-43 pathology is associated with divergent protein profiles in ALS brain and spinal cordEmily Feneberg, Alexander G Thompson, Philip D Charles, et al.
Brain Pathology (Zurich, Switzerland)|December 10, 2020
Detection and quantification of novel C-terminal TDP-43 fragments in ALS-TDPEmily Feneberg, Philip D Charles, Mattéa J Finelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 28, 2014
Use of clinical staging in amyotrophic lateral sclerosis for phase 3 clinical trialsRubika Balendra, Ashley Jones, Naheed Jivraj, et al.
The New England Journal of Medicine|April 9, 2025
A Phase 3 Trial of Inebilizumab in Generalized Myasthenia GravisRichard J Nowak, Michael Benatar, Emma Ciafaloni, et al.
Annals of Clinical and Translational Neurology|December 8, 2023
Subcutaneous batoclimab in generalized myasthenia gravis: Results from a Phase 2a trial with an open-label extensionRichard J Nowak, Ari Breiner, Vera Bril, et al.
AJNR. American Journal of Neuroradiology|September 18, 2025
Progressive and short-interval changes observed in the corticospinal tract and corpus callosum of ALS patients: A texture analysis studyPedram Parnianpour, Matthew Harrison, Michael Benatar, et al.
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