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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|January 5, 2013
Non-invasive ventilation in amyotrophic lateral sclerosisBart Vrijsen, Dries Testelmans, Catharina Belge, et al.Journal of Neuropathology and Experimental Neurology|July 27, 2005
GluR2 deficiency accelerates motor neuron degeneration in a mouse model of amyotrophic lateral sclerosisPhilip Van Damme, Dries Braeken, Geert Callewaert, et al.Neurobiology of Aging|April 24, 2013
Progranulin does not affect motor neuron degeneration in mutant SOD1 mice and ratsSarah Herdewyn, Louis De Muynck, Ludo Van Den Bosch, et al.Journal of Neuropathology and Experimental Neurology|November 15, 2002
Upregulation of HSP27 in a transgenic model of ALSVicky Vleminckx, Philip Van Damme, Karolien Goffin, et al.Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|March 5, 2016
Prospective Validation of 18F-FDG Brain PET Discriminant Analysis Methods in the Diagnosis of Amyotrophic Lateral SclerosisDonatienne Van Weehaeghe, Jenny Ceccarini, Aline Delva, et al.Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|March 14, 2015
Noninvasive ventilation improves sleep in amyotrophic lateral sclerosis: a prospective polysomnographic studyBart Vrijsen, Bertien Buyse, Catharina Belge, et al.Molecular Neurodegeneration|June 19, 2014
Prevention of intestinal obstruction reveals progressive neurodegeneration in mutant TDP-43 (A315T) miceSarah Herdewyn, Carla Cirillo, Ludo Van Den Bosch, et al.Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|December 14, 2016
Development of Improved HDAC6 Inhibitors as Pharmacological Therapy for Axonal Charcot-Marie-Tooth DiseaseVeronick Benoy, Pieter Vanden Berghe, Matthew Jarpe, et al.European Journal of Human Genetics : EJHG|October 10, 2013
Exome sequencing reveals HINT1 mutations as a cause of distal hereditary motor neuropathyHui Zhao, Valérie Race, Gert Matthijs, et al.Neurobiology of Aging|April 25, 2018
Conditional deletion of Id2 or Notch1 in oligodendrocyte progenitor cells does not ameliorate disease outcome in SOD1<sup>G93A</sup> miceCaroline Eykens, Annelies Nonneman, Cathy Jensen, et al.Pageof 37