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JAMA Neurology|March 12, 2014
Value of 18fluorodeoxyglucose-positron-emission tomography in amyotrophic lateral sclerosis: a prospective studyKoen Van Laere, Annelies Vanhee, Jolien Verschueren, et al.Critical Care (London, England)|January 27, 2009
Benefits of intensive insulin therapy on neuromuscular complications in routine daily critical care practice: a retrospective studyGreet Hermans, Maarten Schrooten, Philip Van Damme, et al.Human Molecular Genetics|April 29, 2017
Progranulin functions as a cathepsin D chaperone to stimulate axonal outgrowth in vivoSander Beel, Matthieu Moisse, Markus Damme, et al.The Journal of Rheumatology|January 6, 2004
Etanercept in the treatment of patients with primary Sjögren's syndrome: a pilot studyMichiel M Zandbelt, Peter de Wilde, Philip van Damme, et al.Molecular Neurodegeneration|October 18, 2018
Progranulin reduces insoluble TDP-43 levels, slows down axonal degeneration and prolongs survival in mutant TDP-43 miceSander Beel, Sarah Herdewyn, Raheem Fazal, et al.Neuromuscular Disorders : NMD|February 1, 2016
How robust is ACTIVLIM for the follow-up of activity limitations in patients with neuromuscular diseases?Charles Sèbiyo Batcho, Peter Y K Van den Bergh, Philip Van Damme, et al.Plos One|October 23, 2010
Progranulin is neurotrophic in vivo and protects against a mutant TDP-43 induced axonopathyAngela S Laird, Annelies Van Hoecke, Louis De Muynck, et al.Human Molecular Genetics|February 1, 2013
Hdac6 deletion delays disease progression in the SOD1G93A mouse model of ALSInes Taes, Mieke Timmers, Nicole Hersmus, et al.Neurobiology of Aging|February 3, 2009
VEGF protects motor neurons against excitotoxicity by upregulation of GluR2Elke Bogaert, Philip Van Damme, Koen Poesen, et al.European Journal of Nuclear Medicine and Molecular Imaging|December 21, 2025
Support vector machine classification of 18F-FDG PET scans across subtypes of amyotrophic lateral sclerosisChunmeng Tang, Juliette Foucher, Linn Öijerstedt, et al.Pageof 30