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Neurobiology of Aging|August 11, 2012
VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patientMarka van Blitterswijk, Michael A van Es, Max Koppers, et al.Neurobiology of Aging|February 15, 2012
Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patientsMarka van Blitterswijk, Anna Blokhuis, Michael A van Es, et al.Neurogenetics|May 10, 2008
ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxiaSascha Vermeer, Rowdy P P Meijer, Benjamin J Pijl, et al.Journal of Alzheimer'S Disease : JAD|September 24, 2016
Tau Rather than TDP-43 Proteins are Potential Cerebrospinal Fluid Biomarkers for Frontotemporal Lobar Degeneration Subtypes: A Pilot StudyH Bea Kuiperij, Alexandra A M Versleijen, Marijke Beenes, et al.Plos One|November 17, 2012
Genetic overlap between apparently sporadic motor neuron diseasesMarka van Blitterswijk, Lotte Vlam, Michael A van Es, et al.Brain : a Journal of Neurology|July 19, 2023
SCN1A-deficient excitatory neuronal networks display mutation-specific phenotypesEline J H van Hugte, Elly I Lewerissa, Ka Man Wu, et al.Journal of Neuropathology and Experimental Neurology|November 26, 2010
Microglial upregulation of progranulin as a marker of motor neuron degenerationThomas Philips, Louis De Muynck, Hoai Nguyen Thi Thu, et al.Neurobiology of Aging|November 29, 2011
UNC13A is a modifier of survival in amyotrophic lateral sclerosisFrank P Diekstra, Paul W J van Vught, Wouter van Rheenen, et al.European Journal of Human Genetics : EJHG|February 28, 2013
Rapidly deteriorating course in Dutch hereditary spastic paraplegia type 11 patientsSusanne T de Bot, Rogier C Burggraaff, Johanna C Herkert, et al.Archives of Neurology|November 11, 2009
Survival profiles of patients with frontotemporal dementia and motor neuron diseaseWilliam T Hu, Harro Seelaar, Keith A Josephs, et al.Pageof 6