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Acta Neuropathologica|February 5, 2014
The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotypeJohnathan Cooper-Knock, Pamela J Shaw, Janine KirbyBrain : a Journal of Neurology|November 15, 2019
Disrupted glycosylation of lipids and proteins is a cause of neurodegenerationTobias Moll, Pamela J Shaw, Johnathan Cooper-KnockBrain : a Journal of Neurology|March 14, 2023
Physical activity as an exogenous risk factor for amyotrophic lateral sclerosis: a review of the evidenceLaura Chapman, Johnathan Cooper-Knock, Pamela J ShawNeurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 4, 2015
The Spectrum of C9orf72-mediated Neurodegeneration and Amyotrophic Lateral SclerosisJohnathan Cooper-Knock, Janine Kirby, Robin Highley, et al.Nature Reviews. Neurology|August 15, 2012
Gene expression profiling in human neurodegenerative diseaseJohnathan Cooper-Knock, Janine Kirby, Laura Ferraiuolo, et al.Essays in Biochemistry|October 8, 2021
Membrane lipid raft homeostasis is directly linked to neurodegenerationTobias Moll, Jack N G Marshall, Nikita Soni, et al.Plos One|January 30, 2014
Comparison of blood RNA extraction methods used for gene expression profiling in amyotrophic lateral sclerosisNadhim Bayatti, Johnathan Cooper-Knock, Joanna J Bury, et al.Molecular Neurodegeneration|April 10, 2013
Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisationVladimir L Buchman, Johnathan Cooper-Knock, Natalie Connor-Robson, et al.Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|May 11, 2011
The use of subcutaneous glycopyrrolate in the management of sialorrhoea and facilitating the use of non-invasive ventilation in amyotrophic lateral sclerosisJohnathan Cooper-Knock, Sam H Ahmedzai, Pamela ShawNeuropathology and Applied Neurobiology|June 23, 2015
Motor neurone disease/amyotrophic lateral sclerosis associated with intermediate-length CAG repeat expansions in Ataxin-2 does not have 1C2-positive polyglutamine inclusionsJohn Robin Highley, Alejandro Lorente Pons, Johnathan Cooper-Knock, et al.Pageof 40