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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|January 22, 2019
Cerebellar tract alterations in PLS and ALSSicong Tu, Ricarda A L Menke, Kevin Talbot, et al.Brain and Behavior|November 6, 2024
The Basis of Cognitive and Behavioral Dysfunction in Amyotrophic Lateral SclerosisAlexander Bampton, Caroline McHutchison, Kevin Talbot, et al.Human Molecular Genetics|December 26, 2013
Neuromuscular junction maturation defects precede impaired lower motor neuron connectivity in Charcot-Marie-Tooth type 2D miceJames N Sleigh, Stuart J Grice, Robert W Burgess, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 28, 2018
Regional thalamic MRI as a marker of widespread cortical pathology and progressive frontotemporal involvement in amyotrophic lateral sclerosisSicong Tu, Ricarda A L Menke, Kevin Talbot, et al.Human Molecular Genetics|December 22, 2005
A mutation in the small heat-shock protein HSPB1 leading to distal hereditary motor neuronopathy disrupts neurofilament assembly and the axonal transport of specific cellular cargoesSteven Ackerley, Paul A James, Arran Kalli, et al.Journal of the Neurological Sciences|November 3, 2009
Head and other physical trauma requiring hospitalisation is not a significant risk factor in the development of ALSMartin R Turner, Julie Abisgold, David G R Yeates, et al.Practical Neurology|January 14, 2022
Genetic testing in motor neurone diseaseThanuja Dharmadasa, Jakub Scaber, Evan Edmond, et al.Neurology|January 18, 2013
Whole-brain magnetic resonance spectroscopic imaging measures are related to disability in ALSCharlotte J Stagg, Steven Knight, Kevin Talbot, et al.Acta Neuropathologica|April 11, 2014
FTLD-ALS of TDP-43 type and SCA2 in a family with a full ataxin-2 polyglutamine expansionDirk Bäumer, Simon Z East, Bing Tseu, et al.Practical Neurology|July 6, 2019
Tracheostomy in motor neurone diseaseMartin R Turner, Christina Faull, Christopher J McDermott, et al.Pageof 24