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Human Brain Mapping|October 3, 2025
Divergent Brain Network Activity in Asymptomatic C9orf72 and SOD1 Variant Carriers Compared With Established Amyotrophic Lateral SclerosisMichael Trubshaw, Chetan Gohil, Evan Edmond, et al.Toxins|October 24, 2020
Neurotrophic Properties of C-Terminal Domain of the Heavy Chain of Tetanus Toxin on Motor Neuron DiseaseMireia Herrando-Grabulosa, Caty Casas, Kevin Talbot, et al.Nature Reviews. Neurology|February 10, 2018
Advances in therapy for spinal muscular atrophy: promises and challengesEwout J N Groen, Kevin Talbot, Thomas H GillingwaterNeurobiology of Disease|August 18, 2020
An ALS-linked mutation in TDP-43 disrupts normal protein interactions in the motor neuron response to oxidative stressEmily Feneberg, David Gordon, Alexander G Thompson, et al.Annals of Neurology|October 21, 2016
Psychiatric disorders prior to amyotrophic lateral sclerosisMartin R Turner, Raph Goldacre, Kevin Talbot, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 11, 2011
Cardiovascular fitness as a risk factor for amyotrophic lateral sclerosis: indirect evidence from record linkage studyMartin R Turner, Clare Wotton, Kevin Talbot, et al.Human Molecular Genetics|December 17, 2009
Dismutase-competent SOD1 mutant accumulation in myelinating Schwann cells is not detrimental to normal or transgenic ALS model miceBradley J Turner, Steven Ackerley, Kay E Davies, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 12, 2015
Cerebrovascular injury as a risk factor for amyotrophic lateral sclerosisMartin R Turner, Raph Goldacre, Kevin Talbot, et al.Brain : a Journal of Neurology|November 15, 2011
Integration of structural and functional magnetic resonance imaging in amyotrophic lateral sclerosisGwenaëlle Douaud, Nicola Filippini, Steven Knight, et al.Neurobiology of Disease|April 1, 2009
Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse modelBradley J Turner, Nicholas J Parkinson, Kay E Davies, et al.Pageof 23