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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 28, 2015
Eye-tracking in amyotrophic lateral sclerosis: A longitudinal study of saccadic and cognitive tasksMalcolm Proudfoot, Ricarda A L Menke, Rakesh Sharma, et al.Human Molecular Genetics|September 27, 2013
Chondrolectin affects cell survival and neuronal outgrowth in in vitro and in vivo models of spinal muscular atrophyJames N Sleigh, Antón Barreiro-Iglesias, Peter L Oliver, et al.JMIR Research Protocols|June 4, 2026
The Motor Neuron Disease Register for England, Wales, and Northern Ireland: Protocol for a Population RegisterAndrea Biondi, Elizabeth Gray, Modupe Aggreh, et al.Human Molecular Genetics|October 24, 2019
Neuronal over-expression of Oxr1 is protective against ALS-associated mutant TDP-43 mislocalisation in motor neurons and neuromuscular defects in vivoMatthew G Williamson, Mattéa J Finelli, James N Sleigh, et al.Stem Cell Reports|April 25, 2020
Impairment of Mitochondrial Calcium Buffering Links Mutations in C9ORF72 and TARDBP in iPS-Derived Motor Neurons from Patients with ALS/FTDRuxandra Dafinca, Paola Barbagallo, Lucy Farrimond, et al.Neurology|April 18, 2018
Increased cerebral functional connectivity in ALS: A resting-state magnetoencephalography studyMalcolm Proudfoot, Giles L Colclough, Andrew Quinn, et al.Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|February 6, 2014
T₂-weighted MRI detects presymptomatic pathology in the SOD1 mouse model of ALSMatthew C Evans, Sébastien Serres, Alexandre A Khrapitchev, et al.Annals of Neurology|October 28, 2015
Vascular Defects and Spinal Cord Hypoxia in Spinal Muscular AtrophyEilidh Somers, Robert D Lees, Katie Hoban, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 24, 2017
Genetic screening in sporadic ALS and FTDMartin R Turner, Ammar Al-Chalabi, Adriano Chio, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 6, 2014
Autosomal dominant inheritance of rapidly progressive amyotrophic lateral sclerosis due to a truncation mutation in the fused in sarcoma (FUS) geneLouisa Kent, Thomas N Vizard, Bradley N Smith, et al.Pageof 23