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Brain Communications|October 23, 2024
Dynactin-1 mediates rescue of impaired axonal transport due to reduced mitochondrial bioenergetics in amyotrophic lateral sclerosis motor neuronsRuxandra Dafinca, Carlota Tosat-Bitrian, Emily Carroll, et al.
Annals of Neurology|September 17, 2014
Quantifying disease progression in amyotrophic lateral sclerosisNeil G Simon, Martin R Turner, Steve Vucic, 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.
Plos One|August 19, 2014
Voxel-based MRI intensitometry reveals extent of cerebral white matter pathology in amyotrophic lateral sclerosisViktor Hartung, Tino Prell, Christian Gaser, 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.
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.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 1, 2024
Improving the measurement properties of the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFRS-R): deriving a valid measurement total for the calculation of changeCarolyn A Young, Amina Chaouch, Christopher J Mcdermott, et al.
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