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Expert Review of Proteomics|November 11, 2021
Advancing mechanistic understanding and biomarker development in amyotrophic lateral sclerosisAlexander G Thompson, Patrick Oeckl, Emily Feneberg, et al.Annals of Neurology|October 30, 2025
Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Have Distinct Prediagnostic Blood Biochemical ProfilesChristos V Chalitsios, Jiali Gao, Carol A C Coupland, et al.Cell Reports|March 19, 2020
Mice Carrying ALS Mutant TDP-43, but Not Mutant FUS, Display In Vivo Defects in Axonal Transport of Signaling EndosomesJames N Sleigh, Andrew P Tosolini, David Gordon, et al.Plos One|December 25, 2013
An eye-tracking version of the trail-making testStephen L Hicks, Rakesh Sharma, Amad N Khan, et al.Cell Stem Cell|January 7, 2022
Human stem cell models of neurodegeneration: From basic science of amyotrophic lateral sclerosis to clinical translationElisa Giacomelli, Björn F Vahsen, Elizabeth L Calder, et al.Neurogenetics|February 24, 2017
ADCY5-related dyskinesia presenting as familial myoclonus-dystoniaAndrew G L Douglas, Gaia Andreoletti, Kevin Talbot, et al.Disease Models & Mechanisms|August 4, 2017
Therapeutic strategies for spinal muscular atrophy: SMN and beyondMelissa Bowerman, Catherina G Becker, Rafael J Yáñez-Muñoz, et al.Human Molecular Genetics|May 15, 2015
Dominant, toxic gain-of-function mutations in gars lead to non-cell autonomous neuropathologyStuart J Grice, James N Sleigh, William W Motley, et al.Journal of Neurochemistry|October 12, 2011
HspB8 mutation causing hereditary distal motor neuropathy impairs lysosomal delivery of autophagosomesAlice S Kwok, Kanchan Phadwal, Bradley J Turner, et al.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.Pageof 23